JPS63282373A - Cloth softening composition - Google Patents

Cloth softening composition

Info

Publication number
JPS63282373A
JPS63282373A JP63044066A JP4406688A JPS63282373A JP S63282373 A JPS63282373 A JP S63282373A JP 63044066 A JP63044066 A JP 63044066A JP 4406688 A JP4406688 A JP 4406688A JP S63282373 A JPS63282373 A JP S63282373A
Authority
JP
Japan
Prior art keywords
ethylene oxide
softening composition
nonionic surfactant
average
ethoxylated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP63044066A
Other languages
Japanese (ja)
Inventor
ユーニス・シーラ・ブラツクモア
ブライアン・ウイリアム・トツピング
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 JPS63282373A publication Critical patent/JPS63282373A/en
Pending legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters 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
    • 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
    • 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
    • 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
    • C11D1/86Mixtures of anionic, cationic, and 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • 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
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium 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
    • C11D1/667Neutral esters, e.g. sorbitan 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
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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
    • C11D1/74Carboxylates or sulfonates esters of polyoxyalkylene glycols
    • 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)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (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】 本発明は布地柔軟化組成物(fabric softe
ningcomposition)に関し、特に水不溶
性の陽イオン型布地柔軟剤と脂肪酸と非イオン型表面活
性剤とを含有する布地柔軟化組成物に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a fabric softening composition.
In particular, the present invention relates to fabric softening compositions containing a water-insoluble cationic fabric softener, a fatty acid, and a nonionic surfactant.

る。この問題は、凍結点以下の温度を含むような種々の
サイクル温度で貯蔵を行なう場合に顕著で礪−一カ 追り 何故なら、不可逆的なゲルが形成されうるからである。
Ru. This problem is particularly pronounced when storage is carried out at various cycling temperatures, including temperatures below the freezing point, since irreversible gels can form.

プロトン化したジ−ポリエトキシモノアルキルアミンと
低級アルコールと必要に応じ非イオン型の布地コンディ
ショニング剤とを添加して、第四アンモニウム布地柔軟
剤を含有する組成物の物理的安定性を調節することが提
案されており(ヨーロッパ特許第21476号明細′g
!i)、柔軟剤原料に存を組成物に添加しない限り物理
的安定性が得られ。
Adding a protonated di-polyethoxymonoalkylamine, a lower alcohol, and optionally a nonionic fabric conditioning agent to adjust the physical stability of the composition containing the quaternary ammonium fabric softener. has been proposed (European Patent No. 21476)
! i) Physical stability is obtained unless the softener raw material is added to the composition.

ない欠点を有する。Has no drawbacks.

今回、陽イオン型布地柔軟剤と脂肪酸とを含有する組成
物に非イオン型表面活性剤を添加すれば、ざらにアルコ
ールを添加しなくとも1回もしくは複数回の凍結/解凍
サイクルの後にも安定である組成物が得られることを知
見した。
Now, by adding a nonionic surfactant to a composition containing a cationic fabric softener and a fatty acid, it is stable after one or more freeze/thaw cycles without the need for additional alcohol. It has been found that a composition can be obtained.

したがって本発明によれば、 (i)水性ベースと、 (ii)  8ii1m%以下の水不溶性の陽イオン型
布地柔軟剤と、 (iii)少す< トモ0.2重量%の08〜C24脂
肪酸と、 (iv)非イオン型表面活性剤と、 からなり、陽イオン型布地柔軟剤と非イオン型表面活性
剤とのモル比が約40:1〜1:1の範囲テあることを
特徴とする液体布地柔軟化組成物が提供される。
According to the invention, therefore, (i) an aqueous base; (ii) not more than 1 m% of a water-insoluble cationic fabric softener; and (iii) less than 0.2 m% of a 08-C24 fatty acid. (iv) a nonionic surfactant, characterized in that the molar ratio of the cationic fabric softener to the nonionic surfactant is in the range of about 40:1 to 1:1. A liquid fabric softening composition is provided.

水不溶性の陽イオン型布地柔軟剤は、水に対する溶解度
がpH2,5カッ塩[20℃ニテ109/j1未満の任
意の布地に対し実質的に陽イオン性の化合物(fabr
ic−substantive cationic c
ompound)とすることができる。極めて好適な物
質は2本の゛C12〜G24アルキルもしくはアルケニ
ル基を有する第四アンモニウム塩であり、前記鎖は必要
lc応L;たとえば−OH,−0+、−CONH−。
A water-insoluble cationic fabric softener is a substantially cationic compound (fabr.
ic-substantive cationic c
compound). Highly preferred substances are quaternary ammonium salts having two C12-G24 alkyl or alkenyl groups, said chains having the necessary lc properties; for example -OH, -0+, -CONH-.

−COO−などの官能基により適宜置換または中断され
ていてもよい。
It may be appropriately substituted or interrupted by a functional group such as -COO-.

公知の実質的に水不溶性の第四アンモニウム化〔式中、
RおよびR2は約12〜24個の炭素原子を有する炭化
水素基を示し、R3お、よびR4は約1〜4個の炭素原
子を有する炭化水素基を示し、Xは陰イオンであって、
好ましくはハロゲンイオン、メチルサルフェートおよび
エチルサルフェート基から選択される〕 を有する。
Known substantially water-insoluble quaternary ammonizations [wherein
R and R2 represent a hydrocarbon group having about 12 to 24 carbon atoms, R3 and R4 represent a hydrocarbon group having about 1 to 4 carbon atoms, and X is an anion;
preferably selected from halogen ions, methyl sulfate and ethyl sulfate groups.

これら第四柔軟剤の代表例には、シタロージメチルアン
モニウムクロライドニジタロージメチルアンモニウムメ
チルサルフェート;ジヘキ号デシルジメチルアンモニー
クムクUライド;ジ(水素化タローアルキル)ジメチル
アンモニウムクロライド:ジオクタデシルジメチルアン
モニウムクロライド;ジエイコシルジメチルアンモニウ
ムクロライド:ジドコシルジメヂルアンモニウムクロラ
イド:ジ(水素化タロー)ジメチルアンモニウムメチル
サルフェート;ジヘキサデシルジエチルアンモニウムク
ロライド;ジ(ココナツアルキル)ジメチルアンモニウ
ムクロライドが包含される。さらに、軟質もしくは硬質
脂肪酸をベースとするジアルキルエトキシルメチルアン
モニウムサルフェートも適当である。シタロージメチル
アンモニウムクロライド、ジ(水素化タローアルキル)
ジメチルアンモニウムクロライド、ジ(ココナツアル4
−ル)ジメチルアンモニウムクロライドおよびジ(ココ
ナツアルキル)ジメチルアンモニウムメしサルフェート
も好適である。
Typical examples of these fourth softeners include citallow dimethyl ammonium chloride nitallow dimethyl ammonium methyl sulfate; dihexyl dimethyl ammonium chloride; di(hydrogenated tallow alkyl) dimethyl ammonium chloride; dioctadecyl dimethyl ammonium chloride; Dieicosyldimethylammonium chloride: didocosyldimethylammonium chloride: di(hydrogenated tallow)dimethylammonium methyl sulfate; dihexadecyldiethylammonium chloride; di(coconut alkyl)dimethylammonium chloride. Furthermore, dialkylethoxylmethylammonium sulfates based on soft or hard fatty acids are also suitable. Citalo dimethyl ammonium chloride, di(hydrogenated tallow alkyl)
Dimethylammonium chloride, di(coconut al 4)
-l)dimethylammonium chloride and di(coconut alkyl)dimethylammonium sulfate are also suitable.

他の好適な水不溶性の陽イオン型物質は式:〔式中、R
6は1〜4個、好ましくは1個もしくは2個の炭素原子
を有するアルキルもしくはヒドロキシアル4−ル基であ
り、R7は8−.25個の炭素原子を有するアルキルも
しくはアルケニル基であり、R8は8〜25Imの炭素
原子を有するアルキルもしくはアルケニル基であり、R
9は水素または1〜4個の炭素原子を有するアルキルで
あり、かつ八′″は陰イオン、好ましくはハロゲンイオ
ン、メトサルフェートもしくはエトサルフェートである
) を有すると考えられるアルキルイミダゾリニウム塩であ
る。好適なイミダゾリニウム塩には、1−メチル−1−
(タローイルアミド)エチル−2−タローイル−4,5
−ジヒドロイミダゾリニウムメトサルフェートおよび1
−メチル−1−(バルミトイルアミド)エチル−2−オ
クタデシル−4,5−ジヒドロ−イミダゾリニウムクロ
ライドが包含される。他の有用なイミダゾリニウム塩は
、2−へブタデシル−1−メチル−1−(2−ステアリ
ルアミド)−エチル−イミダゾリニウムクロライドおよ
び2−ラウリル−1−ヒドロキシエチル−1−オレイル
−イミダゾリニウムクロライドである。さらに、米国特
許第4127489号も適当である。各種の陽イオン型
布地柔軟剤の混合物も使用することができる。
Other suitable water-insoluble cationic substances have the formula:
6 is an alkyl or hydroxyal 4-yl group having 1 to 4, preferably 1 or 2 carbon atoms, R7 is 8-. an alkyl or alkenyl group having 25 carbon atoms, R8 is an alkyl or alkenyl group having 8 to 25 Im carbon atoms, and R
9 is hydrogen or alkyl having 1 to 4 carbon atoms, and 8' is an anion, preferably a halogen ion, methosulfate or ethosulfate). Suitable imidazolinium salts include 1-methyl-1-
(Tallowylamide)ethyl-2-tallowyl-4,5
- dihydroimidazolinium methosulfate and 1
-Methyl-1-(balmitoylamido)ethyl-2-octadecyl-4,5-dihydro-imidazolinium chloride. Other useful imidazolinium salts are 2-hebutadecyl-1-methyl-1-(2-stearylamido)-ethyl-imidazolinium chloride and 2-lauryl-1-hydroxyethyl-1-oleyl-imidazolinium chloride. It is nium chloride. Additionally, US Pat. No. 4,127,489 is also suitable. Mixtures of various cationic fabric softeners can also be used.

組成物中の陽イオン型布地柔軟剤の量は、好ましくは1
mω%以上、特に好ましくは3〜6重都%である。
The amount of cationic fabric softener in the composition is preferably 1
It is mω% or more, particularly preferably 3 to 6 mω%.

本発明に使用することができる適当な脂肪酸は、c  
”C24アルキルもしくはアルケニルの線状もしくは分
枝鎖のモノカルボン酸またはその重合体である。好まし
くは飽和脂肪酸が使用され、特に硬化タローC16〜C
18脂肪酸が使用される。各種脂肪酸の混合物も使用す
ることができる。
Suitable fatty acids that can be used in the present invention include c
"C24 alkyl or alkenyl linear or branched monocarboxylic acids or polymers thereof. Preferably saturated fatty acids are used, especially hardened tallow C16-C
18 fatty acids are used. Mixtures of various fatty acids can also be used.

組成物中の脂肪酸の量は好ましくは8型組%未満、特に
好ましくは0,2〜2゜51憬%である。
The amount of fatty acids in the composition is preferably less than 8%, particularly preferably between 0.2 and 2.51%.

陽イオン型布地柔軟剤と脂肪酸とのモル比は少なくとも
1:1、好ましくは4:1〜9:1の範囲である。
The molar ratio of cationic fabric softener to fatty acid is at least 1:1 and preferably ranges from 4:1 to 9:1.

使用しうる適当な非イオン型表面活性剤は特に、疎水性
基と反応性水素原子とを有する化合物、たとえば脂肪族
アルコール、酸もしくはアルキルフェノールとアルキレ
ンオキシド(特にエチレンオキシドもしくはエチレンオ
キシドとプロピレンオニをシトとの組合せ)との反応生
成物を包含する。
Suitable nonionic surfactants that can be used are, in particular, compounds having hydrophobic groups and reactive hydrogen atoms, such as aliphatic alcohols, acids or alkylphenols and alkylene oxides (in particular ethylene oxide or ethylene oxide and propylene oxide). combination).

非イオン型表面活性剤としては、通常最高25EO(す
なわち1分子当り最高25単位のエチレンオキシドを含
む)のアルキル(06〜C22)フェノール−エチレン
オキシド縮合物、通゛常最高40EOまでのエチレンオ
キシド脂肪族(C−C22)第一もしくは第二の線状も
しくは分枝鎖アルコールとの縮合物、並びにエチレンオ
キシドをプロピレンオキシドとエチレンジアミンとの反
応生成物と縮合させて得られた生成物である。その他の
いわゆる非イオン型表面活性剤にはアミンオキシド、ア
ルキルポリグリコシド、エトキシル化ヒマシ油およびソ
ルビタンエステルが包含される。
Nonionic surfactants typically include alkyl (06-C22) phenol-ethylene oxide condensates of up to 25 EO (i.e. containing up to 25 units of ethylene oxide per molecule), ethylene oxide aliphatic (C -C22) condensates with first or second linear or branched alcohols, as well as products obtained by condensing ethylene oxide with the reaction product of propylene oxide and ethylenediamine. Other so-called nonionic surfactants include amine oxides, alkyl polyglycosides, ethoxylated castor oil and sorbitan esters.

非イオン型表面活性剤の好ましい、量は0.1〜4.5
重量%の範囲、特に0.15〜3重量%の範囲である。
The preferred amount of nonionic surfactant is 0.1 to 4.5
% by weight, especially in the range from 0.15 to 3% by weight.

陽イオン型布地柔軟剤と非イオン型表面活性剤とのモル
比は約40:1〜1:1、好ましくは約18:1〜3:
1の範囲である。
The molar ratio of cationic fabric softener to nonionic surfactant is about 40:1 to 1:1, preferably about 18:1 to 3:
The range is 1.

組成物にさらに、C−C4アルカノールおよび多価アル
コール(これらの物質を添加しなくても本発明の利点は
得られる)のような非水性溶剤、pH緩衝剤たとえば燐
酸、安息香酸もしくはクエン酸のような弱R(組成物の
pHは好ましくは6.0未満である)、再湿潤剤、粘度
改良剤たとえば約20〜6000ppmの°量で含ませ
る電解質およびC−C24脂肪酸、ゲル化防止剤、香料
、香料キャリヤ、蛍光剤、着色料、ハイドロトロープ剤
、消泡剤、再付着防止剤、酵素、艶出剤(\optic
albriQhteniQ a!]entS) 、乳白
化剤、安定剤たとえばグアガムおよびポリエチレングリ
コール、収縮防止剤、皺防止剤、繊維捲縮剤、斑点防止
剤、汚れ放出剤、殺菌剤、殺黴剤、酸化防止剤、腐食防
止剤、・保存料たとえばBronol)Of (登録商
標)、2−プロモー2−二トロプロパン−1,3−ジオ
ールの市販品、染料、漂白剤および漂白先駆体、ドレー
プ付与剤、静電防止剤並びにアイロン助剤たとえばシリ
コーンなどから選択される1種もしくはそれ以上の任意
成分を含有させることもできる。
The composition may further contain non-aqueous solvents such as C-C4 alkanols and polyhydric alcohols (the benefits of the invention are obtained without the addition of these substances), pH buffering agents such as phosphoric acid, benzoic acid or citric acid. weak R (the pH of the composition is preferably less than 6.0), rewetting agents, viscosity modifiers such as electrolytes and C-C24 fatty acids included in amounts of about 20 to 6000 ppm, antigelling agents, Fragrances, fragrance carriers, fluorescent agents, colorants, hydrotropes, antifoaming agents, anti-redeposition agents, enzymes, polishing agents (\optic
albriQhteniQ a! ]entS), opacifiers, stabilizers such as guar gum and polyethylene glycols, anti-shrink agents, anti-wrinkle agents, fiber crimping agents, anti-spot agents, stain release agents, bactericidal agents, fungicides, antioxidants, anti-corrosion agents. agents, preservatives such as Bronol® Of®, commercial products of 2-promo-2-nitropropane-1,3-diol, dyes, bleaching agents and bleaching precursors, draping agents, antistatic agents and One or more optional ingredients selected from ironing aids such as silicones may also be included.

これらの任意成分を、添加する場合には、それぞれ組成
物の5重量%までの量とする。
These optional ingredients, if added, each amount to up to 5% by weight of the composition.

本発明組成物に使用するのに適したシリコーン類は、ア
ルキル基が1〜5個の炭素原子を有する主として線状の
ポリジアルキルもしくはアルキルアリールシロキサンで
ある。これらシロキサンがアミドもしくはアミノ置換さ
れていてもよい。シロキサンがアミン置換されている場
合、アミノ基を四級化することができる。
Silicones suitable for use in the compositions of the invention are primarily linear polydialkyl or alkylarylsiloxanes in which the alkyl group has 1 to 5 carbon atoms. These siloxanes may be amide or amino substituted. If the siloxane is amine-substituted, the amino groups can be quaternized.

組成物に、陽イオン型布地柔軟剤の他に、他の非陽イオ
ン型柔軟剤たとえば非イオン型布地柔軟剤を含有させる
こともできる。適当な非イオン型布地柔軟剤にはラノリ
ンおよびその誘導体が包含容も参照により本明細書に包
合されるものとする。
In addition to cationic fabric softeners, the compositions can also contain other non-cationic fabric softeners, such as nonionic fabric softeners. Suitable nonionic fabric softeners include lanolin and its derivatives, which are also incorporated herein by reference.

典型的には、前記物質は組成物に対し0.5〜10重6
%の範囲の量で含ませる。
Typically, the material will weigh between 0.5 and 10% by weight of the composition.
Contain in an amount in the range of %.

使用に際し、本発明の布地コンディショニング組成物を
多量の水に添加して液体を形成することができ、この液
体を処理すべき布地と接触させる。
In use, the fabric conditioning composition of the present invention can be added to a quantity of water to form a liquid, which is contacted with the fabric to be treated.

一般に、この液体中の陽イオン型布地柔軟剤、脂肪酸お
よび非イオン型表面活性剤の全濃度は約30ppm〜5
001)+11の範囲である。布地対液体の重量比は好
ましくは約25:1未満、特に好ましくは約10:1〜
約4:1の範囲である。
Generally, the total concentration of cationic fabric softeners, fatty acids, and nonionic surfactants in this liquid is about 30 ppm to 5
001)+11. The weight ratio of fabric to liquid is preferably less than about 25:1, particularly preferably from about 10:1
The ratio is approximately 4:1.

本発明の組成物は各種の方法で作成することができる。Compositions of the invention can be made in a variety of ways.

1つの適する方法では、陽イオン型布地柔軟剤と脂肪酸
との溶融混合物を形成し、この溶融混合物を攪拌しなが
ら水に添加して分散物を形成し、次いで非イオン型表面
活性剤と任意成分とを添加する。他の適する方法では、
非イオン型表面活性剤を分散物が形成される前の溶融混
合物に添加する。
One suitable method involves forming a molten mixture of the cationic fabric softener and the fatty acid, adding this molten mixture to water with agitation to form a dispersion, and then adding the nonionic surfactant and optional ingredients. and add. In other suitable ways,
A nonionic surfactant is added to the molten mixture before the dispersion is formed.

以下、非限定実施例により本発明をさらに説明する。実
施例において、重量は全て活性物質の重量%として表わ
す。
The invention will now be further illustrated by non-limiting examples. In the examples, all weights are expressed as % by weight of active substance.

実施例1 液体の布地柔軟化組成物を次のように作成した。Example 1 A liquid fabric softening composition was made as follows.

陽イオン型布地柔軟剤と脂肪酸とを予備混合し、透明と
なるまで加熱した(60〜75℃)。このように形成さ
れた溶融混合物を少なくとも1分間かけて浸漬パイプを
介して45〜&O℃の水に゛絶えず攪拌、しながら添加
して分散物を形成させた。香料を含む他の少量成分を絶
えず攪拌しながら添加すると共に、分散物の温度を35
℃以上にした。特に好まゑ しくは、混合物渋35℃もしくはそれ以下まで冷却した
後に非イオン型表面活性剤を添加した。
The cationic fabric softener and fatty acid were premixed and heated until clear (60-75°C). The molten mixture thus formed was added via a dip pipe to water at 45-0.degree. C. with constant stirring over a period of at least 1 minute to form a dispersion. Other minor ingredients, including perfume, are added with constant stirring and the temperature of the dispersion is increased to 35°C.
The temperature was above ℃. Particularly preferably, the nonionic surfactant is added after the mixture has cooled to 35°C or below.

この実施例において、使用した成分の量は、最終生成物
が重量%とじて表わして次の組成を有するような呈とし
た。
In this example, the amounts of ingredients used were such that the final product had the following composition, expressed as weight percent.

アルクワット2H73,6% ブリスチレン 4916      0.6%ノニデッ
ト LE 6T      O,25%香    料 
                   0.13 %
陽イオン型′・非イオン型の 大凡のモル比        11.1比較の目的で、
組成物からノニデットLE6Tを除いた以外は*施例1
と同一の組成物を作成した(例IA)。
Alquat 2H73, 6% Brystyrene 4916 0.6% Nonidet LE 6T O, 25% Fragrance
0.13%
Approximate molar ratio of cationic form and nonionic form 11.1 For comparison purposes,
*Example 1 except that Nonidet LE6T was removed from the composition
(Example IA).

両製品に1回、3回および6回の凍結/解凍サイクルを
課して肉眼評価した。
Both products were subjected to 1, 3 and 6 freeze/thaw cycles for visual evaluation.

この試験における凍結/解凍サイクルには、1009の
製品をネジキャップ付きのポリエチレン壜に一12℃も
しくはそれ以下の温度で16時間貯蔵する工程を含めた
。前記した温度は、製品を完全に凍結させうる温度であ
る。次いで、この製品を室温にて8時間解凍させた。
The freeze/thaw cycle in this study included storing the 1009 product in a polyethylene bottle with a screw cap for 16 hours at a temperature of -12°C or below. The above-mentioned temperature is a temperature at which the product can be completely frozen. The product was then allowed to thaw at room temperature for 8 hours.

1回の凍結/解凍サイクルの後、実施例1の組成物は通
常よりも僅かに濃厚となった。3回および6回の凍結/
解凍サイクルの後も、実施例1の組成物は通常の濯ぎコ
ンディショナーのis性を有しており、連続流(C0n
tinLIOu3 Stream)として注ぐことがで
きた。1回、3回および6回の凍結/解凍サイクルの後
のN 1Aの組成物は、僅かな流動性を有しているが連
続流として注ぎ得ないものであった。
After one freeze/thaw cycle, the composition of Example 1 became slightly thicker than normal. 3 and 6 freezes/
Even after the thaw cycle, the composition of Example 1 has the properties of a conventional rinse conditioner, with continuous flow (C0n
It was possible to pour it as tinLIOu3 Stream). The N 1A composition after 1, 3 and 6 freeze/thaw cycles had slight flowability but could not be poured as a continuous stream.

これらの結果から明らかなように、陽イオン型布地柔軟
剤と脂肪酸とを含有する組成物に少量の非イオン型表面
活性剤を添加すれば、優れた外観と6回の凍結/解凍サ
イクルの後にも維持される流動特性とを有する製品が得
られる。
These results demonstrate that the addition of a small amount of non-ionic surfactant to a composition containing a cationic fabric softener and a fatty acid provides excellent appearance and after 6 freeze/thaw cycles. A product is obtained which has flow properties that are also maintained.

実施例2 この実施例では、ノニデットLE6Tを他の非イオン型
表面活性剤で置換した。型組%として表わして次の組成
を有する組成物を前記の方法により作成した。
Example 2 In this example, Nonidet LE6T was replaced with another nonionic surfactant. A composition having the following composition, expressed as mold %, was prepared by the method described above.

アルクワット2HT        3.6%ブリスチ
レン 4916      0.6%非イオン型表面活
性剤     0.4%香   料         
          0.13 %比較の目的で、非イ
オン型表面活性剤を含有しない組成物(例2L)を作成
し、試験した。例2Aにおいては0.4%でなり0.2
%の槽のAPG300を使用した。各組成物を1回およ
び3回の凍結/解凍サイクルの後に次のキャップ:ディ
スペンサ試験にかけた。
Alquat 2HT 3.6% Brystyrene 4916 0.6% nonionic surfactant 0.4% fragrance
0.13% A composition containing no nonionic surfactant (Example 2L) was prepared and tested for comparison purposes. In Example 2A, it is 0.4% and 0.2
% tank of APG300 was used. Each composition was subjected to the following cap:dispenser test after one and three freeze/thaw cycles.

製品を解凍させた後、既知ω(一般に20g)を全容積
約2513かつ厖知重量を有する内ネジ付きのキャップ
に秤量して入れた。次いで、このキャップを廃棄容器の
上に10秒間倒置させて、再秤禮した。結果をキャップ
中に秤量して入れた製品の量に対する%として表わした
。凍結前に、これらの試料はギャップ内に約10%残留
することが判明した。
After thawing the product, a known amount (typically 20 g) was weighed into an internally threaded cap having a total volume of approximately 2513 and a known weight. The cap was then inverted over the waste container for 10 seconds and reweighed. The results were expressed as a percentage of the amount of product weighed into the cap. Prior to freezing, these samples were found to remain approximately 10% within the gap.

結果は次の通りである。The results are as follows.

得られた結果から明らかなように、ノニゲットしE 6
Tの代りに各種の他の非イオン型表面活性剤の1種を使
用しても陽イオン型布地柔軟剤と脂肪酸とを含有する組
成物に少量の非イオン型表面活性剤を添加して得られる
効果が保持される。幾種の非イオン型表面活性剤では、
数回の凍結/解凍サイクルの後に最適な効果が得られた
As is clear from the results obtained, Noniget and E6
Substituting one of a variety of other nonionic surfactants for T may also result in the addition of small amounts of nonionic surfactants to compositions containing cationic fabric softeners and fatty acids. effect is retained. For some nonionic surfactants,
Optimal effect was obtained after several freeze/thaw cycles.

さらに、ノニデットLE6Tの代りにツイーン20、ア
ルフォール 1214−7、アルフォール1214−1
1、アルフォール1214−13、ブリッジ 30、ブ
リッジ 35、ルチンソールAO7、ルチンソールこの
実施例では、重量比で6:1のアルクワット2HT:ブ
リスチレン 4916を含む活性成分4.2%および香
料0.13%を有する組成物の凍結/解凍安定性に対す
る非イオン型表面活性剤の爾の影響を調べた。これらの
組成物は、上記の方法で作成した。非イオン型表面活性
剤の口は、最終組成物の重量%として表わした。これら
の製品を、上記のキャップ・ディスペンサ試験により 
1回の凍結/解凍サイクルの侵に評価した。
Furthermore, instead of Nonidet LE6T, Tween 20, Alfor 1214-7, Alfor 1214-1
1, Alfor 1214-13, Bridge 30, Bridge 35, Lutinsol AO7, Lutinsol This example contains 4.2% active ingredient and 0.13% fragrance, including a 6:1 weight ratio of Alquat 2HT:Brystyrene 4916 The effect of nonionic surfactants on the freeze/thaw stability of compositions with These compositions were made as described above. The amount of nonionic surfactant was expressed as weight percent of the final composition. These products were tested using the cap/dispenser test described above.
The damage was evaluated after one freeze/thaw cycle.

ffiwAイオン型: 実施例   1rイオン型   重量% 残留% J1
イオン望の1−一五」」口(皿−一 −大凡のモル比3
A   :n−カス35   0.4    80  
 39:1[31,04716:I G               2.0    62
   8:ID               4.0
    16   4:IE            
   6.0    13   3:IF      
         8.0    11   2:IG
   APG    300   0.2    69
   13:IH05575:I I               CO403:IJ 
              2.0    22  
 1:IK               3.0  
  17    +:IL             
  4.OSep    1:IM  ドハ/−)Lt
  45−18  0.4    85   16: 
 IN               1.0    
31   7:70              2.
0    15   3:IP           
    4.0    13   2:IQ     
          6.0    Sep    1
:1川     陽イオン型: 実施例   非イオン型   重量% 残留% 非イオ
ン型の一狡−*A(D工±且 Rゲナボール 0−200  0.4    59  
 18:  IS              1.0
    21   7:IT            
  2.0    12   4:IU       
       4.0    9   2:IV   
           8.OSep    1:IW
   /ニア’ット LE 6T  O,110027
:  TX              O,2553
11:IY              O,4367
:IZ              O,6335:I
AA             0.8    19 
  3:1B8            1.0   
 Sep    3:1表中5ep=相分離 これらの結果から明らかなように、多量の非イオン型表
面活性剤(陽イオン型:非イオン型のモル比は小さい)
は凍結/解凍サイクルに対しかなり不安定にさせる。
ffiwA ion type: Example 1r ion type Weight% Residual % J1
Ion desired 1-15'' mouth (dish-1 - approximate molar ratio 3
A: n-cass 35 0.4 80
39:1 [31,04716:I G 2.0 62
8: ID 4.0
16 4:IE
6.0 13 3:IF
8.0 11 2:IG
APG 300 0.2 69
13:IH05575:I I CO403:IJ
2.0 22
1:IK 3.0
17+:IL
4. OSep 1:IM Doha/-)Lt
45-18 0.4 85 16:
IN 1.0
31 7:70 2.
0 15 3:IP
4.0 13 2:IQ
6.0 Sep 1
:1 River Cation type: Example Non-ion type Weight % Residual % Non-ion type Ichigo-*A (D engineering ± and R Genabol 0-200 0.4 59
18: IS 1.0
21 7: IT
2.0 12 4:IU
4.0 9 2:IV
8. OSep 1:IW
/ Near't LE 6T O, 110027
: TX O, 2553
11:IYO,4367
:IZO,6335:I
AA 0.8 19
3:1B8 1.0
Sep 3:1 5ep in the table = phase separation As is clear from these results, a large amount of nonionic surfactant (the molar ratio of cationic type to nonionic type is small)
makes it quite unstable to freeze/thaw cycles.

111」 この実施例では、4.2%の活性成分と陽イオン型布地
柔軟剤対脂肪酸の重量比6:1とを有するもの以外の組
成物に対する紙積のノニデットL[6Tの作用を調べた
。これらの組成物は上記と同様に作成し、成分%は最終
製品におけるその重量%を意味する。
111'' In this example, the effect of paper weight Nonidet L[6T was investigated on compositions other than those having 4.2% active ingredient and a 6:1 weight ratio of cationic fabric softener to fatty acid. . These compositions were made as described above, and % of an ingredient refers to its weight % in the final product.

・−例NQ       ABCD 成分% DMDI−ITAc   3.2 3.2 4.8 4
.8HTFA、                 0
.3    0.3     1.2     1.2
香    Fl       6T  O,120,1
20,330,33ノニデツトLE  6丁0.2  
− 0.4  −陽イオン型:非イオン型の人民のモル
比刊キ命ツ;=ネ               lλ
;I          タ::これらの組成物を上記
のキャップ:ディスベンザ試験により評価した。
・-Example NQ ABCD Component % DMDI-ITAc 3.2 3.2 4.8 4
.. 8HTFA, 0
.. 3 0.3 1.2 1.2
Incense Fl 6T O,120,1
20,330,33 Nonidetsu LE 6-piece 0.2
- 0.4 - Cation type: Non-ion type people's molar ratio; = ne lλ
;Ita::These compositions were evaluated by the cap:disbenza test described above.

実施個順      % A38 B          ゲル C25 [)           80 何れの場合にも、非イオン型表面活性剤の添加により製
品の外観および流動特性が向上することが判明した。
In order of implementation: % A38 B Gel C25 [) 80 In each case, it was found that the addition of a nonionic surfactant improved the appearance and flow characteristics of the product.

実施例5 次の組成を有する組成物を上記と同様に作成した。ここ
でも、各成分の社は最終製品の組成物におけるm1%を
意味する。
Example 5 A composition having the following composition was prepared in the same manner as above. Again, the value of each component refers to ml% of the composition of the final product.

工                        
 ゞ”    Ill    l    I+  00
                    ″ ゞ” 
   Ill    l    l−−QQ LL                       
      FJ”’    l  :  、l、I 
   I  I  l  0LLI         
               C’J(’J1 1 
   ゛    1 100 o                        
  c′J+/)−1 11ift     l ○                      υ 
〜−1J) 1     +111”’−”  0 a:lc″ ”   ”1111”−11≦ (F’)C′1 ”   ”+111   1 これらの組成物について、1回の凍結/解凍ナイクル後
肉眼評価した。何れの場合にも、非イオン型表面活性剤
の添加により、組成物の外観および流動特性が向上した
。この実施例は、非イオン型表面活性剤を添加する有利
な効果がアルクワット2HTおよびプリスチレン491
6を含有する組成物のみに限らないことを示している。
engineering
ゞ” Ill l I+ 00
″ ゞ”
Ill l l--QQ LL
FJ"' l: , l, I
I I l 0LLI
C'J('J1 1
゛ 1 100 o
c'J+/)-1 11ift l ○ υ
~-1J) 1 +111"'-"0 a:lc"""1111"-11≦(F')C'1""+111 1 These compositions were visually evaluated after one freeze/thaw cycle. . In both cases, the addition of nonionic surfactants improved the appearance and flow properties of the compositions. This example shows that the beneficial effect of adding nonionic surfactants to ALCUAQAT 2HT and PRISTYRENE 491
This shows that the composition is not limited to only those containing 6.

実施例に の実施例においては、次の組成物の柔軟性能を調べた。Example In the Examples, the flexibility capabilities of the following compositions were investigated.

1ma漫           6A    6B”成
  分  % アルクワット        3.6  3.6プリス
テレン4916     0.6  0.6ドバノール
14−18      0.21   −香    料
                0.13   0.
13アルクワット2HT:    30.1   −ド
パノール14〜18のモル比 末比 較 例 専門家パネルの主観的評価により、1回の凍結/解凍サ
イクルの後に柔軟性能を評価した。
1 maman 6A 6B" Ingredients % Alquat 3.6 3.6 Pristerene 4916 0.6 0.6 Dovanol 14-18 0.21 -Fragrance 0.13 0.
13 Alquat 2HT: 30.1-Dopanol 14-18 Molar Ratio Comparison Example Flexibility capacity was evaluated after one freeze/thaw cycle by subjective evaluation of an expert panel.

組成物を水道水に分散させて、0.01%の活性成分を
含有する希釈水性分散液を得た。4枚の木綿タオル(5
09)を、ターゴトメータにてljlの水性分散液を用
いて室温で5分間濯いだ。
The composition was dispersed in tap water to obtain a dilute aqueous dispersion containing 0.01% active ingredient. 4 cotton towels (5
09) was rinsed with an aqueous dispersion of ljl in a tergotometer for 5 minutes at room temperature.

次いで、布地を遠心乾燥させかつ1晩ライン乾燥した。The fabric was then spin dried and line dried overnight.

これらの組成物は同様な柔軟作用を示すことが判明した
。しかしながら、1回の凍結/jlN凍サイクサイクル
非イオン型表面活性剤を含有しない組成物(例6B)は
僅かに流動性であるが連続流として注ぎ得ないのに対し
、本発明による組成物は通常の濯ぎコンディショナーの
流動性よりも僅かに濃厚であったが連続流として注ぐこ
とができた。
These compositions were found to exhibit similar softening effects. However, one freeze/jlN cryocycle composition containing no nonionic surfactant (Example 6B) is slightly flowable but cannot be poured as a continuous stream, whereas the composition according to the invention It was slightly thicker than the flowability of a normal rinse conditioner, but could be poured as a continuous stream.

1分子当り平均7個のエチレンオキシド基でエトキシル
化されたC1□〜C14直鎖アルコール(偶母==AP
G300: 09〜C11アルコールをベースとしかつアルコール1
モル当り平均1.6個のグリコシド環を有するアルキル
ポリグリコシド(51%活性溶液として供給される)。
C1□~C14 straight chain alcohol ethoxylated with an average of 7 ethylene oxide groups per molecule (even mother==AP
G300: Based on 09-C11 alcohol and alcohol 1
Alkyl polyglycoside with an average of 1.6 glycoside rings per mole (supplied as a 51% active solution).

市販の二硬化タロージメチルアンモニウムクロライド(
D M D HT A C)  (75%活性ペースト
と1分子当り平均4個のエチレンオキシド基でエトキシ
ル化されたCI2〜C14直鎖アルコール(偶ブリジ3
0と同様であるが、ただし1分子当り平均23個のエチ
レンオキシド基を有する。
Commercially available di-cured tallow dimethylammonium chloride (
D M D HT A C) (75% active paste and CI2-C14 linear alcohol ethoxylated with an average of 4 ethylene oxide groups per molecule (even bridge 3
0, but with an average of 23 ethylene oxide groups per molecule.

DMCAO: 30%溶液として供給されるジメチルココアミンオキシ
ド。
DMCAO: Dimethylcocoamine oxide supplied as a 30% solution.

爆速W 1)91〜6: 1分子当り平均6個のエチレンオキシド基でエトキシル
化されたC −5−C11分岐鎖の−級アルコ1分子当
り平均18個のエチレンオキシド基で工1分子当り平均
35@のエチレンオキシド基で工1分子当り平均50個
のエチレンオキシド基で工1分子当り平均200個のエ
チレンオキシド基で1分子当り平均7個のエチレンオキ
シド基でエルテンソールOA 7と同様であるが、ただ
し1ドパノール91〜6と同様な物質であるが、ただし
揮発性物質を除去するためトッピングされている。
Explosive speed W 1) 91 to 6: C-5-C11 branched -class alkyl ethoxylated with an average of 6 ethylene oxide groups per molecule. An average of 35 per molecule with an average of 18 ethylene oxide groups per molecule. With an average of 50 ethylene oxide groups per molecule, an average of 200 ethylene oxide groups per molecule, and an average of 7 ethylene oxide groups per molecule. Same as Eltensol OA 7, but 1 dopanol 91 - Similar material to 6, but topped to remove volatiles.

ノニルフェノール20EO: 1分子当り20個のエチレンオキシド基でエトキシル化
されたノニルフェノール。
Nonylphenol 20EO: Nonylphenol ethoxylated with 20 ethylene oxide groups per molecule.

プリステ吃5端詰闇e 軟質脂肪酸をベースとするジアルキルエトキシ、アンモ
ニウムメトサルフェート。
Dialkyl ethoxy, ammonium methosulfate based on soft fatty acids.

1分子当り平均11個のエチレンオキシド基で工1分子
当り平均7個のエチレンオキシド基で工1分子当り20
個のエチレンオキシド基を有する娼共凸 (Mar+5oft)222  : 軟質タローをベースとするジアミド四級物。
With an average of 11 ethylene oxide groups per molecule, an average of 7 ethylene oxide groups per molecule with an average of 20 ethylene oxide groups per molecule.
Coconvex (Mar+5oft) 222 having ethylene oxide groups: Diamide quaternary product based on soft tallow.

ffi所東人ユニ’J−バー・ナームロービ拳ベンノー
トシャープ
ffi Tojin Uni' J-Bar Naamrobi Fist Ben Note Sharp

Claims (7)

【特許請求の範囲】[Claims] (1) (i)水性ベースと、 (ii)8重量%以下の水不溶性の陽イオン型布地柔軟
剤と、 (iii)少なくとも0.2重量%のC_8〜C_2_
4脂肪酸と、 (iv)非イオン型表面活性剤と、 からなり、陽イオン型布地柔軟剤と非イオン型表面活性
剤とのモル比が約40:1〜1:1の範囲であることを
特徴とする液体布地柔軟化組成物。
(1) (i) an aqueous base; (ii) not more than 8% by weight of a water-insoluble cationic fabric softener; and (iii) at least 0.2% by weight of C_8-C_2_
(iv) a nonionic surfactant, and the molar ratio of the cationic fabric softener to the nonionic surfactant is in the range of about 40:1 to 1:1. A liquid fabric softening composition characterized by:
(2)非イオン型表面活性剤が、 (i)脂肪族アルコールとアルキルフェノールとのアル
キレンオキシド付加物、 (ii)アミンオキシド、 (iii)アルキルポリグリコシド、 (iv)エトキシル化ヒマシ油、 (v)ソルビタンエステルおよびそのエトキシル化誘導
体、並びに (vi)前記物質の混合物、 よりなる群から選択される請求項1記載の液体布地柔軟
化組成物。
(2) The nonionic surfactant is (i) an alkylene oxide adduct of an aliphatic alcohol and an alkylphenol, (ii) an amine oxide, (iii) an alkyl polyglycoside, (iv) an ethoxylated castor oil, (v) The liquid fabric softening composition of claim 1 selected from the group consisting of sorbitan esters and ethoxylated derivatives thereof, and (vi) mixtures of said substances.
(3)非イオン型表面活性剤が、 (i)ジメチルココアミンオキシド、 (ii)1分子当り平均20個のエチレンオキシド基で
エトキシル化されたノニルフェノール、(iii)1分
子当り平均20個のエチレンオキシド基でエトキシル化
されたポリオキシエチレンソルビタンモノラウレート、 (iv)1分子当り平均20個のエチレンオキシド基で
エトキシル化されたポリエチレンソルビタンモノラウレ
ートとソルビタンモノラウレートとの重量比50/50
の重量比における混合物、(v)9〜11個の炭素原子
を有しかつ1分子当り平均6個のエチレンオキシド基で
エトキシル化された分枝鎖の一級アルコール、 (vi)12〜14個の炭素原子を有しかつ1分子当り
平均4、7、11、13もしくは23個のエチレンオキ
シド基でエトキシル化された直鎖の一級アルコール、お
よび (vii)13〜15個の炭素原子を有しかつ1分子当
り平均7、8もしくは11個のエチレンオキシド基でエ
トキシル化された分枝鎖の一級アルコール、よりなる群
から選択される請求項2記載の液体布地柔軟化組成物。
(3) The nonionic surfactant is (i) dimethyl cocoamine oxide, (ii) nonylphenol ethoxylated with an average of 20 ethylene oxide groups per molecule, (iii) an average of 20 ethylene oxide groups per molecule. (iv) a 50/50 weight ratio of polyethylene sorbitan monolaurate and sorbitan monolaurate ethoxylated with an average of 20 ethylene oxide groups per molecule;
(v) a branched primary alcohol having 9 to 11 carbon atoms and ethoxylated with an average of 6 ethylene oxide groups per molecule; (vi) 12 to 14 carbon atoms; linear primary alcohols having atoms and ethoxylated with an average of 4, 7, 11, 13 or 23 ethylene oxide groups per molecule, and (vii) having 13 to 15 carbon atoms and per molecule 3. The liquid fabric softening composition of claim 2, wherein the liquid fabric softening composition is selected from the group consisting of branched chain primary alcohols ethoxylated with an average of 7, 8 or 11 ethylene oxide groups per ethylene oxide group.
(4)非イオン型表面活性剤の量が0.1〜4.5重量
%である請求項1記載の液体布地柔軟化組成物。
4. The liquid fabric softening composition of claim 1, wherein the amount of nonionic surfactant is from 0.1 to 4.5% by weight.
(5)陽イオン型布地柔軟剤と非イオン型表面活性剤と
のモル比が18:1〜3:1の範囲である請求項1記載
の液体布地柔軟化組成物。
5. The liquid fabric softening composition of claim 1, wherein the molar ratio of cationic fabric softener to nonionic surfactant ranges from 18:1 to 3:1.
(6)陽イオン型布地柔軟剤と脂肪酸とのモル比が少な
くとも1:1である請求項1記載の液体布地柔軟化組成
物。
6. The liquid fabric softening composition of claim 1, wherein the molar ratio of cationic fabric softener to fatty acid is at least 1:1.
(7)少なくとも1%の陽イオン型布地柔軟剤と8%未
満の脂肪酸とを含む請求項1記載の液体布地柔軟化組成
物。
7. The liquid fabric softening composition of claim 1, comprising at least 1% cationic fabric softener and less than 8% fatty acid.
JP63044066A 1987-02-27 1988-02-26 Cloth softening composition Pending JPS63282373A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB878704711A GB8704711D0 (en) 1987-02-27 1987-02-27 Fabric softening composition
GB8704711 1987-02-27

Publications (1)

Publication Number Publication Date
JPS63282373A true JPS63282373A (en) 1988-11-18

Family

ID=10613088

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63044066A Pending JPS63282373A (en) 1987-02-27 1988-02-26 Cloth softening composition

Country Status (12)

Country Link
EP (1) EP0280550B1 (en)
JP (1) JPS63282373A (en)
KR (1) KR910009652B1 (en)
AU (1) AU614073B2 (en)
BR (1) BR8800833A (en)
CA (1) CA1291302C (en)
DE (1) DE3860842D1 (en)
ES (1) ES2018338B3 (en)
GB (1) GB8704711D0 (en)
MY (1) MY103215A (en)
TR (1) TR24515A (en)
ZA (1) ZA881382B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0327180A (en) * 1989-06-19 1991-02-05 Unilever Nv Fabric softening agent
JPH04222279A (en) * 1990-12-19 1992-08-12 Dainichiseika Color & Chem Mfg Co Ltd Soft finishing agent composition
JPH05106166A (en) * 1991-03-25 1993-04-27 Unilever Nv Fiber product softened composition and manufacture of said composition
JPH05195434A (en) * 1991-07-15 1993-08-03 Unilever Nv Woven fabric softening agent
JP2019525022A (en) * 2016-08-31 2019-09-05 ザ プロクター アンド ギャンブル カンパニーThe Procter & Gamble Company Fabric enhancing composition
JP2021512233A (en) * 2018-02-28 2021-05-13 ザ プロクター アンド ギャンブル カンパニーThe Procter & Gamble Company Fabric enhancement composition

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GB8818593D0 (en) * 1988-08-04 1988-09-07 Albright & Wilson Fabric conditioners
US5484540A (en) * 1991-03-08 1996-01-16 The Procter & Gamble Company Concentrated fabric softening compositions
US5409621A (en) * 1991-03-25 1995-04-25 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening composition
CA2108905A1 (en) * 1991-04-30 1992-10-31 Alice Marie Vogel Fabric softener containing substituted imidazoline and highly ethoxylated compounds
AU4320193A (en) * 1992-06-02 1993-12-30 Unilever Plc Liquid cleaning products
HU221140B1 (en) * 1994-04-07 2002-08-28 Unilever Nv Fabric softening composition
US5503756A (en) * 1994-09-20 1996-04-02 The Procter & Gamble Company Dryer-activated fabric conditioning compositions containing unsaturated fatty acid
NZ286025A (en) * 1995-03-01 1997-04-24 Colgate Palmolive Co Laundry detergent concentrates; contains nonionic surfactant and water insoluble oil with a hydrophilic polar group, converts to liquid crystal phase dispersion on dilution
US6221828B1 (en) 1999-02-12 2001-04-24 Kao Corporation Detergent composition comprising an alkylpolyglycoside, a germicide, and a fatty acid salt
GB9930430D0 (en) * 1999-12-22 2000-02-16 Unilever Plc A method of preparing fabric softening compositions
GB0014891D0 (en) 2000-06-16 2000-08-09 Unilever Plc Fabric softening compositions
KR100591100B1 (en) * 2000-06-26 2006-06-19 주식회사 코오롱 A spinfinish oil for thermo-plastic synthetics yarn
WO2012052349A1 (en) 2010-10-22 2012-04-26 Unilever Plc Improvements relating to fabric conditioners
ES2533707T3 (en) 2010-12-03 2015-04-14 Unilever N.V. Tissue conditioners
WO2012072368A1 (en) 2010-12-03 2012-06-07 Unilever Plc Ifabric conditioners
BR112013013372A2 (en) 2010-12-03 2016-09-06 Unilever Nv preparation process of aqueous tissue conditioning composition and aqueous tissue conditioning composition

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0327180A (en) * 1989-06-19 1991-02-05 Unilever Nv Fabric softening agent
JPH04222279A (en) * 1990-12-19 1992-08-12 Dainichiseika Color & Chem Mfg Co Ltd Soft finishing agent composition
JPH05106166A (en) * 1991-03-25 1993-04-27 Unilever Nv Fiber product softened composition and manufacture of said composition
JPH05195434A (en) * 1991-07-15 1993-08-03 Unilever Nv Woven fabric softening agent
JP2019525022A (en) * 2016-08-31 2019-09-05 ザ プロクター アンド ギャンブル カンパニーThe Procter & Gamble Company Fabric enhancing composition
JP2021512233A (en) * 2018-02-28 2021-05-13 ザ プロクター アンド ギャンブル カンパニーThe Procter & Gamble Company Fabric enhancement composition

Also Published As

Publication number Publication date
EP0280550A2 (en) 1988-08-31
KR910009652B1 (en) 1991-11-25
GB8704711D0 (en) 1987-04-01
AU614073B2 (en) 1991-08-22
TR24515A (en) 1991-11-12
AU1206788A (en) 1988-09-01
CA1291302C (en) 1991-10-29
BR8800833A (en) 1988-10-04
KR880010184A (en) 1988-10-07
ES2018338B3 (en) 1991-04-01
MY103215A (en) 1993-05-29
EP0280550A3 (en) 1989-03-29
DE3860842D1 (en) 1990-11-29
EP0280550B1 (en) 1990-10-24
ZA881382B (en) 1989-10-25

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