JPH05106166A - Fiber product softened composition and manufacture of said composition - Google Patents
Fiber product softened composition and manufacture of said compositionInfo
- Publication number
- JPH05106166A JPH05106166A JP4067575A JP6757592A JPH05106166A JP H05106166 A JPH05106166 A JP H05106166A JP 4067575 A JP4067575 A JP 4067575A JP 6757592 A JP6757592 A JP 6757592A JP H05106166 A JPH05106166 A JP H05106166A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- weight
- composition according
- nonionic
- quaternary ammonium
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic compounds
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
-
- 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
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- 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
- C11D1/72—Ethers of polyoxyalkylene glycols
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)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
【0001】本発明は繊維製品柔軟化組成物に係わり、
特に、濯ぎ液に添加する繊維製品柔軟化組成物として用
いるのに適当である、非水溶性のカチオン性繊維製品柔
軟剤とノニオン性安定剤とを含有する生分解性の繊維製
品柔軟化組成物の水性分散液に係わる。The present invention relates to a textile softening composition,
In particular, a biodegradable textile softening composition containing a water-insoluble cationic textile softening agent and a nonionic stabilizer, which is suitable for use as a textile softening composition to be added to a rinsing solution. Of the aqueous dispersion of
【0002】濯ぎ液に添加する繊維製品柔軟化組成物は
公知である。この種の組成物は典型的には、水中に分散
させた非水溶性の第四アンモニウム繊維製品柔軟剤を該
柔軟剤のレベルが7重量%以下となる量か、または7〜
50重量%となる量で含有し、その際柔軟剤含量が前者
の組成物は稀釈物と看做され、後者の組成物は濃縮物と
看做される。繊維製品柔軟化組成物は、望ましくは柔軟
化以外の効果も発揮する。そのような効果の一つに、繊
維製品、特にポリエステル繊維から成る織物によごれ放
出特性を付与する効果が有る。Textile softening compositions for addition to rinse liquors are known. Compositions of this type typically contain water-insoluble quaternary ammonium textile softeners dispersed in water in an amount such that the level of softener is less than or equal to 7% by weight, or
The content of 50% by weight, the softener content being considered as a dilution of the former composition and of the latter composition as a concentrate. The textile softening composition desirably exerts effects other than softening. One such effect is to impart dirt release properties to textiles, especially textiles made of polyester fibers.
【0003】繊維製品柔軟化組成物に関連する問題の一
つとして、このような組成物の貯蔵時の物理的不安定性
が挙げられる。この問題は、組成物が濃縮物である場
合、及び貯蔵が低温で行なわれる場合に深刻化する。One of the problems associated with textile softening compositions is the physical instability of such compositions during storage. This problem is exacerbated when the composition is a concentrate and when storage is performed at low temperatures.
【0004】しかし、濃縮物であってしかも低温で安定
に貯蔵できることが消費者の要望である。物理的不安定
性は貯蔵時、組成物が流動不能となり、更には非可逆的
ゲル状にもなりかねないようなレベルまで粘稠化する事
態として現われる。粘稠化は、組成物が好ましく用いら
れることを不可能にしてしまうので甚だ望ましくない。However, it is a consumer's desire that the concentrate can be stably stored at a low temperature. Physical instability manifests itself as a composition which, upon storage, thickens to a level such that the composition becomes non-flowable and may even become an irreversible gel. Thickening is highly undesirable as it makes it impossible for the composition to be preferably used.
【0005】過去に、濯ぎ液に添加する繊維製品柔軟化
組成物の物理的安定性は、粘度調整剤もしくはゲル化防
止剤の添加によって改善された。例えばヨーロッパ特許
第13780号(Procter & Gamble)
では、幾つかの濃縮組成物に粘度調整剤を添加する。こ
の粘度調整剤はC10〜C18脂肪アルコールを含有し得
る。最近、ヨーロッパ特許第280550号(Unil
ever)において、生分解性のエステル結合第四アン
モニウム化合物と脂肪酸とを含有する稀釈組成物の物理
的安定性をノニオン界面活性剤の添加によって改善する
ことが提案されている。In the past, the physical stability of textile softening compositions added to rinses has been improved by the addition of viscosity modifiers or anti-gelling agents. For example, European Patent No. 13780 (Procter & Gamble).
Now, a viscosity modifier is added to some concentrated compositions. The viscosity modifier may contain C 10 -C 18 fatty alcohols. Recently, European Patent No. 280550 (Unil
EVER) it has been proposed to improve the physical stability of diluted compositions containing a biodegradable ester linked quaternary ammonium compound and a fatty acid by the addition of a nonionic surfactant.
【0006】生分解性のエステル結合第四アンモニウム
化合物を含有する濃縮組成物では、物理的不安定性の問
題は従来の第四アンモニウム化合物を含有する組成物の
場合よりも重大である。In concentrated compositions containing biodegradable ester-bonded quaternary ammonium compounds, the problem of physical instability is more severe than in compositions containing conventional quaternary ammonium compounds.
【0007】ヨーロッパ特許第0 040 562号
(Lesieur Cotelle)では、エステル結
合第四アンモニウム化合物を含有する濃縮物にノニオン
性の乳化剤/安定剤を添加して粘稠ゲルを生成する。用
いる安定剤は、酸化エチレン9分子でエトキシル化した
C12〜C14アルコールである。しかし、アルコールの枝
分かれの程度については言及されていない。In EP 0 040 562 (Lesieur Cotelle), a nonionic emulsifier / stabilizer is added to a concentrate containing an ester linked quaternary ammonium compound to form a viscous gel. Stabilizers used are C 12 -C 14 alcohol ethoxylated with ethylene oxide 9 molecules. However, no mention is made of the degree of alcohol branching.
【0008】或る種のノニオン性安定剤は、生分解性第
四アンモニウム化合物を含有する濃縮組成物を安定化す
るのみでなく環境に優しくもあり、即ちそれらの安定剤
は許容可能な生分解性を示し、実質的に水中生活系に有
毒でない。[0008] Certain nonionic stabilizers not only stabilize concentrated compositions containing biodegradable quaternary ammonium compounds, but are also environmentally friendly, that is, they are acceptable biodegradable. It is sexually active and practically not toxic to underwater living systems.
【0009】繊維製品によごれ放出特性を付与すること
は通常、普通は高分子量ポリマーであるよごれ放出剤を
別の処理用の洗剤組成物に含有させることによって実現
する。例えばヨーロッパ特許公開第0 398 133
号(Procter & Gamble)には、繊維製
品コンディショニング組成物に含有させるカチオンポリ
マー性よごれ放出剤が開示されている。The imparting of dirt release properties to textiles is usually accomplished by including a dirt release agent, usually a high molecular weight polymer, in the detergent composition for further treatment. For example European Patent Publication No. 0 398 133
No. (Procter & Gamble) discloses cationic polymeric dirt release agents for inclusion in textile conditioning compositions.
【0010】よごれ放出剤を含有させた組成物は、配合
成分の数が増し、コストが上昇し、かつ環境的に許容さ
れにくくなるという点で不利である。Compositions containing a dirt release agent are disadvantageous in that the number of ingredients added increases, the cost increases and it becomes less environmentally acceptable.
【0011】本願出願人は今や、生分解性のエステル結
合第四アンモニウム化合物を含有する繊維製品柔軟化組
成物が繊維製品に優れたよごれ放出特性を付与し得るこ
とを発見した。Applicants have now discovered that textile softening compositions containing biodegradable, ester linked quaternary ammonium compounds can impart excellent dirt release properties to textiles.
【0012】即ち、本発明はその一態様において、非水
溶性のカチオン性繊維製品柔軟剤とノニオン性安定剤と
を含有する繊維製品柔軟化組成物を提供し、この組成物
は前記繊維製品柔軟剤が少なくとも一つのエステル結合
を有する生分解性の第四アンモニウム物質であること、
及びノニオン性安定剤が i) 10〜20モルの酸化アルキレンでアルコキシル
化した直鎖C8〜C22アルコール、または ii) C10〜C20アルコールもしくはその混合物 であることを特徴とする。That is, the present invention provides, in one aspect thereof, a textile softening composition containing a water-insoluble cationic textile softener and a nonionic stabilizer, which composition comprises The agent is a biodegradable quaternary ammonium material having at least one ester bond,
And wherein the nonionic stabilizing agent is i) from 10 to 20 mol linear C 8 -C 22 alcohol alkoxylated with an alkylene oxide or ii) C 10 ~C 20 alcohol or mixtures thereof.
【0013】ノニオン性安定剤は、10〜20モルの酸
化アルキレンでアルコキシル化した直鎖C8〜C22アル
コールである方が有利である。[0013] nonionic stabilizer is more advantageous is alkoxylated linear C 8 -C 22 alcohol 10 to 20 moles of alkylene oxide.
【0014】好ましくは、本発明の組成物は水性ベース
から成る液体である。Preferably, the composition of the present invention is a liquid which comprises an aqueous base.
【0015】本発明の繊維製品柔軟化組成物が含有する
非水溶性のカチオン性繊維製品柔軟剤は、一つ以上のエ
ステル結合を介してN原子と結合した2個のC12〜C28
アルキルまたはアルケニル基を有する化合物であること
が有利である。The water-insoluble cationic fabric softener contained in the fabric softening composition of the present invention comprises two C 12 -C 28 linked to the N atom via one or more ester bonds.
Advantageously, it is a compound having an alkyl or alkenyl group.
【0016】本発明による組成物中に好ましく用い得る
エステル結合第四アンモニウム物質は、式Ester-bonded quaternary ammonium materials which may preferably be used in the composition according to the invention have the formula
【0017】[0017]
【化1】 [Chemical 1]
【0018】によって表わすことができる〔式中2個の
基R1はC1〜C4アルキル、アルケニル及びヒドロキシ
アルキル基の中から互いに独立に選択され、また2個の
基R2はC8〜C28アルキル及びアルケニル基の中から互
いに独立に選択され、TはThe radicals R 1, which can be [2 wherein the be represented by is selected independently of one another from among C 1 -C 4 alkyl, alkenyl and hydroxyalkyl groups and two radicals R 2 are C 8 ~ Independently selected from C 28 alkyl and alkenyl groups, T is
【0019】[0019]
【化2】 [Chemical 2]
【0020】またはOr
【0021】[0021]
【化3】 [Chemical 3]
【0022】であり、nは0〜5の整数である〕。And n is an integer of 0-5].
【0023】式Expression
【0024】[0024]
【化4】 [Chemical 4]
【0025】〔式中R1、n及びR2は先に規定したとお
りである〕によって表わせる化合物も第二の好ましい第
四アンモニウム物質である。Compounds represented by the formula wherein R 1 , n and R 2 are as defined above are also second preferred quaternary ammonium substances.
【0026】上記のような好ましい物質とその製法と
は、例えば米国特許第4 137 180号(Leve
r Brothers)に開示されている。好ましく
は、上記物質は米国特許第4 137 180号に開示
されているような対応するモノエステル、即ち例えば1
−タロウオキシ,2−ヒドロキシトリメチルアンモニウ
ムプロパンクロリドを少量含む。The above-mentioned preferable substances and the production method thereof are described in, for example, US Pat. No. 4,137,180 (Leve).
r Brothers). Preferably, the material is the corresponding monoester as disclosed in U.S. Pat. No. 4,137,180, ie 1
A small amount of tallowoxy, 2-hydroxytrimethylammonium propane chloride.
【0027】エステル結合第四アンモニウム化合物のレ
ベルは好ましくは組成物の1重量%以上で、更に好まし
くは3重量%を上回り、7重量%より多量のエステル結
合第四アンモニウム化合物を含有する濃縮組成物が特に
好ましい。エステル結合第四アンモニウム化合物のレベ
ル範囲は好ましくは1〜80重量%、更に好ましくは3
〜50重量%で、最も好ましいのは8〜50重量%であ
る。The concentration of the ester-bonded quaternary ammonium compound is preferably at least 1% by weight of the composition, more preferably above 3% by weight and containing more than 7% by weight of the ester-bonded quaternary ammonium compound. Is particularly preferable. The level range of ester-bonded quaternary ammonium compounds is preferably from 1 to 80% by weight, more preferably 3%.
˜50 wt%, most preferred is 8-50 wt%.
【0028】本発明の組成物に用い得る適当なノニオン
性安定剤として、C8〜C22第一直鎖アルコールと10
〜20モルの酸化エチレンとの縮合物が挙げられる。本
明細書中で“直鎖アルコール”という語は、炭化水素主
鎖構造に直接結合した第一アルコールを意味する。上記
酸化エチレンの用量が10モル未満であると、特にアル
キル鎖がタロウ(獣脂)範囲内に有る場合、安定剤の水
生生物毒性(aquatic toxicity)が許
容不能に増大してしまう。安定剤の水生生物毒性は酸化
エチレンのモル数とアルキル鎖の長さとの両方に関連す
るので、水生生物毒性の指標としてHLB値を用い得る
ことが判明した。HLBが約12より大きいと、1mg
/lを上回る許容不能な急性水生生物毒性値(ミジンコ
及び藻類に関してはEC5048時間であり、魚類に関し
てはEC5096時間である)がもたらされる。直鎖アル
コールを選択し、かつ20モル以下の酸化エチレンを用
いることによって、許容可能な生分解性を有するノニオ
ン性安定剤を得ることができる。しかし、20を越える
酸化エチレン単位を含むノニオン性安定剤を用いても安
定性には有益であろう。アルコールは飽和でも不飽和で
もよい。いずれもHoechst AGから入手可能な
Genapol T−110、Genapol T−1
50、Genapol T−200及びGenapol
C−200、BASFのLutensol AT1
8、HoechstのGenapolO−100及びG
enapol O−150、または、例えばAlbri
ght& WilsonのLaurex CSやShe
rexのAdol 340といった脂肪アルコールが好
ましい。好ましくは、ノニオン性安定剤のHLBは10
〜20であり、12〜20であれば更に好ましい。Suitable nonionic stabilizers which may be used in the compositions of the present invention include C 8 to C 22 primary straight chain alcohols and 10
-20 mol of ethylene oxide and a condensate are mentioned. As used herein, the term "straight chain alcohol" means a primary alcohol directly attached to the hydrocarbon backbone structure. If the dose of ethylene oxide is less than 10 mol, the aquatic toxicity of the stabilizer is unacceptably increased, especially when the alkyl chains are in the tallow range. Since the aquatic toxicity of the stabilizer is related to both the number of moles of ethylene oxide and the length of the alkyl chain, it has been found that the HLB value can be used as an indicator of aquatic toxicity. If HLB is greater than about 12, 1 mg
An unacceptable acute aquatic toxicity value of> 1/1 is obtained (EC 50 48 hours for Daphnia and algae, EC 50 96 hours for fish). By choosing a straight chain alcohol and using 20 moles or less of ethylene oxide, a nonionic stabilizer having acceptable biodegradability can be obtained. However, the use of nonionic stabilizers containing more than 20 ethylene oxide units would also be beneficial for stability. The alcohol may be saturated or unsaturated. Both are available from Hoechst AG, such as Genapol T-110 and Genapol T-1.
50, Genapol T-200 and Genapol
C-200, Lutensol AT1 from BASF
8, Hoechst Genapol O-100 and G
enapol O-150, or, for example, Albri
Laurex CS and She by ght & Wilson
A fatty alcohol such as Adol 340 from rex is preferred. Preferably, the nonionic stabilizer has an HLB of 10
-20, and more preferably 12-20.
【0029】ノニオン性安定剤のレベルは好ましくは
0.1〜10重量%、更に好ましくは0.5〜5重量%
であり、1〜4重量%が最も好ましい。第四アンモニウ
ム化合物対ノニオン性安定剤のモル比は40:1から約
1:1で、好ましくは18:1から約3:1である。The level of nonionic stabilizer is preferably 0.1 to 10% by weight, more preferably 0.5 to 5% by weight.
And 1 to 4% by weight is the most preferable. The molar ratio of quaternary ammonium compound to nonionic stabilizer is 40: 1 to about 1: 1 and preferably 18: 1 to about 3: 1.
【0030】本発明の組成物には、例えばC8〜C24ア
ルキルまたはアルケニルモノカルボン酸やそのポリマー
のような脂肪酸も含有させ得る。好ましくは飽和脂肪
酸、特に硬化獣脂C16〜C18脂肪酸を用いる。脂肪酸は
好ましくは未鹸化であり、更に好ましくは例えばオレイ
ン酸、ラウリン酸または獣脂脂肪酸を含まない。The composition of the present invention may also contain fatty acids such as C 8 to C 24 alkyl or alkenyl monocarboxylic acids and polymers thereof. Preferably saturated fatty acids, in particular use a curing tallow C 16 -C 18 fatty acids. The fatty acids are preferably unsaponified and more preferably free of eg oleic acid, lauric acid or tallow fatty acids.
【0031】脂肪酸物質のレベルは好ましくは0.1重
量%を上回り、更に好ましくは0.2重量%を上回る。
0.5〜20重量%、特に1〜10重量%の脂肪酸を含
有する濃縮物が特に好ましい。第四アンモニウム物質対
脂肪酸物質の重量比は、好ましくは10:1から1:1
0である。The level of fatty acid material is preferably above 0.1% by weight, more preferably above 0.2% by weight.
Particularly preferred are concentrates containing 0.5 to 20% by weight, especially 1 to 10% by weight of fatty acids. The weight ratio of quaternary ammonium material to fatty acid material is preferably 10: 1 to 1: 1.
It is 0.
【0032】本発明の組成物は2.0より大きいpHを
有することが好ましく、その際pHが5より小さければ
更に好ましい。The composition of the present invention preferably has a pH of greater than 2.0, more preferably a pH of less than 5.
【0033】本発明の組成物には、非水性溶剤、pH緩
衝剤、香料、香料キャリヤ、蛍光剤、着色剤、ヒドロト
ロープ、消泡剤、再付着防止剤、酵素、蛍光増白剤、不
透明剤、防縮剤、皺防止剤、染み防止剤、殺菌剤、殺黴
剤、酸化防止剤、防食剤、襞付け剤、帯電防止剤及びア
イロン掛け補助剤の中から選択した1種以上の任意成分
も含有させ得る。The compositions of the present invention include non-aqueous solvents, pH buffers, fragrances, fragrance carriers, fluorescent agents, colorants, hydrotropes, defoamers, anti-redeposition agents, enzymes, optical brighteners, opaque agents. One or more optional ingredients selected from agents, anti-shrinking agents, anti-wrinkling agents, stain-proofing agents, bactericides, fungicides, antioxidants, anticorrosives, folds, antistatic agents and ironing aids Can also be included.
【0034】本発明の組成物には、ラノリンとその誘導
体のようなノニオン性の繊維製品柔軟剤を含有させるこ
とも可能である。The compositions of the present invention can also include nonionic textile softeners such as lanolin and its derivatives.
【0035】[0035]
【実施例】本発明を、以下の非限定的な実施例によって
詳述する。各実施例において、組成百分率は総て重量に
基づく。The present invention is illustrated by the following non-limiting examples. In each example, all compositional percentages are by weight.
【0036】実施例1 液状の繊維製品柔軟化組成物を次のように製造した。 Example 1 A liquid textile softening composition was prepared as follows.
【0037】カチオン性繊維製品柔軟剤と、脂肪酸と、
更に適宜にノニオン性安定剤とを予め混合し、かつ一緒
に加熱して、透明な溶融体を製造した。このように製造
した溶融混合物を70〜80℃の水に、一定の攪拌下に
少なくとも1分掛けて添加して、分散液を製造した。Cationic textile softener, fatty acid,
Furthermore, if appropriate, a nonionic stabilizer was premixed and heated together to produce a transparent melt. The thus-prepared molten mixture was added to water at 70 to 80 ° C. over a period of at least 1 minute with constant stirring to prepare a dispersion liquid.
【0038】得られた組成物の粘度を、周囲温度または
5℃で21日間貯蔵後にHaake回転式粘度計(ro
toviscometer)で測定した。The viscosity of the resulting composition was measured by a Haake rotary viscometer (ro) after storage for 21 days at ambient or 5 ° C.
It was measured by a toviscomter).
【0039】 組成物 A B C D E F G 成分 Arquad 2HT1) 12.8 − − − − − − HT TMAPC2) − 16 16 16 16 11.6 12.6 脂肪酸3) 3.2 2.7 2.7 2.7 2.7 1.9 2.
1 獣脂11EO4) − 3 − − − − − ヤシ油10EO5) − − 2 − − − − 獣脂20EO6) − − − 3 − − − アルコール7) − − − − − 1.5 1.5 水+微量物質 全体を100とする量110s -1 での粘度(mPa) 周囲温度 159 77 34 43 90 53 50 5℃ 155 66 38 47 ゲル 50 50 注記:組成物Aは、現在英国でLeverにより商標“COMFOR
T”の下に市販されている繊維製品柔軟化組成物に対応
する。Composition A B C D E F G component Arquad 2HT 1) 12.8 − − − − − − HT TMAPC 2) − 16 16 16 16 11.6 12.6 Fatty acid 3) 3.2 2.7 2.7 2.7 2.7 1.9 2.
1 Tallow 11EO 4) − 3 − − − − − Palm oil 10EO 5) − − 2 − − − − Tallow 20EO 6) − − − 3 − − − Alcohol 7) − − − − − 1.5 1.5 Water + Trace substances Viscosity at 110 s -1 (mPa) Ambient temperature 159 77 34 43 90 53 50 5 ° C 155 66 38 47 Gel 50 50 Note: Composition A is currently under the trademark "COMFOR" by Lever in the United Kingdom.
Corresponds to the textile softening composition marketed under T ".
【0040】1); Arquad 2HTは、Akzo Chemieから入手
可能なジ硬化獣脂ジメチルアンモニウムクロリドであ
る。 1) ; Arquad 2HT is a di-hardened tallow dimethylammonium chloride available from Akzo Chemie.
【0041】2); HT TMAPCは、Hoechstから入手可能な
1,2ジ硬化タロウイルオキシ−3−トリメチル−アンモニ
オプロパンクロリドである。 2) ; HT TMAPC is available from Hoechst
1,2 di-cured tallowyloxy-3-trimethyl-ammoniopropane chloride.
【0042】3); Unichemaから入手可能な硬化獣脂脂
肪酸Pristerine 4916。 3) ; Hardened tallow fatty acid Pristerine 4916 available from Unichema.
【0043】4); 11モルの酸化エチレンでエトキシル
化した獣脂アルコールで、HLB13。 4) ; tallow alcohol ethoxylated with 11 moles of ethylene oxide, HLB13.
【0044】5); 10モルの酸化エチレンでエトキシル
化したヤシ油アルコールで、HLB14。 5) ; Coconut oil alcohol ethoxylated with 10 moles of ethylene oxide, HLB14.
【0045】6); 20モルの酸化エチレンでエトキシル
化した獣脂アルコールで、HLB20。 6) ; TLB alcohol ethoxylated with 20 moles of ethylene oxide, HLB20.
【0046】7); Albright & Wilsonから入手可能であ
る、65〜80%のC18及び20〜23%のC16を含有する獣脂ア
ルコールLaurex CS。 7) ; Laurex CS, tallow alcohol containing 65-80% C 18 and 20-23% C 16 , available from Albright & Wilson.
【0047】測定結果は、5℃での短期貯蔵で、通常の
第四アンモニウム化合物を含有する公知の繊維製品柔軟
化組成物(組成物A)が物理的不安定性を示さない一方
で、エステル結合第四アンモニウム化合物及び脂肪酸を
含有する組成物(組成物E)では問題が生起することを
示している。また、選択したノニオン性安定剤の添加に
よって安定性の低下が阻止でき、安定な濃縮組成物が得
られることも、上記の結果から明らかである。The results of the measurement show that the known fabric softening composition (composition A) containing a usual quaternary ammonium compound does not show physical instability on short-term storage at 5.degree. It has been shown that problems occur with compositions containing quaternary ammonium compounds and fatty acids (Composition E). It is also clear from the above results that the addition of the selected nonionic stabilizer can prevent the stability from decreasing and a stable concentrated composition can be obtained.
【0048】実施例2 下記の組成を有する液状の繊維製品柔軟化組成物A及び
Bを、実施例1に述べた方法で製造した。得られた組成
物での処理によってポリエステル試験片に付与されるよ
ごれ放出特性を、染みを付けた試験片を有標洗剤組成物
中で洗濯した後に該試験片の反射率変化を測定すること
によって評価した。まず、試験片を、組成物AまたはB
を0.67ml含有する14°FHの水1l中で5分間
濯いだ。次に試験片を綱に吊して乾燥し、乾燥した試験
片にスダンレッド染料0.06%含有のオリーブオイル
100μlで染みを付けた。染みを最低2日間広がらせ
た後、染みを付けた試験片の反射率(R1)をICSマ
イクロマッチで測定した。その後試験片を、14°FH
の水にLeverから入手可能なNew System
Persil Automaticを5g/lの量で
用いて、15分の洗濯サイクルで洗い、濯ぎ、かつ綱に
吊して乾燥した。前処理した試験片の洗濯後の反射率
(R2)を測定し、洗浄率(%)を次の式 洗浄率(%)=[(Ks1−Ks2)/Ks1]×100 〔式中Ks1=(1−R1)2/2R1、Ks2=(1−
R2)2/2R2〕に従って計算した。 Example 2 Liquid textile softening compositions A and B having the following compositions were prepared by the method described in Example 1. The soil release properties imparted to polyester test pieces by treatment with the resulting composition were measured by measuring the reflectance change of the test piece after washing the stained test piece in a proprietary detergent composition. evaluated. First, a test piece was prepared using the composition A or B.
Was rinsed in 1 liter of 14 ° FH water containing 0.67 ml for 5 minutes. Next, the test piece was hung on a rope and dried, and the dried test piece was stained with 100 μl of olive oil containing 0.06% of Sudan red dye. After spreading the stain for a minimum of 2 days, the reflectance (R 1 ) of the stained specimen was measured by ICS Micromatch. The test piece is then placed at 14 ° FH
New System available from Lever in the water
Persil Automatic was used in an amount of 5 g / l for a 15 minute wash cycle, rinsed and hung on a rope to dry. The reflectance (R 2 ) after washing of the pretreated test piece was measured, and the washing rate (%) was calculated by the following equation: washing rate (%) = [(Ks 1 −Ks 2 ) / Ks 1 ] × 100 [Equation Medium Ks 1 = (1-R 1 ) 2 / 2R 1 , Ks 2 = (1-
R 2 ) 2 / 2R 2 ].
【0049】上記洗浄率が高いほどよごれ放出効果は大
きい。The higher the cleaning rate is, the greater the dust release effect is.
【0050】 組成物 A B 成分(重量%) Arquad 2HT1) − 12.8 HT TMAPC2) 11.6 − 脂肪酸3) 1.9 3.2 獣脂11EO4) 2.5 − 水及び微量物質 全体を100とする量洗浄率(%) 30 21 注記:組成物Bは、現在英国でLeverにより商標“COMFOR
T”の下に市販されている繊維製品柔軟化組成物に対応
する。1)、2)、3)及び4)は実施例1と同様である。The compositions A B Component (wt%) Arquad 2HT 1) - 12.8 HT TMAPC 2) 11.6 - fatty 3) 1.9 3.2 Tallow 11EO 4) 2.5 - amount detergency ratio of the entire water and trace substances and 100 (%) 30 21 Note: Composition B is currently under the trademark "COMFOR" by Lever in the United Kingdom.
It corresponds to the textile softening composition marketed under T ". 1) , 2) , 3) and 4) are the same as in Example 1.
【0051】上記結果は、通常の第四アンモニウム化合
物を含有する公知組成物(組成物B)のよごれ放出効果
の方が本発明による組成物(組成物A)のよごれ放出効
果より小さいことを示している。The above results show that the known composition containing conventional quaternary ammonium compounds (composition B) has a dirt-release effect smaller than that of the composition according to the present invention (composition A). ing.
【0052】実施例3 本発明による組成物の好ましい組成例は次のとおりであ
る。 Example 3 A preferred composition example of the composition according to the present invention is as follows.
【0053】 組成物 A B C 成分(重量%) HT TMAPC2) 11.6 11.6 11.6 脂肪酸3) 1.9 1.9 1.9 獣脂11EO4) − 2.5 − 獣脂アルコール7) 1.5 − − 獣脂15EO8) − − 1.5 イソプロピルアルコール 1.6 1.6 1.6 グリセロール 1.6 1.6 1.6 香料、染料及び微量物質 0.8 0.8 0.8 水 全体を100とする量 注記:2)、3)、4)及び7)は実施例1と同様である。The compositions A B C Component (wt%) HT TMAPC 2) 11.6 11.6 11.6 fatty acid 3) 1.9 1.9 1.9 Tallow 11EO 4) - 2.5 - tallow alcohol 7) 1.5 - - Tallow 15 EO 8) - - 1.5 Isopropyl alcohol 1.6 1.6 1.6 Glycerol 1.6 1.6 1.6 Fragrances, dyes and trace substances 0.8 0.8 0.8 Amount based on 100 as total water Note: 2) , 3) , 4) and 7) are the same as in Example 1.
【0054】8); 15モルの酸化エチレンでエトキシル
化した獣脂アルコール。 8) ; tallow alcohol ethoxylated with 15 moles of ethylene oxide.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C11D 1/72 8827−4H 3/26 8827−4H ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location C11D 1/72 8827-4H 3/26 8827-4H
Claims (10)
ノニオン性安定剤とを含有する繊維製品柔軟化組成物で
あって、前記繊維製品柔軟剤が少なくとも一つのエステ
ル結合を有する生分解性の第四アンモニウム物質であ
り、またノニオン性安定剤は i) 10〜20モルの酸化アルキレンでアルコキシル
化した直鎖C8〜C22アルコール、または ii) C10〜C20アルコールもしくはその混合物 であることを特徴とする繊維製品柔軟化組成物。1. A fabric softening composition comprising a water-insoluble cationic fabric softener and a nonionic stabilizer, wherein the fabric softener has at least one ester bond and is biodegradable. quaternary and ammonium material, also nonionic stabilizers i) is 10 to 20 mol linear C 8 -C 22 alcohol alkoxylated with an alkylene oxide or ii) C 10 ~C 20 alcohol or mixtures thereof, of A softening composition for textile products, which is characterized in that:
化アルキレンでアルコキシル化した直鎖C8〜C22アル
コールであることを特徴とする請求項1に記載の組成
物。2. A composition according to claim 1, characterized in that the nonionic stabilizer is a linear C 8 -C 22 alcohol alkoxylated with 10 to 20 mol of alkylene oxide.
上であることを特徴とする請求項1または2に記載の組
成物。3. The composition according to claim 1, wherein the quaternary ammonium substance content is 1% by weight or more.
量%であることを特徴とする請求項1から3のいずれか
1項に記載の組成物。4. The composition according to claim 1, wherein the content of the nonionic stabilizer is 0.1 to 10% by weight.
有することを特徴とする請求項1から4のいずれか1項
に記載の組成物。5. Composition according to any one of claims 1 to 4, characterized in that it also contains more than 0.1% by weight of fatty acid substances.
と、0.5〜5重量%のノニオン性安定剤と、0.5〜
20重量%の脂肪酸物質とを含有することを特徴とする
請求項1から5のいずれか1項に記載の組成物。6. A quaternary ammonium substance in an amount of 3 to 50% by weight, a nonionic stabilizer in an amount of 0.5 to 5% by weight, and 0.5 to 5% by weight.
Composition according to any one of claims 1 to 5, characterized in that it contains 20% by weight of fatty acid substances.
であることを特徴とする請求項1から6のいずれか1項
に記載の組成物。7. The nonionic stabilizer has an HLB of 10 to 20.
The composition according to any one of claims 1 to 6, wherein
であることを特徴とする請求項7に記載の組成物。8. The nonionic stabilizer has an HLB of 12 to 20.
The composition according to claim 7, which is:
一つ以上のエステル結合を介してN原子と結合した2個
のC12〜C28アルキルまたはアルケニル基を有する化合
物を含むことを特徴とする請求項1から8のいずれか1
項に記載の組成物。9. A water-insoluble cationic textile softener comprising a compound having two C 12 -C 28 alkyl or alkenyl groups linked to N atoms via one or more ester bonds. Any one of claims 1 to 8
The composition according to the item.
の液状の繊維製品柔軟化組成物を製造する方法であっ
て、 i) カチオン性繊維製品柔軟剤とノニオン性安定剤と
を混合及び加熱して溶融体を製造するステップ、及び ii) 前記溶融体を水中に分散させるステップ を含む繊維製品柔軟化組成物製造方法。10. A method for producing a liquid textile softening composition according to any one of claims 1 to 9, wherein i) a cationic textile softener and a nonionic stabilizer are mixed. And a step of producing a melt by heating, and ii) a step of dispersing the melt in water.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9106308.1 | 1991-03-25 | ||
GB919106308A GB9106308D0 (en) | 1991-03-25 | 1991-03-25 | Fabric softening composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05106166A true JPH05106166A (en) | 1993-04-27 |
JP2937306B2 JP2937306B2 (en) | 1999-08-23 |
Family
ID=10692165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4067575A Expired - Fee Related JP2937306B2 (en) | 1991-03-25 | 1992-03-25 | Textile softening composition and method for producing the composition |
Country Status (9)
Country | Link |
---|---|
EP (2) | EP0506312B1 (en) |
JP (1) | JP2937306B2 (en) |
AU (1) | AU652429B2 (en) |
BR (1) | BR9201017A (en) |
CA (1) | CA2063463C (en) |
DE (2) | DE69207624T2 (en) |
ES (2) | ES2088542T3 (en) |
GB (1) | GB9106308D0 (en) |
ZA (1) | ZA922173B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7179783B2 (en) | 2002-04-17 | 2007-02-20 | Kao Corporation | Sulfuric acid amine salt, sulfonic acid amine salt, production thereof and softener composition |
JP2007508126A (en) * | 2003-10-16 | 2007-04-05 | ザ プロクター アンド ギャンブル カンパニー | Aqueous composition comprising vesicles having specific vesicle permeability |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9115255D0 (en) * | 1991-07-15 | 1991-08-28 | Unilever Plc | Fabric softening composition |
GB9301728D0 (en) * | 1993-01-28 | 1993-03-17 | Unilever Plc | Fabric softening composition |
DE69325578T3 (en) * | 1992-05-12 | 2004-06-03 | The Procter & Gamble Company, Cincinnati | CONCENTRATED LIQUID TISSUE SOFTENER COMPOSITIONS WITH BIODEGRADABLE TISSUE SOFTENERS |
WO1993025648A1 (en) * | 1992-06-10 | 1993-12-23 | The Procter & Gamble Company | Stable biodegradable fabric softening compounds and compositions |
CA2157178C (en) * | 1993-03-01 | 2002-08-20 | Errol Hoffman Wahl | Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains |
US5750491A (en) * | 1993-08-02 | 1998-05-12 | The Procter & Gamble Company | Super concentrate emulsions with fabric actives |
US6559117B1 (en) | 1993-12-13 | 2003-05-06 | The Procter & Gamble Company | Viscosity stable concentrated liquid fabric softener compositions |
US5413723A (en) * | 1993-12-17 | 1995-05-09 | Munteanu; Marina A. | Use of special surfactants to control viscosity in fabric softeners |
EP0754215B1 (en) * | 1994-04-07 | 2001-05-23 | Unilever Plc | Fabric softening composition |
GB9406824D0 (en) * | 1994-04-07 | 1994-06-01 | Unilever Plc | Fabric softening composition |
AU2399295A (en) * | 1994-04-29 | 1995-11-29 | Procter & Gamble Company, The | Cellulase fabric-conditioning compositions |
MA23554A1 (en) * | 1994-05-18 | 1995-12-31 | Procter & Gamble | SOFTENING COMPOSITIONS FOR BIODEGRADABLE AND CONCENTRATED QUATERNARY AMMONIUM BASED LAUNDRY CONTAINING QUATERNARY AMMONIUM COMPOUNDS WITH SHORT FATTY ACID ALKYL CHAINS |
US5445747A (en) * | 1994-08-05 | 1995-08-29 | The Procter & Gamble Company | Cellulase fabric-conditioning compositions |
US5503756A (en) * | 1994-09-20 | 1996-04-02 | The Procter & Gamble Company | Dryer-activated fabric conditioning compositions containing unsaturated fatty acid |
US5460736A (en) * | 1994-10-07 | 1995-10-24 | The Procter & Gamble Company | Fabric softening composition containing chlorine scavengers |
US5474690A (en) * | 1994-11-14 | 1995-12-12 | The Procter & Gamble Company | Concentrated biodegradable quaternary ammonium fabric softener compositions containing intermediate iodine value fatty acid chains |
GB9503596D0 (en) * | 1995-02-23 | 1995-04-12 | Unilever Plc | Cleaning composition comprising quaternised poly-dimethylsiloxane and nonionic surfactant |
GB9517433D0 (en) * | 1995-08-25 | 1995-10-25 | Unilever Plc | Soil release agent and its use in fabric conditioning compositions |
GB9526182D0 (en) * | 1995-12-21 | 1996-02-21 | Unilever Plc | Fabric softening composition |
GB2313379A (en) * | 1996-05-23 | 1997-11-26 | Unilever Plc | A detergent composition comprising perfume |
BR9701287A (en) * | 1997-03-14 | 1998-11-10 | Unilever Nv | Fabric treatment composition in washing and process to treat fabrics to provide them with dirt repellent properties |
GB0121802D0 (en) | 2001-09-10 | 2001-10-31 | Unilever Plc | Fabric conditioning compositions |
US7655609B2 (en) | 2005-12-12 | 2010-02-02 | Milliken & Company | Soil release agent |
US9926516B2 (en) | 2014-06-05 | 2018-03-27 | The Procter & Gamble Company | Mono alcohols for low temperature stability of isotropic liquid detergent compositions |
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-
1991
- 1991-03-25 GB GB919106308A patent/GB9106308D0/en active Pending
-
1992
- 1992-03-19 CA CA002063463A patent/CA2063463C/en not_active Expired - Lifetime
- 1992-03-20 DE DE69207624T patent/DE69207624T2/en not_active Expired - Lifetime
- 1992-03-20 ES ES92302452T patent/ES2088542T3/en not_active Expired - Lifetime
- 1992-03-20 EP EP92302453A patent/EP0506312B1/en not_active Expired - Lifetime
- 1992-03-20 DE DE69211203T patent/DE69211203T2/en not_active Revoked
- 1992-03-20 EP EP92302452A patent/EP0507478B1/en not_active Revoked
- 1992-03-20 ES ES92302453T patent/ES2083084T3/en not_active Expired - Lifetime
- 1992-03-23 AU AU13125/92A patent/AU652429B2/en not_active Ceased
- 1992-03-24 BR BR929201017A patent/BR9201017A/en not_active IP Right Cessation
- 1992-03-25 JP JP4067575A patent/JP2937306B2/en not_active Expired - Fee Related
- 1992-03-25 ZA ZA922173A patent/ZA922173B/en unknown
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JPS63282373A (en) * | 1987-02-27 | 1988-11-18 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Cloth softening composition |
JPH01162872A (en) * | 1987-09-23 | 1989-06-27 | Procter & Gamble Co:The | Stable biodegradable cloth softening composition containing linear alkoxylated fabric |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7179783B2 (en) | 2002-04-17 | 2007-02-20 | Kao Corporation | Sulfuric acid amine salt, sulfonic acid amine salt, production thereof and softener composition |
JP2007508126A (en) * | 2003-10-16 | 2007-04-05 | ザ プロクター アンド ギャンブル カンパニー | Aqueous composition comprising vesicles having specific vesicle permeability |
Also Published As
Publication number | Publication date |
---|---|
EP0506312B1 (en) | 1996-01-17 |
JP2937306B2 (en) | 1999-08-23 |
CA2063463C (en) | 1999-04-27 |
DE69207624D1 (en) | 1996-02-29 |
EP0507478A1 (en) | 1992-10-07 |
GB9106308D0 (en) | 1991-05-08 |
AU1312592A (en) | 1992-10-01 |
DE69211203T2 (en) | 1996-10-10 |
EP0506312A1 (en) | 1992-09-30 |
DE69207624T2 (en) | 1996-05-30 |
DE69211203D1 (en) | 1996-07-11 |
ES2088542T3 (en) | 1996-08-16 |
EP0507478B1 (en) | 1996-06-05 |
ES2083084T3 (en) | 1996-04-01 |
BR9201017A (en) | 1992-11-24 |
AU652429B2 (en) | 1994-08-25 |
CA2063463A1 (en) | 1992-09-26 |
ZA922173B (en) | 1993-09-27 |
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