JPH03207796A - Liquid cleanser composition for garment - Google Patents
Liquid cleanser composition for garmentInfo
- Publication number
- JPH03207796A JPH03207796A JP2004224A JP422490A JPH03207796A JP H03207796 A JPH03207796 A JP H03207796A JP 2004224 A JP2004224 A JP 2004224A JP 422490 A JP422490 A JP 422490A JP H03207796 A JPH03207796 A JP H03207796A
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- weight
- alkyl
- group
- detergent
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
- C11D3/3742—Nitrogen containing silicones
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
Landscapes
- 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)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Detergent Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、衣料用液体洗浄剤組或物に関し、更に詳しく
は衣類の縮み防止性(フエルト収縮防止性)に優れ、し
かもすすぎ性の良好な軽質の衣料用液体洗浄剤組成物に
関する.
〔従来の技術及びその課題〕
ウール製品、絹製品等の繊細な衣料は、生地を傷めない
ように軽質の洗剤を使用して手洗いで、あるいは弱い機
械力をかけて洗濯されている。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a liquid detergent assembly for clothing, and more specifically, to a liquid detergent assembly for clothing, which has excellent shrinkage prevention properties (felt shrinkage prevention properties) and good rinsability. This invention relates to a lightweight liquid detergent composition for clothing. [Prior art and its problems] Delicate clothing such as wool products and silk products are washed by hand using a light detergent or by applying weak mechanical force to avoid damaging the fabric.
しかし、これらの衣料中でも特にウール製品はぬるま湯
中で軽くもみ洗い又は押し洗いする等の細心の注意を払
ってもなお縮む傾向(フエルト収縮)があることは日常
よく経験するところである.
従来、この種の軽質洗剤にはポリオキシェチレンアルキ
ルエーテル、ポリオキシェチレンアルキルエーテル硫酸
塩、アルキルベンゼンスルホン酸塩等が主洗浄基剤とし
て広く使われている.
近年、アルキルサッカライド系界面活性剤が皮膚刺激性
が少なく、起泡性を有しているので軽質洗剤用の洗浄基
剤として注目されつつある.例えば特開昭63−501
641号公報にはアルキルグリコシドと帯電防止第4級
アンモニウム界面活性剤を含有する細線生地用洗剤組底
物が、特開昭63−501642号公報にはアルキルグ
リコシドと帯電防止アξンオキシドを含有する細繊生地
用洗剤組底物が通常のポリオキシエチレンアルキルエー
テルを使用した場合よりも良好な帯電防止性を付与でき
ることが記載されている。また、特開昭64〜6969
5号公報にはアルキルグリコシドと両性界面活性剤を併
用した洗剤組成物が、特公平1 −168613号公報
にはアルキルグリコシドとリン酸エステル系界面活性剤
を併用した洗剤組或物がそれぞれ洗浄力、起泡力、泡切
れ性が良好であることが記載されている。更に、特開昭
59 − 25896号公報には8LB 5〜14のプ
ニオン界面活性剤とアルキルグリコシドとジ長鎖型第4
級アンモニウム塩を含有する洗剤組或物が粒状汚れの除
去効果に優れており、かつ柔軟性、帯電防止性を付与で
きることが記載されている。However, it is a common daily experience that among these types of clothing, wool products in particular have a tendency to shrink (felt shrinkage) even when careful care is taken, such as gently rubbing or washing them in lukewarm water. Conventionally, polyoxyethylene alkyl ether, polyoxyethylene alkyl ether sulfate, alkylbenzene sulfonate, etc. have been widely used as the main cleaning base for this type of light detergent. In recent years, alkyl saccharide surfactants have attracted attention as cleaning bases for light detergents because they are less irritating to the skin and have foaming properties. For example, JP-A-63-501
No. 641 discloses a detergent assembly for fine wire fabrics containing an alkyl glycoside and an antistatic quaternary ammonium surfactant, and JP-A-63-501642 discloses an alkyl glycoside and an antistatic amine oxide. It is described that a detergent assembly for fine fiber fabrics can provide better antistatic properties than when ordinary polyoxyethylene alkyl ether is used. Also, JP-A-64-6969
Publication No. 5 discloses a detergent composition using a combination of an alkyl glycoside and an amphoteric surfactant, and Japanese Patent Publication No. 1-168613 discloses a detergent composition using a combination of an alkyl glycoside and a phosphate ester surfactant. It is described that it has good foaming power and foam breakability. Furthermore, JP-A-59-25896 discloses 8LB 5 to 14 punion surfactants, alkyl glycosides, and di-long chain type quaternary surfactants.
It is stated that a detergent composition containing an ammonium salt has an excellent effect of removing particulate dirt, and can impart flexibility and antistatic properties.
しかしながら、これらの洗剤を使用してもウール製品の
縮みは抑制することができない。However, even with the use of these detergents, shrinkage of wool products cannot be suppressed.
本発明者らは先にカチオン性基又は三級アミノ基を有す
る、粒径がo.oos〜0.2−の微細な高分子ラテッ
クスを配合した軽質洗剤がフェルト収縮防止に著しい効
果があるこεを見出した(特開昭63 − 8492号
公報、特開昭63 − 89596号公報).
しかしながら、該高分子ラテックスはアルキルグリコシ
ド系の洗浄剤組或物には安定に配合することが雛しい。The present inventors have previously obtained particles having a cationic group or a tertiary amino group and having a particle size of o. It has been found that a light detergent containing a fine polymer latex of oos~0.2- is significantly effective in preventing felt shrinkage (Japanese Unexamined Patent Publication Nos. 8492-1982 and 89596-1983). However, it is difficult to stably incorporate the polymer latex into an alkyl glycoside detergent composition.
(課題を解決するための手段〕
本発明者らは前記!lK題を解決すべく鋭意研究の結果
、アルキルグリコシドとある種のシリコーン化合物を含
有してなる洗浄剤&IlIfi物が優れたフェルト収縮
防止効果を有し、且つ良好な起泡性を示し、しかもすす
ぎ性も改善されることを見出し本発明を完戒するに至っ
た。(Means for Solving the Problem) As a result of intensive research to solve the above-mentioned problem, the present inventors found that a cleaning agent & IlIfi product containing an alkyl glycoside and a certain type of silicone compound is excellent in preventing felt shrinkage. They found that the present invention was effective and exhibited good foaming properties, as well as improved rinsing properties, and thus completed the invention.
すなわち本発明は、
(a) アルキルグリコシド 5〜70重量%
(9)アミノ変性シリコーン又はその誘導体0.05〜
5重量%
を含有してなる衣料用液体洗浄剤ikIltc物を提供
するものである.
本発明において使用される(a) t分であるアルキル
グリコシドとしては、例えば次の一般式(I)
R+ (ORz),lGy
(1)
(式中、R+は直鎖又は分岐鎖の炭素数8〜18のアル
キル基、アルケニル基又はアルキルフェニル基、hは炭
素数2〜4のアルキレン基、Gは炭素数5又は6の還元
糖に物来する残基であり、X及びyは平均値であって、
Xは0〜5の数、yは1〜10の数である.)で表され
るものが好ましい。That is, the present invention provides: (a) alkyl glycoside 5 to 70% by weight
(9) Amino modified silicone or its derivative 0.05~
A liquid detergent for clothing containing 5% by weight of ikIltc is provided. The alkyl glycoside (a) used in the present invention is, for example, the following general formula (I) R+ (ORz),lGy (1) (wherein R+ is a linear or branched chain having 8 carbon atoms). ~18 alkyl group, alkenyl group or alkylphenyl group, h is an alkylene group having 2 to 4 carbon atoms, G is a residue derived from a reducing sugar having 5 or 6 carbon atoms, and X and y are average values. There it is,
X is a number from 0 to 5, and y is a number from 1 to 10. ) is preferred.
一般式(1)において、R,は溶解性、起泡性及び洗浄
性の点から、炭素数が9〜14であるのが好ましい。ま
た、R,は水溶性等の点から炭素数2〜3であるのが好
ましい。また、Xの値は水溶性及び結晶性を調整し、こ
れが大きいほど水溶性が高く且つ結晶性が低くなる傾向
があり、好ましい範囲は0〜2、特に0であるゆyは1
〜4の範囲にあることが好ましい。yはR1の疎水基に
由来する物性を考慮し選択するのが望ましく、例えばR
,が平均炭素数9〜11の疎水基である場合はy=t〜
1.4を、平均炭素数12〜14の疎水基である場合は
y=x.s〜4.0を選択するのが好ましい.尚、平均
糖重合度yはプロトンNMRにて求めることができる.
このII1iの結合様式は、1−2、1−3、1−4も
しくは1−6結合、α一もしくはβ−ビラノシド結合又
はフラノシド結合のいずれか又はこれらの組み合わせで
ある.
更に、Gは原料である単糖又は多糖によってその構造が
決定されるが、この単糖としては例えばグルコース、フ
ルクトース、ガラクトース、キシロース、マンノース、
リキソース、アラビノース等が、多糖としては例えばマ
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、ゲンチアノース、
メレジトース等が挙げられ、これらは単独又は2種以上
を組み合わせて使用できる.これらのうち、入手容易性
、及び低コスト性という点から、単糖類原料としてはグ
ルコース、フルクトース等が、多**原料としてはマル
トース、スクロース等が好ましい.
(a)!分は組成物中に5〜70重量%、好ましくは1
0〜40重量%配合される.
本発明に使用される(b)戒分であるアミノ変性シリコ
ーン又はその誘導体としては、例えば次の一般式(II
)で表される化合物が好ましい.〔式中、
R:炭素数1〜4のアルキル基、ヒドロキシ基又はアル
コキシ基
R,:炭素数1〜4のアルキル基であり、全て同一であ
る必要はない
AIR,又は−(CHt)−(OCzHn) h− (
OCsHi) c−ORgであり、ここで
a ;2又は3
b.c;O又は1〜30(但し共に0になることはない
)
R!:炭素数1〜24のアルキル基を示すB
R3
: −(CH*)4N X又は
であり、ここで
d.e;2〜6
R!,R.;水素原子又は炭素数1〜4のアルキル基を
示す
X :水素原子、炭素数1〜24のアルキル0
11
基又は 一C−Rs を示し、ここで
R,;炭素数1〜l8のアルキル基又は− (cut)
t− (C!840) l (C2HhO) h −
R.f ; 1〜6
g.h;0又はl〜30(但し共にoになることはない
)
Rh;炭素数1〜18のアルキル基
を表す.
(XがH又は炭素数1〜4のアルキル基の場合には1ヶ
又は2ヶの窒素原子は4級化されていてもよい)〕
上記一般式(II)
で表されるシリコーン化合
Rs Ra
0
11
Xが炭素数1〜24のアルキル基又は−c−psである
化合物が好ましい.
上記一般式(II)で表されるシリコーン化合物の分子
量は2000〜150000、ア藁ン当量は1000〜
20000の範囲が好ましく、閣,nはこれらに対応す
る数である.
(b)戒分は組威物中に0.05〜5重量%、好ましく
は0.1〜3重量%配合される。In general formula (1), R preferably has 9 to 14 carbon atoms from the viewpoint of solubility, foaming properties, and detergency. Further, R, preferably has 2 to 3 carbon atoms from the viewpoint of water solubility. In addition, the value of
It is preferable that it is in the range of ~4. It is desirable to select y in consideration of the physical properties derived from the hydrophobic group of R1, for example, R
, is a hydrophobic group having an average carbon number of 9 to 11, then y=t~
1.4 is a hydrophobic group having an average carbon number of 12 to 14, y=x. It is preferable to select s~4.0. Note that the average degree of sugar polymerization y can be determined by proton NMR. The binding mode of II1i is any one of 1-2, 1-3, 1-4 or 1-6 bonds, α- or β-viranoside bonds, or furanoside bonds, or a combination thereof. Furthermore, the structure of G is determined by the monosaccharide or polysaccharide that is the raw material, and examples of this monosaccharide include glucose, fructose, galactose, xylose, mannose,
Lyxose, arabinose, etc., and polysaccharides such as maltose, xylobiose, isomaltose, cellobiose, gentibiose, lactose, sucrose, nigerose, turanose, raffinose, gentianose,
Examples include melezitose, which can be used alone or in combination of two or more. Among these, from the viewpoint of availability and low cost, glucose, fructose, etc. are preferable as monosaccharide raw materials, and maltose, sucrose, etc. are preferable as polysaccharide raw materials. (a)! 5 to 70% by weight, preferably 1% by weight in the composition.
Contains 0 to 40% by weight. The amino-modified silicone or derivative thereof used in the present invention (b) is, for example, the following general formula (II
) are preferred. [In the formula, R: an alkyl group having 1 to 4 carbon atoms, a hydroxy group, or an alkoxy group R: an alkyl group having 1 to 4 carbon atoms, which do not necessarily have to be the same AIR, or -(CHt)-( OCzHn) h- (
OCsHi) c-ORg, where a; 2 or 3 b. c; O or 1 to 30 (however, both cannot be 0) R! : Represents an alkyl group having 1 to 24 carbon atoms. R3 : -(CH*)4N X or, where d. e; 2~6 R! ,R. ; Represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms; X represents a hydrogen atom, an alkyl group having 1 to 24 carbon atoms, or 1C-Rs, where R; Or- (cut)
t- (C!840) l (C2HhO) h -
R. f; 1-6 g. h; 0 or 1 to 30 (however, both are not o); Rh; represents an alkyl group having 1 to 18 carbon atoms. (When X is H or an alkyl group having 1 to 4 carbon atoms, one or two nitrogen atoms may be quaternized)] Silicone compound Rs Ra represented by the above general formula (II) 0 11 Compounds in which X is an alkyl group having 1 to 24 carbon atoms or -c-ps are preferred. The molecular weight of the silicone compound represented by the above general formula (II) is 2,000 to 150,000, and the straw equivalent is 1,000 to 1,000.
A range of 20,000 is preferred, and n is a number corresponding to these. (b) The ingredient is blended in the composition in an amount of 0.05 to 5% by weight, preferably 0.1 to 3% by weight.
なお、従来ジメチルボリシロキサンに代表されるシリコ
ーン化合物は泡調節剤として洗剤に微量配合できること
は一般に知られている.また、特開昭60 − 215
099号公報にはアミノ変性シリコーン又はその誘導体
を洗剤に少量配合することにより衣類に柔軟性を付与で
きることが記載されている.しかし、これらの技術はア
ルキルグリコシド系を使用した本発明の構威及び作用効
果を何ら開示ないしは示唆するものではない.
本発明組威物の残部は水であるが、他のノ二オン界面活
性剤、特にポリオキシエチレン(平均付加モル数5〜2
0)アルキル(C9〜14)エーテルをアルキルグリコ
シドに対し50重量%以下、好ましくは10〜50重量
%配合することにより本発明の効果を損なうことなく洗
浄効果を更に高めることができる.カチオン界面活性剤
の配合は望ましくない.カチオン界面活性剤はアミノ変
性シリコーンより衣類に対する吸着力が強く、そのため
アミノ変性シリコーンの吸着が阻害されると推測される
からである。アニオン性、両性界面活性剤は少量(組威
物中5重量%以下、好ましくは1重量%以下)であれば
配合可能である.
本発明m或物にはこの種の軽質洗剤に配合される他の任
意或分を配合することができる.このような任意威分と
して、ポリアクリル酸、ポリビニルビロリドン、ボリエ
チレングリコール、カルボキシメチルセルロース等の再
汚染防止剤:ブロテアーゼ、アミラーゼ、リパーゼ、セ
ルラーゼ等の酵素;塩化カルシウム等の酵素安定化剤:
エタノール等の低級アルコール;ベンゼンスルホン酸塩
、p一トルエンスルホン酸塩等の低級アルキルベンゼン
スルホン酸塩;ブロビレングリコール等のグリコール頻
:安息香酸塩、尿素等の可溶化剤;t−プチルヒドロキ
シトルエン、ジスチレン化クレゾール等の酸化防止剤;
その他蛍光染料、青味付剤、香料、抗菌剤等が挙げられ
る。It is generally known that silicone compounds, typified by dimethylborisiloxane, can be incorporated into detergents in small amounts as foam regulators. Also, JP-A-60-215
Publication No. 099 describes that flexibility can be imparted to clothing by incorporating a small amount of amino-modified silicone or its derivatives into detergent. However, these techniques do not disclose or suggest the structure and effects of the present invention using an alkyl glycoside system. The remainder of the composition of the present invention is water, but other nonionic surfactants, especially polyoxyethylene (average number of added moles of 5 to 2
0) The cleaning effect can be further enhanced without impairing the effects of the present invention by blending the alkyl (C9-14) ether in an amount of 50% by weight or less, preferably 10 to 50% by weight, based on the alkyl glycoside. It is undesirable to include cationic surfactants. This is because cationic surfactants have a stronger adsorption power to clothing than amino-modified silicones, and it is therefore presumed that the adsorption of amino-modified silicones is inhibited. Anionic and amphoteric surfactants can be incorporated in small amounts (5% by weight or less, preferably 1% by weight or less in the composition). The product of the present invention may contain other optional components that are commonly used in light detergents of this type. Such optional agents include recontamination inhibitors such as polyacrylic acid, polyvinylpyrrolidone, polyethylene glycol, and carboxymethyl cellulose; enzymes such as brotease, amylase, lipase, and cellulase; enzyme stabilizers such as calcium chloride;
Lower alcohols such as ethanol; lower alkylbenzenesulfonates such as benzenesulfonates and p-toluenesulfonates; glycols such as brobylene glycol; solubilizers such as benzoates and urea; t-butylated hydroxytoluene, Antioxidants such as distyrenated cresol;
Other examples include fluorescent dyes, blue tints, fragrances, and antibacterial agents.
また、本発明組威物は通常の洗剤ビルダー或分を実質上
含まないことが望ましいが、ジグリコール酸塩、リン酸
塩、炭酸塩等のビルダー或分を2〜3重量%以下であれ
ば配合することもできる。Further, it is desirable that the composition of the present invention does not substantially contain a certain amount of ordinary detergent builders, but as long as the amount of builders such as diglycolate, phosphate, carbonate, etc. is 2 to 3% by weight or less. It can also be blended.
以下、実施例を挙げて本発明を更に具体的に説明するが
、本発明はこれらの実施例に限定されるものではない。EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these Examples.
実施例1
(1)フェルト収縮率及び面積収縮率の測定(1)供試
布の調製
三方をロックミシンでかがった、大きさlOXIOCI
Iのウールの未加工布を、常温の水道水に30分間浸漬
後、脱水槽にて30秒間脱水し、綱の上に載せて平干し
し、20℃、65%Rliで4時間以上調湿した.この
布に油性のサインベンで4カ所印を付け、それぞれに番
号を付した後、それぞれの印の間の長さを測定し(タテ
a+’+az”;ヨコbt”,bx’)、この長さを原
長とした.
(2)洗濯方法
ターグー〇=トメーター(Terg−0−↑osete
r,上島製作所製)を用い、(1)で得た供試布3枚を
1つのボントに入れ、12O r.p.m.で10分間
回転させて洗濯を行った。各洗剤濃度は0.25重量%
とし、水温は20゜Cとした.すすぎとしては、一回目
はポット中の流水すすぎ、二回目は手洗い桶中の流水す
すぎを行った.次いで、この供試布を洗濯機の脱水槽の
壁につけて30秒間脱水後、綱の上にのせて平干しして
乾燥させ、20℃、65%RHで4時間以上調湿した.
更に、先に(1)で付した印について再度それらの間の
長さを測定し(タテal’+ aK’ ;ヨコb.’,
bz’) 、これから次式に従ってフエルト収縮率及
び面積収縮率を算出した。この結果を第1表に示す.
〈収縮率の算出(INS TM9より)〉R.M. :
洗濯前の測定値(原長)
11.L :洗濯後の測定値
く面積収縮率の算出〉
w.s.x t,s.
面積収縮率(%) =W,S.+L.S.100
W.S. :横方向のフエルト収縮率
L.S. :縦方向のフェルト収縮率
〔■〕泡立ち及びすすぎ性の評価
101!のたらいに30℃の水道水51を入れ、ウール
未加工布及びアクリルジャージをそれぞれ100gずつ
合計200g、並びに洗剤12.5mを投入した.5分
間洗濯した後、布を脱水機により30秒間脱水後、30
℃の水道水5lを入れ、1分間押し洗いすすぎをした.
洗濯5分後の泡立ちの高さ(C11)及び押し洗いすす
ぎl分後の泡の量を肉眼で下記基準により評価した.
すすぎ指数;
5:液面全体に泡が残る
4:液面Xに泡が残る
3:液面2に泡が残る
2:液面に細かい泡が残る
1:液面に泡がない
アルキルグリコシド(l);
一般式(1)において
R, x=C,−, 、、x−0, y −1.35、
G:グルコース残基
アルキルグリコシド(2);
一般式(1)において
R I= C 1t、x=0,y=1.7、G;グルコ
ース残基
シリコーン(1):
一般式(If)において
R, R+, A :CHa
B : − (CH2) 3−Nll− CCHt)
z−NH−C− (CHI) 3− (C![140)
4−CIH . ,l1
0
分子量14000、アミン当量4500シリコーン(2
):
一般式(If)において
R, Rl, A :CH3
B : − (CL) 3−NH− (CHz)つ−N
il−C−CI Jzx11
分子置20000、アミン当量100(1シリコーン(
3):
一般式(II)において
R, Rl+ A :CHx
B : − (CHz) s−Nll− (CL)−N
u−C+ tubs分子量7000、アミン当量230
0
シリコーン(4):ジメチルボリシロキサン分子量10
000 、アξン当量O
?施例2
第2表に示す戒分組威の各種洗浄剤組威物を調製し、そ
れぞれの洗浄力を下記の方法によって評価した.尚、ア
ルキルグリコシド(1)及びシリコーン(1)は実施例
1で用いたものと同じものである.
2(こ■11がJ乱製
*汚れの組成
カーボンブラック 15%綿実油
60%コレステロール
5%
オレイン酸 5%
バルミチン# 5%
液体バラフィン 10%上記組威物1k
gを801のバークレンに溶解分散し、金巾2023布
を浸漬して汚れを付着させた後、バークレンを乾燥除去
する.
゛び
評価用洗剤水溶液1lに103X10CIIの綿の皮脂
/カーボン汚れ汚染布(人工汚染布)を各5枚入れ、タ
ーゴトメーターにて10Or.p4,で次の条件で洗浄
した.洗浄条件は次の通り.〈洗浄条件〉
洗浄時間 3分
洗浄濃度 0.25%
水の硬度 4゜
水 温 30℃
すすぎ 水道水にて5分間
洗浄力は汚染前の原布及び洗浄前後の汚染布の460V
における反射率を自記色彩計(島津製作所)
にて測定し、
次式によって洗浄率
(%)
を求めた
(表には5枚の測定平均値を
示す)
第
2
表
注)
ネ
:バランス量の略Example 1 (1) Measurement of felt shrinkage rate and area shrinkage rate (1) Preparation of sample fabric Sewn on three sides with lock sewing machine, size 1OXIOCI
The unprocessed wool cloth of I was immersed in tap water at room temperature for 30 minutes, dehydrated for 30 seconds in a dehydration tank, placed on a rope to dry flat, and conditioned at 20°C and 65% Rli for over 4 hours. did. Mark four places on this cloth with an oil-based sign marker, number each one, measure the length between each mark (vertical a+'+az"; horizontal bt", bx'), and measure this length. is the original length. (2) Washing method Terg-0-↑osete
R, manufactured by Uejima Seisakusho), the three test fabrics obtained in (1) were placed in one bong, and heated at 12 O r. p. m. I washed it by spinning it for 10 minutes. Each detergent concentration is 0.25% by weight
The water temperature was 20°C. For rinsing, the first rinse was done with running water in a pot, and the second time was with running water in a hand washing tub. Next, this sample fabric was applied to the wall of the dehydration tank of a washing machine to dehydrate it for 30 seconds, then placed on a rope to dry flat, and the humidity was controlled at 20° C. and 65% RH for over 4 hours. Furthermore, the length between the marks made in (1) was measured again (vertical al'+aK'; horizontal b.',
bz'), from which the felt shrinkage rate and area shrinkage rate were calculated according to the following equations. The results are shown in Table 1. <Calculation of shrinkage rate (from INS TM9)> R. M. :
Measurement value before washing (original length) 11. L: Calculation of area shrinkage rate based on measured value after washing> w. s. xt, s. Area shrinkage rate (%) = W, S. +L. S. 100 W. S. : Horizontal felt shrinkage rate L. S. : Vertical felt shrinkage rate [■] Foaming and rinsability evaluation 101! 51 g of tap water at 30°C was placed in a basin, and 200 g of unprocessed wool cloth and 100 g of acrylic jersey each, and 12.5 m of detergent were added. After washing for 5 minutes, spin the cloth in a dehydrator for 30 seconds, then
I poured 5 liters of tap water at ℃ and rinsed it for 1 minute. The height of foaming (C11) after 5 minutes of washing and the amount of foam after 1 minute of washing and rinsing were evaluated with the naked eye according to the following criteria. Rinse index; 5: Bubbles remain on the entire liquid surface 4: Bubbles remain on liquid surface l); In general formula (1), R, x=C,-, , x-0, y-1.35,
G: Glucose residue alkyl glycoside (2); In general formula (1), R I = C 1t, x = 0, y = 1.7, G; Glucose residue silicone (1): In general formula (If), R , R+, A: CHa B: - (CH2) 3-Nll- CCHt)
z-NH-C- (CHI) 3- (C! [140)
4-CIH. , l1 0 Molecular weight 14000, amine equivalent weight 4500 Silicone (2
): In the general formula (If), R, Rl, A: CH3 B: - (CL) 3-NH- (CHz) -N
il-C-CI Jzx11 Molecular position 20000, amine equivalent 100 (1 silicone (
3): In general formula (II), R, Rl+ A: CHx B: - (CHz) s-Nll- (CL)-N
u-C+ tubes molecular weight 7000, amine equivalent 230
0 Silicone (4): dimethylborisiloxane molecular weight 10
000, ξ an equivalent O? Example 2 Various detergent combinations of Kaibun-Kumii shown in Table 2 were prepared, and the cleaning power of each was evaluated by the following method. Note that alkyl glycoside (1) and silicone (1) are the same as those used in Example 1. 2 (11 is J-made *Stain composition Carbon black 15% cottonseed oil
60% cholesterol
5% Oleic acid 5% Valmitin # 5% Liquid paraffin 10% Above combination 1k
g is dissolved and dispersed in 801 Berkrene, dipped in a gold cloth 2023 cloth to adhere dirt, and then the Berkrene is removed by drying. Add 5 pieces each of 103 x 10 CII cotton sebum/carbon stain contaminated cloth (artificially contaminated cloth) to 1 liter of detergent aqueous solution for evaluation, and measure 10 Or. using a tergotometer. Washed with p4 under the following conditions. The cleaning conditions are as follows. <Washing conditions> Washing time: 3 minutes Washing concentration: 0.25% Water hardness: 4° Water temperature: 30°C Rinse: 5 minutes with tap water The cleaning power is 460V for the original fabric before contamination and the contaminated fabric before and after washing.
The reflectance was measured using a self-recording colorimeter (Shimadzu Corporation), and the cleaning rate (%) was calculated using the following formula (the table shows the average value of 5 measurements). omitted
Claims (1)
ミノ変性シリコーン又はその誘導体0.05〜5重量% を含有してなる衣料用液体洗浄剤組成物。 2 アルキルグリコシドが次の一般式( I )R_1(
OR_2)_xG_y( I ) (式中、R_1は直鎖又は分岐鎖の炭素数8〜18のア
ルキル基、アルケニル基又はアルキルフェニル基、R_
2は炭素数2〜4のアルキレン基、Gは炭素数5又は6
の還元糖に由来する残基であり、x及びyは平均値であ
って、xは0〜5の数、yは1〜10の数である。) で表されるものである請求項1記載の衣料用液体洗浄剤
組成物。 3 更にポリオキシエチレン(平均付加モル数5〜20
)アルキル(炭素数9〜14)エーテルをアルキルグリ
コシドに対し10〜50重量%含有してなる請求項1又
は2記載の衣料用液体洗浄剤組成物。[Scope of Claims] 1. A liquid detergent composition for clothing, comprising (a) 5 to 70% by weight of an alkyl glycoside, and (b) 0.05 to 5% by weight of an amino-modified silicone or its derivative. 2 Alkyl glycoside has the following general formula (I)R_1(
OR_2)_xG_y(I) (wherein, R_1 is a linear or branched alkyl group having 8 to 18 carbon atoms, an alkenyl group, or an alkylphenyl group, R_
2 is an alkylene group having 2 to 4 carbon atoms, and G is an alkylene group having 5 or 6 carbon atoms.
x and y are average values, x is a number from 0 to 5, and y is a number from 1 to 10. ) The liquid detergent composition for clothing according to claim 1, which is represented by: 3 Furthermore, polyoxyethylene (average number of added moles 5 to 20
3. The liquid detergent composition for clothing according to claim 1, which contains 10 to 50% by weight of alkyl (9 to 14 carbon atoms) ether based on the alkyl glycoside.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004224A JPH06102796B2 (en) | 1990-01-10 | 1990-01-10 | Liquid detergent composition for clothing |
| MYPI91000023A MY107192A (en) | 1990-01-10 | 1991-01-08 | Liquid detergent composition for clothes. |
| EP91100209A EP0439019A1 (en) | 1990-01-10 | 1991-01-08 | liquid detergent composition for clothes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004224A JPH06102796B2 (en) | 1990-01-10 | 1990-01-10 | Liquid detergent composition for clothing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03207796A true JPH03207796A (en) | 1991-09-11 |
| JPH06102796B2 JPH06102796B2 (en) | 1994-12-14 |
Family
ID=11578619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004224A Expired - Lifetime JPH06102796B2 (en) | 1990-01-10 | 1990-01-10 | Liquid detergent composition for clothing |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0439019A1 (en) |
| JP (1) | JPH06102796B2 (en) |
| MY (1) | MY107192A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07509515A (en) * | 1992-07-30 | 1995-10-19 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン | Method for producing storable nonionic surfactant |
| JPH0967594A (en) * | 1995-09-01 | 1997-03-11 | Kao Corp | Detergent composition |
| JPH115904A (en) * | 1997-04-21 | 1999-01-12 | Toray Dow Corning Silicone Co Ltd | Surface modifier composition |
| JPH115903A (en) * | 1997-04-21 | 1999-01-12 | Toray Dow Corning Silicone Co Ltd | Polyoxyethylene alkyl ether fatty acid amide-modified organopolysiloxane composition |
| JP2000506209A (en) * | 1996-03-04 | 2000-05-23 | エス.シー.ジョンソン アンド サン,インコーポレーテッド | Stable aqueous silane solution for hard surface cleaning |
| JP2005206731A (en) * | 2004-01-23 | 2005-08-04 | Nicca Chemical Co Ltd | Detergent composition for dry-cleaning |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI0819258T1 (en) * | 1995-04-04 | 2002-04-30 | Novartis Ag | Extended wear ophthalmic lens |
| CN121712869A (en) | 2023-08-15 | 2026-03-20 | 赢创运营有限公司 | Improved cleaning methods |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60215099A (en) * | 1984-01-25 | 1985-10-28 | ザ、プロクタ−、エンド、ギヤンブル、カンパニ− | Liquid detergent compositon containing organic functional polysiloxane |
| JPS62133177A (en) * | 1985-11-25 | 1987-06-16 | ダウ・コ−ニング・コ−ポレ−シヨン | Method for washing fabric |
| JPS6469695A (en) * | 1987-09-09 | 1989-03-15 | Shiseido Co Ltd | Detergent composition |
| JPH01168613A (en) * | 1987-12-24 | 1989-07-04 | Shiseido Co Ltd | Detergent composition |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3365810D1 (en) * | 1982-05-10 | 1986-10-09 | Procter & Gamble | Low phosphate laundry detergent compositions |
| DE3542725A1 (en) * | 1985-12-03 | 1987-06-04 | Hoffmann Staerkefabriken Ag | LAUNDRY TREATMENT AGENT |
| US4911852A (en) * | 1988-10-07 | 1990-03-27 | The Procter & Gamble Company | Liquid laundry detergent with curable amine functional silicone for fabric wrinkle reduction |
-
1990
- 1990-01-10 JP JP2004224A patent/JPH06102796B2/en not_active Expired - Lifetime
-
1991
- 1991-01-08 MY MYPI91000023A patent/MY107192A/en unknown
- 1991-01-08 EP EP91100209A patent/EP0439019A1/en not_active Withdrawn
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60215099A (en) * | 1984-01-25 | 1985-10-28 | ザ、プロクタ−、エンド、ギヤンブル、カンパニ− | Liquid detergent compositon containing organic functional polysiloxane |
| JPS62133177A (en) * | 1985-11-25 | 1987-06-16 | ダウ・コ−ニング・コ−ポレ−シヨン | Method for washing fabric |
| JPS6469695A (en) * | 1987-09-09 | 1989-03-15 | Shiseido Co Ltd | Detergent composition |
| JPH01168613A (en) * | 1987-12-24 | 1989-07-04 | Shiseido Co Ltd | Detergent composition |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07509515A (en) * | 1992-07-30 | 1995-10-19 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン | Method for producing storable nonionic surfactant |
| JPH0967594A (en) * | 1995-09-01 | 1997-03-11 | Kao Corp | Detergent composition |
| JP2000506209A (en) * | 1996-03-04 | 2000-05-23 | エス.シー.ジョンソン アンド サン,インコーポレーテッド | Stable aqueous silane solution for hard surface cleaning |
| JPH115904A (en) * | 1997-04-21 | 1999-01-12 | Toray Dow Corning Silicone Co Ltd | Surface modifier composition |
| JPH115903A (en) * | 1997-04-21 | 1999-01-12 | Toray Dow Corning Silicone Co Ltd | Polyoxyethylene alkyl ether fatty acid amide-modified organopolysiloxane composition |
| JP2005206731A (en) * | 2004-01-23 | 2005-08-04 | Nicca Chemical Co Ltd | Detergent composition for dry-cleaning |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0439019A1 (en) | 1991-07-31 |
| JPH06102796B2 (en) | 1994-12-14 |
| MY107192A (en) | 1995-09-30 |
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