JPH01318089A - Detergent composition - Google Patents

Detergent composition

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Publication number
JPH01318089A
JPH01318089A JP1113612A JP11361289A JPH01318089A JP H01318089 A JPH01318089 A JP H01318089A JP 1113612 A JP1113612 A JP 1113612A JP 11361289 A JP11361289 A JP 11361289A JP H01318089 A JPH01318089 A JP H01318089A
Authority
JP
Japan
Prior art keywords
betaine
alkyl
amine oxide
detergent composition
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.)
Granted
Application number
JP1113612A
Other languages
Japanese (ja)
Other versions
JP2664474B2 (en
Inventor
Appaya Raghunath Naik
アツパヤ・ラグナス・ネイク
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.)
Unilever NV
Original Assignee
Unilever NV
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
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Application filed by Unilever NV filed Critical Unilever NV
Publication of JPH01318089A publication Critical patent/JPH01318089A/en
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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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0094High foaming 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
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic 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
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/32Amides; Substituted amides
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/146Sulfuric acid esters
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • 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

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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)
  • Cosmetics (AREA)

Abstract

PURPOSE: To provide a water-soluble liquid detergent composition having excellent foaming stability, washing ability, safety and low stimulus, by including alkyl polyglycoside surfactant, anion active agent, surface active betaine and/or amine oxide in the specified condition.
CONSTITUTION: This detergent composition is desirably formed of C8-18 alkylpolyglycoside surfactant, which has a mean degree of polymerization at 1-3, at 30-60wt.% in relation to the whole of active component, and simple betaine expressed with a formula [>>R means C8-18 alkyl, R6-7 means C1-3 (hydroxyl) alkyl], interface active betaine as amino betaine expressed with a formula II, amine oxide, which are expressed with a formula RR6R7NO, and ethanol amide to be used at need at 12-30wt.% as a total content thereof, and/or anion active agent as a first alkyl sulfate at 1.5 time mole or more of the content of the betaine and/or amine oxide, and water.
COPYRIGHT: (C)1989,JPO

Description

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

の 本発明は新規な洗剤組成物、それ専用ではないが、特に
食器の手洗い等の軽度の洗浄に有用な気泡性液体組成物
に係る。この組成物はさらに布地洗濯、カーペットのク
リーニング及びシャンプーとしても使用できる。
The present invention relates to novel detergent compositions, particularly, but not exclusively, foaming liquid compositions useful for light cleaning such as hand washing of dishes. The composition can also be used for fabric washing, carpet cleaning and shampooing.

【L匹反五二五J 軽 食器洗浄に適するようケ?質液体洗剤組成物は公知であ
る。市販されている配合物の多(は、スルフェート型か
スルホネート型のアニオン洗剤に基づき、特にアルキル
ポリエトキシスルフェート(アルキルエーテルスフエー
ト)と組合せたアルキルスルフェート、アルキルベンぜ
ンスルホネート及びアルカンスルホネートに基づくもの
である。 スルホネート型洗剤が一般に優勢である。 アルキルベンピンスルホネート/アルキルエーテルスル
フェート、又はアルキルスルフェート/アルキルエーテ
ルスルフェートに基づ〈従来型の食器洗浄液の使用が、
使用者の手荒れの原因となることが知られている。その
ため、洗剤製品の、特に食器洗浄液の低刺激性がこうし
た製品の望ましい性質となっている。 アルキルモノ−グリコシドとアルキルポリ−グリコシド
は公知であり、数多くの従来特許や刊行文献に記載され
てきた。例えばBoettner  (米国特許第32
19656号)は、アルキルモノ−グリコシドがアニオ
ン及び非イオン界面活性剤の泡安定剤として有効である
と開示している。L evt (米国特許第37722
69号)は、1.6g未満のグル」−ス・ユニットを含
むデシルグルコシドが良好な発泡イ乍 剤として發用することを開示している。 P rOcter& G ambleの幾ツかの開示(
例えば、E P  O070074号、E P  O0
70075号、E P O070076)は、洗剤組成
物中に1.5個以上のグリコース・ユニットを含むアク
リルポリグルコシドが有効であることを論じている。日
enke 1(E P 216301A ”)は、1〜
1.4個のグルコース・ユニットを有するアルキルグリ
コシドをエーテルスルフェートとエタノールアミドを含
む食器洗浄液に混合して使用するのが有効であると開示
している。 工REII(欠IL 本発明は、アルキルポリグリコシドを基剤とする、良好
な泡安定性と良好な洗浄能力をもつ安全・避 な低刺激、制2洗剤に係る。本発明は、アルキルポリグ
リコシドを含む新規な高発泡性譚イオン呈剤液体洗剤を
提供することを目的とする。更に、環境に無害で低刺激
性の液体洗剤を提供することを目的とする。 従って、本発明は以下のような水性液体洗剤組成物に係
わる。この組成物は、 (a)1〜3の平均重合度を有するC8〜018アルキ
ルポリグリ」シト界面活性剤、 (b)アニオン活性剤、 (c)界面活性ベタイン及び/又はアミンオキシド、 そして任意に、 (d)エタノールアミドを含む この組成物中、アニオン活性剤の指はベタイン及び/又
はアミンオキシドの含量の(モル基準で)1.5倍を超
えることなく、また、ベタイン及び/1幣眠嗜 全     重量%である。 アルキルポリグリコシドは本来非イオン性であるが、異
むった型の親水基を有する点で、アルキルエトキシレー
トまたはアルキルフェノールエトキシレートのような従
来のエトキシル化された非イオン剤と相違しており、従
って従来のエトキシル化された非イオン剤に比較して、
異なった物理的、化学的、機能的な特性を示す。例えば
、エトキシレートは低融点固体あるいは室温で液体であ
り、無極性溶媒中で完全に混和でき、その水溶液はDり
点を有する。それに比べて、アルキルポリグリコシドは
高融点固体であり、無極性溶媒中では溶解性に乏しく、
その水溶液は曇り点を示さない。また、類似する従来型
の非イオン剤に比べて、フルキルポリグリコシドは一般
により低い表面張力とより安定した泡をもたらす。更に
、アルキルポリグリコシドは異なった方法で製造され、
自然界の原材料だけを用いて製造可能である。従って、
アルキルポリグリ」シトから作られた化合物及び組成物
は、従来の非イオン剤とそれを含む組成物に比べて生物
学的に一層安全かつ許容可能であることが期待できる。 存在する不純物もまた従来の非イオン剤と異なるものと
なる。 アルキルポリグリコシドは、洗剤アル」−ルのF 1s
cherグリコシド化によって製造できる。例えば、 08〜C18アルコール(ROH)+rグルコース」(
G)十触媒→ROG  +H20 × ROGx生成物の詳細は反応物の比率の調整に依存する
。ある生成物は、例えば、ROGl :ROG2:RO
G3の比率となる。 本発明に使用されるアルキルポリグリコシドは、炭素原
子およそ8〜20個、好ましくは約10〜約16個、最
も好ましくは12〜14個を含む疎水基と、サツカリド
・ユニット約1〜約3個、好ましくは1〜1.5個、最
も好ましくは1.2〜1.4個を平均して含む多糖疲水
基とを有する。サツカリド・」ニットの例と1ノでは、
ガラクトシド、グルコシド、フルクトシト又はグリコジ
ルがある。これらの混合物も使用できる。 好ましいアルキルポリグリコシドは、Horizonあ
る。APG500の平均重合度は1.4であり、APG
550は1,8である。米国特許第4599188号(
L 1enadO)は、アルキルポリグリコシドについ
て更に説明と特徴づけを行っている。 アルキルポリグリコシドが主要な活性成分であることが
好ましく、例えば、活性■休の30〜60重邑%を占め
ることが好ましい。 ム二土之盾且1 本発明に従って使用される共活性アニオン界面活性剤は
、スルフェート型又はスルホネート型、又はそれらの混
合物である。スルフェートは従来のアニオン合成洗剤で
あってもよいし、アルカノール(すなわち、n=o )
あるいはエトキシル化されたアルカノール 硫酸半ニーステルであってもよい。適当なスルフェート
は、エトキシル化された、あるいはエトキシル化されて
いない線状、枝分れ、第1又は第2アルコールから得ら
れる。好ましいアルコールは以下のものである。 れている場合にはアルコール1モルにつき12モルまで
のエチレンオキシドを含む線状第1アルコール。 ( ii)  炭素原子10〜15個と2−メチル分技
亭 ( branchiho)約25%を含、エトキシル化
されている場合にはアルコール1モルにつき12モルま
でのエチレンオキシドを含む、主として直鎖状の第1ア
ルコール。 (iii )  炭素原子を11〜15個とアルコール
1モルにつき7〜30モルのエチレンオキシドを含むラ
ンダム第2アルコール。 実質的に枝分れした第1アル]−ルを使用してもよい。 アニオン界面活性剤を中和するカチオンはナトリウムと
アンモニウムが好ましく、後者のスルフェートは、本発
明の液体組成物のしドロトロープを促進することが可能
である。 スルホネートは、線状アルキルベンゼンスル小ネート、
第2アルキルスルホネート、αオレフインスルホネート
のような従来より使用されているスルホネートでよい。 アミンオキシ゛/ベタイン 本発明の第3の重要な特徴は、起泡増進剤としてのアミ
ンオキシド又はベタインの存在である。 経済性と当然の費用効果性のためには、アミンオキシド
又はベタイン、特にアミンオキシドの実質約1を使用す
ることは避けるのが好ましい。アミンオキシドの吊が活
性洗剤混合物の10重量%を超えないことが好ましい。 また、ベタインの41が本混合物の30! m%を超え
ないことが望ましい。 アミンオキシドとベタインとの合31最は、活性洗剤混
合物の12〜30重量%である。起泡増進剤は組酸物全
体の2〜6  含まれるのが好ましい。ベタインだけを
使用するのが好ましい。 適当なベタインは次式 %式% の単純ベタインと、次式 R−C0NHCHCM  CHN” CH2Co2のア
ミドベタインを含む。 cut)ココヤシアルキル基でもよい。1(6とR7は
各々C1〜C3アルキル又はC1〜C3ヒドロギシアル
キルである。スタホベタインの例は、上記の式の−CO
CO2を次の形に置き換えた式となる: −(cH2)3S03又は−CH2−Cll5II2S
o3適当な単純ベタインは、A Ibriaht & 
W 1lsonのE mpigen  B Bである。 この単純ベタインは、Rがココヤシから得られたCI2
〜C14I2率ルであり、R6とR1の両方がメチルで
あるような上記の式をもつ。他に好ましいものは、 G oldschmidtのTegOLIT”あり、こ
れは完全なRR6RIN−0 (式中、Rが直鎮又は枝分かれ鎖c−c18アルキル基
であり、R6とR7の各々がC1〜C3ア′1シ 揄キ又は01〜C3ヒドロキシアルキルである)を有す
る。適当なアミンオキシドはΔ1briot+t &W
ilsonのE mpigen  OBでありこの場合
、Rはψ 中断]コヤシアルキルであり、R6とR7の両方がメチ
ルである。 匡旌濾】 炎 本発明による組成物は、少量のビルダー、荻素、塩化ナ
トリウムもしくは塩化アンモニウム、腐蝕抑制剤、着色
剤、香料のような他の従来成分を含む。エタノールアミ
ドのような従来の起泡増進剤を含んでもよい。 エタノールアミドの添加は任意である。添加の12〜3
0重四%となるようにする。好ましいエタノールアミド
はEllpilan  LME (Albright 
&Wilson)である。 本発明による組成物は、特に手洗いによる食器洗浄の為
の軽洗浄用液体洗剤として使用される。 本文中で使用される[食δ(dishes) Jという
用語は、食品調理あるいは食品摂取に用いられるあらゆ
る用具を意味する。食品細片や他の食品残留物(油脂、
タンパク質、でんぷん、樹脂、染料、オイル、焦げた有
機物残留物)をこうした用具から取り除くために、洗浄
が必要とされる。 手洗いによる食器洗浄に用いられる典型的な組成物は、
前述の活性成分を約5〜約60重量%、好ましくは約1
0〜約40重量%含み、残りは水と溶媒とから成る組成
物である。 本発明による組成物は低刺激性で環境的に安全であり、
良好な泡特性を有する。 笈鹿上 吻ツ 様々な配合物の発泡性能と低刺激性を比較した。 本発明の適用範囲内の配合物を、本発明範囲外の同等の
組成物と比較した。 FOttCund  3 eiren  1951,5
3,207に記載の原理に基づく改良されたS chl
achter−D 1erkcs試験を用いて、発泡性
能を評価した。温度45℃で硬度24°H(フランス硬
度)の水中に活性洗剤濃度0.04%含む各々の試験材
料の水溶液100dを、垂直に振動する多孔円板を使っ
て、目盛り付きのシに、汚れ(水120部中に市販の料
理用脂肪95部、オレイン1i120.25部、ステア
リン@0゜25部、小麦でんぷん10部を含むもの)の
増加分(0,i)を、泡が消失するまで15秒間隔(緩
かな撹拌10秒と停止5秒)で加えた。汚れ増加分の数
(NSI点数)として、結果を記録された。6以トの点
数差は一般的に無意味であるとみなされる。各々の結末
は典型的に平均3〜4点であった。 界面活性剤とその混合物のタンパク質変性能力を評価す
るin vitro  あるいはin vivoの方法
の幾つかが報告されテイル(M iyazawa他、I
ntJ  Cos  Sci、  6.33〜46.1
984、及びそれに引用された論文を参照のこと)。こ
うした方法のひとつは、皮膚から得られた酸小スファク
ターゼ263〜273 、1984)または小麦ヰ弁か
ら)ミナられた同酔索(T anaka他、Anal 
3 iochem、 66.489〜498、1975
 )と洗剤との相互作用を調べることである。 イ代 配合物のin vivo−?f′刺激性はフレックス洗
浄試験(Nex wash test)を用いて評価で
きる。この罰 試験では、未希釈の製品を被験者の身腕部に塗りつけて
は洗い落した。この処置を1日につき、4回、5日間繰
り返し、皮膚に現れた紅斑の度合いを熟練した評価者が
評価した、 拳 小麦胚芽ホスファターゼ試験(WGAP)結果とフレッ
クス洗浄試験結果の比較から、試験条件下で50%未満
の酵素抑制をもたらす配合物は実質的に低刺激性である
ことを示した。フレックス洗夕 浄試験では、40未満の抑制をもたらす製品の間の低刺
激性の差異からは検知可能な差異は全く示されなかった
。この試験により、酵素試験は非常に敏感であること、
そして、実際の生活条Wイでは、そのレベル以下ではど
んな活性剤も製品も等しくY亡 低刺激性を示  ンバク質変性の限界レベルがあること
が明らかになった。WGAP試験結果は抑制%(即ち、
100%から活性%を引いた残り分)として表される。 水は全く抑制をもたらさず、即ち、100%の活性が残
った。 i皿且1 A      P      G  :     Ho
r’+zon    Chemicals    ネ1
 製APG500、または△PG550゜ 両者は012〜C14アルキル基を 有する。平均重合度は各々1.4 と 1.8t”ある。 P  A   S :  Dobanol 23−8 
(Shell)。 ベ  タ  イ  ン :    E mpioen 
  OB  (A  1briCIht  &WilS
On)。 アミンオキシド: Empiaen  OB (Alb
riaht &Wilson)。 L   M    E  :   Emplilan 
 LME  (Albriaht&W 1Ison) 試験される組成物の成分量の変化は、次の表において組
成物総重量の%で示される。 発泡試験から、本発明の範囲内の組成物は、範囲外の組
成物(A、B、D)より良好な発泡性能をもつことが明
らかである。更に、APG500はAPO550より性
能が良好である。 以下のM索抑制試験を行った。 製       口0      酵素j111シ11
%19/6/415  Dobanol 9l−8FO
/PAS/ベタイン/LH[A19/6/415  A
PG 500/PAS/ベタイン/LHE      
   4WGAP試験では、APGと非イオン性配合物
は同様に低い酵素抑制性を示し、従ってこの両者は同様
の低刺激性をもつものである。 代理人弁理士 月a  山    武
[L anti-525 J Is it suitable for cleaning the snack bowl? High quality liquid detergent compositions are known. Many of the commercially available formulations are based on anionic detergents of the sulfate or sulfonate type, especially alkyl sulfates, alkyl benzene sulfonates and alkanesulfonates in combination with alkyl polyethoxy sulfates (alkyl ether sulfates). Sulfonate-type detergents generally predominate. The use of conventional dishwashing liquids based on alkylbenpine sulfonates/alkyl ether sulfates or alkyl sulfates/alkyl ether sulfates is
It is known to cause rough hands of the user. Therefore, hypoallergenicity of detergent products, especially dishwashing liquids, has become a desirable property of such products. Alkyl mono-glycosides and alkyl poly-glycosides are known and have been described in numerous prior patents and publications. For example, Boettner (U.S. Pat. No. 32
No. 19656) discloses that alkyl mono-glycosides are effective as foam stabilizers for anionic and nonionic surfactants. L evt (U.S. Patent No. 37722
No. 69) discloses the use of decyl glucoside containing less than 1.6 g of glucose units as a good blowing agent. Some disclosures of PrOcter & Gamble (
For example, E P O070074, E P O0
No. 70075, EP 070076) discusses the effectiveness of acrylic polyglucosides containing 1.5 or more glycose units in detergent compositions. Japan enke 1 (EP 216301A”) is 1~
It is disclosed that an alkyl glycoside having 1.4 glucose units can be used effectively in a dishwashing liquid containing ether sulfate and ethanolamide. TECHNICAL FIELD The present invention relates to a safe, low-irritant, detergent based on alkyl polyglycosides, which has good foam stability and good cleaning ability. It is an object of the present invention to provide a novel highly foaming liquid detergent containing an ionizing agent.Furthermore, it is an object of the present invention to provide a liquid detergent that is harmless to the environment and has low irritation. The composition relates to an aqueous liquid detergent composition comprising: (a) a C8-018 alkyl polyglycide surfactant having an average degree of polymerization of 1 to 3; (b) an anionic surfactant; and (c) an interfacial surface active agent. In this composition comprising active betaine and/or amine oxide, and optionally (d) ethanolamide, the number of anionic active agents exceeds 1.5 times (on a molar basis) the content of betaine and/or amine oxide. Alkyl polyglycosides are non-ionic in nature, but they have different types of hydrophilic groups, such as alkyl ethoxylates or alkylphenol ethoxylates. compared to conventional ethoxylated non-ionic agents, and thus compared to conventional ethoxylated non-ionic agents.
Exhibiting different physical, chemical, and functional properties. For example, ethoxylates are low melting solids or liquids at room temperature, are completely miscible in nonpolar solvents, and their aqueous solutions have a D temperature. In comparison, alkyl polyglycosides are high-melting solids with poor solubility in non-polar solvents;
Its aqueous solution shows no cloud point. Also, compared to similar conventional non-ionic agents, furkyl polyglycosides generally produce lower surface tensions and more stable foams. Furthermore, alkyl polyglycosides are produced in different ways,
It can be manufactured using only natural raw materials. Therefore,
Compounds and compositions made from alkylpolyglycosides are expected to be biologically safer and more acceptable than conventional nonionic agents and compositions containing them. The impurities present will also be different from conventional nonionic agents. Alkyl polyglycoside is the F 1s of detergent alcohol.
It can be produced by cher glycosidation. For example, 08-C18 alcohol (ROH) + r glucose" (
G) Ten catalyst → ROG + H20 × ROGx The details of the product depend on the adjustment of the ratio of reactants. Certain products are, for example, ROGl:ROG2:RO
This will be the ratio of G3. The alkyl polyglycosides used in the present invention have a hydrophobic group containing approximately 8 to 20 carbon atoms, preferably about 10 to about 16 carbon atoms, most preferably 12 to 14 carbon atoms, and about 1 to about 3 saccharide units. , preferably 1 to 1.5, most preferably 1.2 to 1.4 on average. In the example of "Satsukarido" knit and No. 1,
Galactoside, glucoside, fructocyto or glycodyl. Mixtures of these can also be used. A preferred alkyl polyglycoside is Horizon. The average degree of polymerization of APG500 is 1.4, and APG
550 is 1,8. U.S. Patent No. 4,599,188 (
L 1enadO) further describes and characterizes alkyl polyglycosides. It is preferable that the alkyl polyglycoside is the main active ingredient, for example, preferably accounts for 30 to 60% of the active ingredient. The co-active anionic surfactants used according to the invention are of the sulfate or sulfonate type, or mixtures thereof. The sulfate can be a conventional anionic synthetic detergent or an alkanol (i.e. n=o)
Alternatively, it may be an ethoxylated alkanol sulfate hemiester. Suitable sulfates are obtained from ethoxylated or unethoxylated linear, branched, primary or secondary alcohols. Preferred alcohols are as follows. linear primary alcohols containing up to 12 moles of ethylene oxide per mole of alcohol. (ii) predominantly linear, containing 10 to 15 carbon atoms and about 25% 2-methyl branchiho, and up to 12 moles of ethylene oxide per mole of alcohol if ethoxylated; First alcohol. (iii) Random secondary alcohols containing 11 to 15 carbon atoms and 7 to 30 moles of ethylene oxide per mole of alcohol. Substantially branched primary alcohols may also be used. The cations that neutralize the anionic surfactants are preferably sodium and ammonium, the latter sulfates being able to promote the drotropes of the liquid compositions of the invention. Sulfonate is a linear alkylbenzene sulfonate,
Conventionally used sulfonates such as secondary alkyl sulfonates and alpha olefin sulfonates may be used. Amine Oxide/Betaine A third important feature of the present invention is the presence of an amine oxide or betaine as a foam enhancer. For reasons of economy and, of course, cost-effectiveness, it is preferred to avoid the use of amine oxides or betaines, particularly about 1% of the amine oxide. Preferably, the amine oxide content does not exceed 10% by weight of the active detergent mixture. Also, 41 for betaine is 30 for this mixture! It is desirable that the content does not exceed m%. The total amount of amine oxide and betaine is 12-30% by weight of the active detergent mixture. The foaming enhancer is preferably included in an amount of 2 to 6 times the total acid composition. Preferably, only betaine is used. Suitable betaines include simple betaines of the formula % and amidobetaines of the formula C3 hydroxyalkyl. An example of stafobetaine is -CO of the formula above.
The formula is obtained by replacing CO2 with the following form: -(cH2)3S03 or -CH2-Cll5II2S
o3 Suitable simple betaine is A Ibriaht &
It is Empigen BB by W 11son. This simple betaine is a CI2 in which R is obtained from coconut.
~C14I2, and has the above formula such that R6 and R1 are both methyl. Another preferred is Goldschmidt's TegOLIT, which is a complete RR6RIN-0 (wherein R is a straight or branched chain c-c18 alkyl group and each of R6 and R7 is a C1-C3 alkyl group). Suitable amine oxides are Δ1briot+t &W
ilson's Empigen OB, where R is ψ interrupted] coconut alkyl and both R6 and R7 are methyl. Compositions according to the present invention contain small amounts of other conventional ingredients such as builders, sodium chloride, sodium or ammonium chloride, corrosion inhibitors, colorants, perfumes. Conventional suds boosters such as ethanolamide may also be included. Addition of ethanolamide is optional. Addition 12-3
Make it 0x4%. A preferred ethanolamide is Ellpilan LME (Albright
& Wilson). The compositions according to the invention are used as light-duty liquid detergents, in particular for hand-washing dishes. As used herein, the term [dishes] refers to any utensil used for food preparation or food consumption. Food particles and other food residues (oils, fats,
Cleaning is required to remove proteins, starches, resins, dyes, oils, burnt organic residues from these tools. Typical compositions used for hand dishwashing include:
from about 5 to about 60% by weight, preferably about 1% by weight of the aforementioned active ingredient.
The composition contains 0 to about 40% by weight, with the remainder consisting of water and solvent. The composition according to the invention is hypoallergenic and environmentally safe;
Has good foam properties. The foaming performance and hypoallergenicity of various formulations were compared. Formulations within the scope of the invention were compared to equivalent compositions outside the scope of the invention. FOttCund 3 eiren 1951,5
An improved S chl based on the principles described in No. 3,207
Foaming performance was evaluated using the Achter-D 1erkcs test. 100 d of an aqueous solution of each test material containing 0.04% active detergent in water with a hardness of 24°H (French hardness) at a temperature of 45°C was added to a graduated chamber using a vertically vibrating perforated disc. (containing 95 parts of commercially available cooking fat, 120.25 parts of olein 1i, 25 parts of stearin@0°, and 10 parts of wheat starch in 120 parts of water) was added in an increasing amount (0,i) until the bubbles disappeared. Additions were made at 15 second intervals (10 seconds of gentle stirring and 5 seconds of stopping). Results were recorded as number of stain increments (NSI score). Score differences of 6 or more are generally considered meaningless. Each outcome typically averaged 3-4 points. Several in vitro or in vivo methods for evaluating the protein denaturing ability of surfactants and their mixtures have been reported (Miyazawa et al., I.
ntJ Cos Sci, 6.33-46.1
984 and papers cited therein). One such method is the use of small acid sfactorases obtained from the skin (263-273, 1984) or small acid sfactorases (Tanaka et al., Anal.
3 iochem, 66.489-498, 1975
) and detergents. In vivo-? f' irritation can be evaluated using the Nex wash test. In this punishment test, the undiluted product was applied to the subject's arms and legs and washed off. This treatment was repeated 4 times a day for 5 days, and the degree of erythema that appeared on the skin was evaluated by an experienced evaluator. From a comparison of the fist wheat germ phosphatase test (WGAP) results and the flex cleaning test results, the test conditions were determined. Formulations that provided enzyme inhibition of less than 50% below were shown to be substantially hypoallergenic. The Flex Wash Test showed no detectable difference in hypoallergenicity between products providing inhibition of less than 40. This test shows that enzyme tests are very sensitive;
In actual living conditions, it has become clear that below that level, any active agent or product is equally hypoallergenic, and that there is a limit level for protein degeneration. WGAP test results indicate % inhibition (i.e.
(remaining amount after subtracting % activity from 100%). Water did not provide any inhibition, ie 100% activity remained. i plate and 1 APG: Ho
r'+zon Chemicals Ne1
Both APG500 and ΔPG550° have 012 to C14 alkyl groups. The average degree of polymerization is 1.4 and 1.8t, respectively. PAS: Dobanol 23-8
(Shell). Bethaine: Empioen
OB (A 1briCIht & WilS
On). Amine oxide: Empire OB (Alb
riaht & wilson). LME: Emplilan
LME (Albriaht&W 1Ison) The variations in the amounts of the ingredients of the compositions tested are shown in the following table as a percentage of the total weight of the composition. From the foaming tests it is clear that compositions within the scope of the invention have better foaming performance than compositions outside the scope (A, B, D). Furthermore, APG500 performs better than APO550. The following M cord inhibition test was conducted. Manufacture mouth 0 enzyme j111shi11
%19/6/415 Dobanol 9l-8FO
/PAS/Betaine/LH [A19/6/415 A
PG 500/PAS/Betaine/LHE
In the 4WGAP test, APG and the non-ionic formulation showed similarly low enzyme inhibition and therefore both have similar hypoallergenic properties. Representative Patent Attorney Tsuki A Yama Takeshi

Claims (6)

【特許請求の範囲】[Claims] (1)(a)平均重合度1〜3のC_8〜C_1_8ア
ルキルポリグリコシド界面活性剤、 (b)アニオン活性剤、 (c)界面活性ベタイン及び/又はアミンオキシド、 及び任意に、 (d)エタノールアミドを含む水性液体洗剤組成物であ
つて、この組成物中、アニオン活性剤の量はベタイン及
び/又はアミンオキシドの含量の(モル基準で)1.5
倍を超えることがなく、また、ベタイン及び/又はアミ
ンオキシドと(組成物中にそれが含まれる場合は)エタ
ノールアミドとの含量が、活性成分全体の12〜30重
量%である、前記水性液体洗剤組成物。
(1) (a) a C_8-C_1_8 alkyl polyglycoside surfactant with an average degree of polymerization of 1 to 3, (b) an anionic surfactant, (c) a surfactant betaine and/or amine oxide, and optionally, (d) ethanol. An aqueous liquid detergent composition comprising an amide, in which the amount of anionic active agent is 1.5 (on a molar basis) of the content of betaine and/or amine oxide.
and the content of betaine and/or amine oxide and (if present in the composition) ethanolamide is from 12 to 30% by weight of the total active ingredients. Detergent composition.
(2)アルキルポリグリコシドが1〜1.4の平均重合
度を有する請求項1に記載の組成物。
(2) The composition according to claim 1, wherein the alkyl polyglycoside has an average degree of polymerization of 1 to 1.4.
(3)アニオン界面活性剤が第1アルキルスルフェート
である請求項1又は2に記載の組成物。
(3) The composition according to claim 1 or 2, wherein the anionic surfactant is a primary alkyl sulfate.
(4)ベタインのみを起泡増進剤として使用する請求項
1〜3のいずれかに記載の組成物。
(4) The composition according to any one of claims 1 to 3, wherein only betaine is used as a foaming enhancer.
(5)非イオン活性剤をさらに含む請求項1〜4のいず
れかに記載の組成物。
(5) The composition according to any one of claims 1 to 4, further comprising a nonionic activator.
(6)(a)1〜1.4の平均重合度を有するアルキル
ポリグリコシドを活性成分全体の50〜60重量%、(
b)第1アルキルスルフェート15〜20重量%、(c
)ベタイン10〜15重量%、 (d)エタノールアミド10〜15重量%とを含む請求
項1に記載の水性液体洗剤組成物。
(6) (a) 50 to 60% by weight of the total active ingredients of alkyl polyglycoside having an average degree of polymerization of 1 to 1.4;
b) 15-20% by weight of primary alkyl sulfates, (c
2. The aqueous liquid detergent composition of claim 1, comprising:) 10-15% by weight of betaine; and (d) 10-15% by weight of ethanolamide.
JP1113612A 1988-05-06 1989-05-02 Detergent composition Expired - Lifetime JP2664474B2 (en)

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GB888810820A GB8810820D0 (en) 1988-05-06 1988-05-06 Detergent compositions
GB8810820.4 1988-05-06

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BR (1) BR8902111A (en)
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JP2005255708A (en) * 2004-03-09 2005-09-22 Teepol Diversey Kk Condensed neutral detergent composition
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JPH0356597A (en) * 1989-07-25 1991-03-12 Kao Corp Liquid cleanser composition
JPH05140587A (en) * 1991-04-09 1993-06-08 Berol Nobel Ab Liquid dishwashing composition
KR100494626B1 (en) * 2002-04-19 2005-06-13 주식회사 엘지생활건강 Speedy rinsing dishwashing detergents compositions
JP2005255708A (en) * 2004-03-09 2005-09-22 Teepol Diversey Kk Condensed neutral detergent composition
JP2009067903A (en) * 2007-09-13 2009-04-02 Diversey Ip Internatl Bv Concentrated neutral detergent composition
JP2023013984A (en) * 2021-07-16 2023-01-26 ザ プロクター アンド ギャンブル カンパニー Liquid dish hand-wash cleaning composition
JP2023013983A (en) * 2021-07-16 2023-01-26 ザ プロクター アンド ギャンブル カンパニー Liquid dish hand-wash cleaning composition

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DE68917195T2 (en) 1994-12-01
BR8902111A (en) 1990-01-02
AU615740B2 (en) 1991-10-10
DE68917195D1 (en) 1994-09-08
ES2056215T5 (en) 2003-05-01
EP0341071B1 (en) 1994-08-03
ZA893327B (en) 1991-01-30
JP2664474B2 (en) 1997-10-15
EP0341071A2 (en) 1989-11-08
ES2056215T3 (en) 1994-10-01
AU3398989A (en) 1989-11-09
EP0341071B2 (en) 2002-11-13
EP0341071A3 (en) 1990-07-11
GB8810820D0 (en) 1988-06-08
CA1335876C (en) 1995-06-13

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