JPH04333667A - Liquid softening agent composition - Google Patents

Liquid softening agent composition

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Publication number
JPH04333667A
JPH04333667A JP13551591A JP13551591A JPH04333667A JP H04333667 A JPH04333667 A JP H04333667A JP 13551591 A JP13551591 A JP 13551591A JP 13551591 A JP13551591 A JP 13551591A JP H04333667 A JPH04333667 A JP H04333667A
Authority
JP
Japan
Prior art keywords
softening agent
alkyl group
quaternary ammonium
agent composition
group
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
JP13551591A
Other languages
Japanese (ja)
Other versions
JP2956274B2 (en
Inventor
Shuichi Nihei
秀一 二瓶
Katsuyuki Takeuchi
克之 竹内
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.)
Lion Corp
Original Assignee
Lion Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lion Corp filed Critical Lion Corp
Priority to JP13551591A priority Critical patent/JP2956274B2/en
Publication of JPH04333667A publication Critical patent/JPH04333667A/en
Application granted granted Critical
Publication of JP2956274B2 publication Critical patent/JP2956274B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain a liquid softening agent composition, composed of a specific quaternary ammonium salt, capable of imparting excellent softness and antistatic properties to various clothes, excellent in water absorbing and holding properties and having good biodegradability. CONSTITUTION:A liquid softening agent composition containing a quaternary ammonium salt, expressed by the formula {R<1> and R<2> are 11-23C saturated or unsaturated alkyl group; the total alkyl groups in R<1> and R<2> are within the range of (2:98)-(30:70) weight ratio of the saturated alkyl group : unsaturated alkyl group; R and R are 1-4C alkyl or hydroxyalkyl; R<5> and R<6> are CmH2m. [(m) 18 2-4]; X<-> is anion; (n) is 1-4} and having ester bonds as a base material for the softening agent. The resultant softening agent composition is capable of imparting excellent softness and antistatic properties to various fibers by its application. This softening agent composition is excellent in water absorbing and holding effects and improved in biodegradability.

Description

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

【0001】0001

【産業上の利用分野】本発明は、各種衣料へ柔軟性及び
帯電防止性を付与する効果が良好な上、吸水性保持効果
に優れ、かつ,生分解性が良好な液体柔軟剤組成物に関
する。
[Field of Industrial Application] The present invention relates to a liquid fabric softener composition that is effective in imparting flexibility and antistatic properties to various types of clothing, has an excellent water absorption retention effect, and has good biodegradability. .

【0002】0002

【従来の技術及び発明が解決しようとする課題】従来、
洗濯後の衣料に柔軟性と帯電防止性とを付与するために
各種の液体柔軟剤組成物が使用されている。これら柔軟
剤組成物としては、ジ長鎖アルキルジ短鎖アルキル第4
級アンモニウム塩を主成分としたものが一般的である。 しかし、このジ長鎖アルキルジ短鎖アルキル第4級アン
モニウム塩を配合した柔軟剤組成物は各種衣料に対して
良好な柔軟効果と帯電防止効果とを付与することができ
るものの、同時に衣料の吸水性を低下させてしまうとい
う欠点を有する。更に、生分解性に劣るために河川の汚
染の一因とされている。
[Prior art and problems to be solved by the invention] Conventionally,
Various liquid fabric softener compositions are used to impart flexibility and antistatic properties to clothing after laundering. These softener compositions include di-long-chain alkyl di-short-chain alkyl quaternary
Generally, the main component is a grade ammonium salt. However, although the fabric softener composition containing this di-long-chain alkyl di-short-chain alkyl quaternary ammonium salt can impart a good softening effect and antistatic effect to various types of clothing, it also reduces the water absorption of the clothing. It has the disadvantage of lowering the Furthermore, it is considered to be a cause of river pollution due to its poor biodegradability.

【0003】一方、最近、柔軟剤組成物の主成分として
炭素数12〜22の長鎖アルキルエステル基を有する第
4級アンモニウム塩が生分解性が良好なことから注目さ
れている(特開昭63−6168号公報記載)が、この
第4級アンモニウム塩を配合した柔軟剤組成物も上記柔
軟剤組成物と同様に柔軟性付与効果等は良好であるが、
吸水性保持の点で満足できるものではない。
On the other hand, recently, quaternary ammonium salts having a long-chain alkyl ester group with 12 to 22 carbon atoms have been attracting attention as a main component of softener compositions due to their good biodegradability (Japanese Patent Application Laid-open No. 63-6168), the softener composition containing this quaternary ammonium salt also has a good softening effect, etc., like the above-mentioned softener composition.
It is not satisfactory in terms of water absorption retention.

【0004】従って、柔軟性及び帯電防止性付与効果に
加えて、吸水性保持効果及び生分解性に優れた液体柔軟
剤組成物の開発が望まれている。
[0004]Therefore, it is desired to develop a liquid softener composition that has excellent water absorbency retaining effects and biodegradability in addition to imparting flexibility and antistatic properties.

【0005】[0005]

【課題を解決するための手段及び作用】本発明者は上記
事情に鑑み鋭意検討を重ねた結果、下記一般式(I)で
示される特定のエステル結合を有する第4級アンモニウ
ム塩を柔軟剤基剤として使用することにより、各種衣料
へ柔軟性及び帯電防止性を良好に付与し得ると共に、衣
料の吸水性を低下させることなく良好に保持し得、しか
も、生分解性に優れ、環境汚染の問題がほとんどない液
体柔軟剤組成物を得ることができることを知見し、本発
明をなすに至ったものである。
[Means and Effects for Solving the Problems] In view of the above circumstances, the present inventors have made extensive studies and found that a quaternary ammonium salt having a specific ester bond represented by the following general formula (I) has a softening agent group. By using it as an agent, it is possible to impart good flexibility and antistatic properties to various types of clothing, and it is also possible to retain water well without reducing the water absorbency of the clothing.Moreover, it has excellent biodegradability and does not cause environmental pollution. The inventors have discovered that it is possible to obtain a liquid softener composition with almost no problems, leading to the present invention.

【0006】[0006]

【化2】 〔但し、式中R1、R2はそれぞれ炭素数11〜23の
飽和又は不飽和アルキル基で、かつ、R1及びR2の総
アルキル基は飽和アルキル基:不飽和アルキル基(重量
比)が2:98〜30:70の範囲である。また、R3
、R4はそれぞれ炭素数1〜4のアルキル基又はヒドロ
キシアルキル基、R5、R6はそれぞれCmH2m(但
し、m=2〜4)であり、X−は陰イオン、nは1〜4
の数である。〕
[Formula 2] [However, in the formula, R1 and R2 are each a saturated or unsaturated alkyl group having 11 to 23 carbon atoms, and the total alkyl group of R1 and R2 is saturated alkyl group:unsaturated alkyl group (weight ratio) is in the range of 2:98 to 30:70. Also, R3
, R4 are each an alkyl group or hydroxyalkyl group having 1 to 4 carbon atoms, R5 and R6 are each CmH2m (however, m=2 to 4), X- is an anion, and n is 1 to 4
is the number of ]

【0007】以下、本発明につき更に詳細に説明すると
、本発明の液体柔軟剤組成物は、柔軟剤基剤として下記
一般式(I)で示される第4級アンモニウム塩を含有す
る。
The present invention will be explained in more detail below. The liquid softener composition of the present invention contains a quaternary ammonium salt represented by the following general formula (I) as a softener base.

【0008】[0008]

【化3】[C3]

【0009】ここで、上記(I)式中のR1、R2はそ
れぞれ炭素数11〜23、好ましくは15〜21の飽和
又は不飽和のアルキル基であり、例えばR1−CO、R
2−COで示される基が通常オレイン酸、エライジン酸
、リノール酸、リノレイン酸等の不飽和高級脂肪酸、ス
テアリン酸、パルミチン酸等の飽和高級脂肪酸、牛脂、
豚脂、パーム油、大豆油、サフラワー油、ヒマワリ油、
オリーブ油等の天然油脂を分解・精製して得られる脂肪
酸、これらの硬化脂肪酸から由来するものであるが、こ
れらの中でも特にオレイン酸、エライジン酸、ステアリ
ン酸、牛脂脂肪酸、硬化牛脂脂肪酸、パーム油脂肪酸、
硬化パーム油脂肪酸の混合物が好適である。なお、不飽
和高級脂肪酸としては立体異性構造がシス体又はトラン
ス体であっても、あるいは両者の混合物であってもよい
が、特にシス体/トランス体の比率が25〜100/0
〜75であることが好ましい。
Here, R1 and R2 in the above formula (I) are each a saturated or unsaturated alkyl group having 11 to 23 carbon atoms, preferably 15 to 21 carbon atoms, such as R1-CO, R
The group represented by 2-CO is usually unsaturated higher fatty acids such as oleic acid, elaidic acid, linoleic acid, and linoleic acid, saturated higher fatty acids such as stearic acid and palmitic acid, beef tallow,
Pork fat, palm oil, soybean oil, safflower oil, sunflower oil,
Fatty acids obtained by decomposing and refining natural fats and oils such as olive oil, and those derived from these hydrogenated fatty acids, especially oleic acid, elaidic acid, stearic acid, beef tallow fatty acid, hydrogenated beef tallow fatty acid, and palm oil fatty acid. ,
Mixtures of hydrogenated palm oil fatty acids are preferred. In addition, the stereoisomeric structure of the unsaturated higher fatty acid may be cis or trans, or a mixture of the two, but especially those with a cis/trans ratio of 25 to 100/0.
It is preferable that it is 75.

【0010】更に、R1及びR2の総アルキル基は飽和
アルキル基:不飽和アルキル基(重量比)が2:98〜
30:70、好ましくは5:95〜15:85であり、
飽和アルキル基の含有割合が30/70よりも多くなる
と柔軟剤組成物の吸水性保持効果が劣り、本発明の目的
を達成し得ない。
Furthermore, the total alkyl groups of R1 and R2 have a saturated alkyl group:unsaturated alkyl group (weight ratio) of 2:98 to
30:70, preferably 5:95 to 15:85,
If the content ratio of saturated alkyl groups is more than 30/70, the water absorption retention effect of the softener composition will be poor and the object of the present invention cannot be achieved.

【0011】また、R3、R4はそれぞれ炭素数1〜4
のアルキル基又はヒドロキシアルキル基であり、具体的
にはメチル基、エチル基、プロピル基、ブチル基、ヒド
ロキシメチル基、ヒドロキシエチル基、ヒドロキシプロ
ピル基、ヒドロキシブチル基が挙げられるが、特にメチ
ル基、エチル基、ヒドロキシエチル基が好ましく用いら
れる。R5、R6はそれぞれCmH2m(但し、m=2
〜4)で示されるアルキレン基であり、具体的にはエチ
レン基、プロピレン基、ブチレン基が挙げられ、直鎖状
でも分岐鎖状でもよい。
[0011] Furthermore, R3 and R4 each have 1 to 4 carbon atoms.
An alkyl group or hydroxyalkyl group, specific examples include methyl group, ethyl group, propyl group, butyl group, hydroxymethyl group, hydroxyethyl group, hydroxypropyl group, and hydroxybutyl group, but especially methyl group, Ethyl group and hydroxyethyl group are preferably used. R5 and R6 are each CmH2m (however, m=2
It is an alkylene group represented by ~4), and specifically includes an ethylene group, a propylene group, and a butylene group, and may be linear or branched.

【0012】更に、X−は陰イオンであり、具体的には
塩素、臭素、ヨウ素等のハロゲン原子アニオン、R7S
O4(R7は炭素数1〜3のアルキル基であり、具体的
にはメチル基、エチル基、プロピル基が挙げられるが、
特にメチル基が好適である。)で示される基のアニオン
などが例示される。
Furthermore, X- is an anion, specifically a halogen atom anion such as chlorine, bromine, iodine, R7S
O4 (R7 is an alkyl group having 1 to 3 carbon atoms, specific examples include methyl group, ethyl group, and propyl group,
Particularly suitable is a methyl group. ) are exemplified.

【0013】このような(I)式の第4級アンモニウム
塩としては、ジ(ステアロイルオキシエチル)ジメチル
4級アンモニウムクロライド、ジ(ステアロイルオキシ
ブチル)ジメチル4級アンモニウムクロライド、ジ(オ
レオイルオキシエチル)ジメチル4級アンモニウムクロ
ライド、ジ(パルミトイルオキシエチル)ジメチル4級
アンモニウムメトサルフェート、ジ(ステアロイルオキ
シイソプロピル)ジメチル4級アンモニウムクロライド
、ジ(オレオイルオキシブチル)ジメチル4級アンモニ
ウムクロライド、ジ(オレオイルオキシイソプロピル)
ジメチル4級アンモニウムメトサルフェート、ジ(エラ
イジオイルオキシエチル)ジメチル4級アンモニウムク
ロライド、(ステアロイルオキシエチル)(オレオイル
オキシエチル)ジメチル4級アンモニウムクロライド、
(ステアロイルオキシイソプロピル)(オレオイルオキ
シイソプロピル)ジメチル4級アンモニウムメトサルフ
ェート、(パルミトイルオキシエチル)(オレオイルオ
キシエチル)ジメチル4級アンモニウムクロライド、(
ステアロイルオキシイソプロピル)(エライジオイルオ
キシイソプロピル)ジメチル4級アンモニウムメトサル
フェト、(ステアロイルオキシブチル)(オレオイルオ
キシブチル)ジメチル4級アンモニウムクロライド等が
例示され、これらの1種類を単独で使用しても、2種類
以上を混合して使用してもよい。
Such quaternary ammonium salts of formula (I) include di(stearoyloxyethyl)dimethyl quaternary ammonium chloride, di(stearoyloxybutyl)dimethyl quaternary ammonium chloride, di(oleoyloxyethyl) Dimethyl quaternary ammonium chloride, di(palmitoyloxyethyl) dimethyl quaternary ammonium methosulfate, di(stearoyloxyisopropyl) dimethyl quaternary ammonium chloride, di(oleoyloxybutyl) dimethyl quaternary ammonium chloride, di(oleoyloxyisopropyl) )
Dimethyl quaternary ammonium methosulfate, di(elaidioyloxyethyl)dimethyl quaternary ammonium chloride, (stearoyloxyethyl)(oleoyloxyethyl)dimethyl quaternary ammonium chloride,
(stearoyloxyisopropyl) (oleoyloxyisopropyl) dimethyl quaternary ammonium methosulfate, (palmitoyloxyethyl) (oleoyloxyethyl) dimethyl quaternary ammonium chloride, (
Examples include (stearoyloxyisopropyl) (elaidioyloxyisopropyl) dimethyl quaternary ammonium methosulfate, (stearoyloxybutyl) (oleoyloxybutyl) dimethyl quaternary ammonium chloride, and when one of these is used alone, You may also use a mixture of two or more types.

【0014】また、上記(I)式の第4級アンモニウム
塩は、例えば高級脂肪酸又は高級脂肪酸エステルと相応
する(ポリオキシアルキレン)アルカノールアミンとを
エステル化又はエステル交換した後、4級化の反応を進
めるなどして通常の方法で製造することができるが、R
1及びR2の総アルキル基の飽和アルキル基/不飽和ア
ルキル基の割合を上記特定重量比率とする方法としては
、上記製造方法において高級脂肪酸又は高級脂肪酸エス
テルを予め特定重量比率となるように混合して反応に供
する方法が好適に採用されるが、組成物を調製する際に
(I)式の化合物の2種類以上を混合して上述したよう
にアルキル基を上記特定重量比率の範囲に調整してもよ
い。
Further, the quaternary ammonium salt of the above formula (I) can be prepared by, for example, esterifying or transesterifying a higher fatty acid or a higher fatty acid ester with a corresponding (polyoxyalkylene) alkanolamine, and then subjecting it to a quaternization reaction. Although R
As a method for adjusting the ratio of saturated alkyl groups/unsaturated alkyl groups of the total alkyl groups of 1 and R2 to the above specific weight ratio, in the above production method, higher fatty acids or higher fatty acid esters are mixed in advance to a specific weight ratio. However, when preparing the composition, two or more types of compounds of formula (I) are mixed and the alkyl groups are adjusted to the above-mentioned specific weight ratio range as described above. You can.

【0015】(I)式の第4級アンモニウム塩の配合量
は、組成物全体の0.5〜30%(重量%、以下同様)
、特に3〜20%とすることが好ましく、配合量が0.
5%に満たないと柔軟性付与効果に劣る場合があり、3
0%を超えると柔軟剤組成物がゲル化して均一な組成物
にならない場合がある。
[0015] The amount of the quaternary ammonium salt of formula (I) is 0.5 to 30% (weight%, the same applies hereinafter) of the entire composition.
In particular, it is preferably 3 to 20%, and the blending amount is 0.
If it is less than 5%, the flexibility imparting effect may be inferior;
If it exceeds 0%, the softener composition may gel and may not be a uniform composition.

【0016】更に、本発明組成物はpHが1〜5、特に
2〜4であることが好ましく、このため、必要に応じて
pHの調整剤として通常用いられている有機又は無機の
酸又はアルカリ性化合物などを使用してpHを調整する
ことが好ましい。pH調整剤としては、例えば塩酸、硫
酸、アルカリ金属水酸化物、アルカリ金属炭酸塩、アル
カリ金属珪酸塩などの無機化合物、リン酸、多価カルボ
ン酸、高分子カルボン酸、高分子アクリル酸、有機アミ
ン化合物等の有機化合物などが挙げられる。
Furthermore, it is preferable that the composition of the present invention has a pH of 1 to 5, particularly 2 to 4. Therefore, if necessary, an organic or inorganic acid or alkaline acid which is commonly used as a pH adjuster may be used. It is preferable to adjust the pH using a compound or the like. Examples of pH adjusting agents include hydrochloric acid, sulfuric acid, inorganic compounds such as alkali metal hydroxides, alkali metal carbonates, and alkali metal silicates, phosphoric acid, polycarboxylic acids, polymer carboxylic acids, polymer acrylic acids, and organic compounds. Examples include organic compounds such as amine compounds.

【0017】本発明の液体柔軟剤組成物には上記必須成
分以外にその他の任意成分として、通常柔軟剤組成物に
配合される公知の成分を本発明の効果を妨げない範囲で
配合することができる。任意成分としては、例えば上記
(I)式の第4級アンモニウム塩以外の公知の柔軟剤基
剤(例えばジ長鎖アルキルジ短鎖アルキル第4級アンモ
ニウム塩等)、ステアリン酸、オレイン酸等の高級脂肪
酸、ステアリルアルコールのエチレンオキシド付加物、
牛脂アミンのエチレンオキシド付加物、ステアリルモノ
エタノールアミドのエチレンオキシド付加物、オクチル
フェノールのエチレンオキシド付加物、牛脂脂肪酸のエ
チレンオキシド付加物、オレイルアルコールのエチレン
オキシド付加物、オレイルアミンのエチレンオキシド付
加物の炭素数11〜22のアルコール、アミン、アルカ
ノールアミド及び脂肪酸から選ばれる化合物にアルキレ
ンオキシドが平均付加モル数30〜150において付加
したノニオン界面活性剤(このノニオン界面活性剤の配
合量は組成物全体の0.05〜30%、特に0.1〜2
0%とすることが好ましい)、2−エチルヘキサン酸と
グリセリン又はペンタエリストールとの部分エステル化
物等のノニオン界面活性剤などの界面活性剤、食塩、塩
化アンモニウム、塩化カルシウム等の水溶性塩、エチル
アルコール、イソプロピルアルコール、プロピレングリ
コール、エチレングリコール等の溶剤、尿素、殺菌剤、
酸化防止剤、顔料、染料、シリコーン類、炭化水素、セ
ルロース誘導体、紫外線吸収剤、蛍光増白剤、香料等が
挙げられる。なお、これら任意成分の配合量は本発明の
効果を妨げない範囲で通常量とすることができる。
[0017] In addition to the above-mentioned essential components, the liquid softener composition of the present invention may contain other optional components, such as known components that are usually incorporated into softener compositions, within the range that does not impede the effects of the present invention. can. Optional components include, for example, known softener bases other than the quaternary ammonium salt of the above formula (I) (for example, di-long-chain alkyl di-short-chain alkyl quaternary ammonium salts, etc.), higher-grade softeners such as stearic acid, oleic acid, etc. fatty acids, ethylene oxide adducts of stearyl alcohol,
Ethylene oxide adduct of beef tallow amine, ethylene oxide adduct of stearyl monoethanolamide, ethylene oxide adduct of octylphenol, ethylene oxide adduct of beef tallow fatty acid, ethylene oxide adduct of oleyl alcohol, alcohol having 11 to 22 carbon atoms of ethylene oxide adduct of oleylamine, A nonionic surfactant in which an alkylene oxide is added to a compound selected from amines, alkanolamides, and fatty acids at an average addition mole number of 30 to 150 (the amount of this nonionic surfactant is 0.05 to 30% of the entire composition, especially 0.1~2
(preferably 0%), surfactants such as nonionic surfactants such as partial esters of 2-ethylhexanoic acid and glycerin or pentaerythtol, water-soluble salts such as common salt, ammonium chloride, calcium chloride, etc. Solvents such as ethyl alcohol, isopropyl alcohol, propylene glycol, ethylene glycol, urea, disinfectants,
Antioxidants, pigments, dyes, silicones, hydrocarbons, cellulose derivatives, ultraviolet absorbers, optical brighteners, fragrances and the like can be mentioned. The amounts of these optional components can be set to normal amounts within a range that does not impede the effects of the present invention.

【0018】[0018]

【発明の効果】本発明の液体柔軟剤組成物は、良好な柔
軟性及び帯電防止性付与効果を有する上、吸水性保持効
果に優れ、しかも、生分解性に優れており環境汚染の問
題がほとんどない。従って、本発明組成物は、各種衣料
に幅広く利用することができる。
Effects of the Invention The liquid softener composition of the present invention not only has good flexibility and antistatic properties, but also has an excellent water absorbency retention effect, and is also excellent in biodegradability, so there is no problem of environmental pollution. rare. Therefore, the composition of the present invention can be widely used in various types of clothing.

【0019】[0019]

【実施例】以下、実施例及び比較例を示して本発明を具
体的に説明するが、本発明は下記実施例に制限されるも
のではない。なお、各例中の%はいずれも重量%である
[Examples] The present invention will be specifically explained below with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples. In addition, all % in each example is weight %.

【0020】また、各例の評価は下記の方法で行った。 柔軟性、帯電防止性、吸水性の評価: (1)仕上げ処理方法 市販の綿タオル、綿メリヤス布及びアクリル布を市販衣
料用洗剤「ハイトップ」(商品名、ライオン(株)製)
により電気洗濯機を用いて50℃で2回繰り返し洗濯後
、常温の水道水で充分すすぎ、これを試験布とした。
[0020]Each example was evaluated by the following method. Evaluation of flexibility, antistatic property, and water absorption: (1) Finishing method Commercially available cotton towels, cotton knitted cloth, and acrylic cloth were treated with commercially available laundry detergent "Hi-Top" (trade name, manufactured by Lion Corporation).
After washing the cloth twice at 50° C. using an electric washing machine, the cloth was thoroughly rinsed with tap water at room temperature, and this was used as a test cloth.

【0021】次に、25℃の水道水30リットルに対し
柔軟剤組成物を第4級アンモニウム塩の添加量として1
gになるように加えて均一溶液とした。この溶液中に浴
比30倍で各試験布を浸して3分間処理した後、2分間
脱水した。このように処理した布を風乾した後、柔軟性
及び吸水性評価用の綿タオルと綿メリヤス布は25℃、
65%RHの条件で24時間放置し、また、帯電防止性
評価用のアクリル布は20℃、55%RHの条件で72
時間放置し、それぞれの評価試験に用いた。 (2)柔軟性評価方法 表1に示すジメチルジ硬化牛脂アンモニウムクロライド
を柔軟剤基剤として配合した柔軟剤組成物(比較例)で
処理した布を対照にして一対比較を行い、下記基準にて
評価した。 +2:対照より柔らかい +1:対照よりやや柔らかい 0:対照と同じ −1:対照のほうがやや柔らかい −2:対照のほうが柔らかい (3)帯電防止性評価方法 スタチックネオストメーター(宍戸商会製)を用い、印
加電圧7KV、タ−ゲット距離20mmでアクリル布を
帯電させ、電圧除去後の半減期(秒)を測定した。 (4)吸水性評価方法 JIS  L  1096〜1979に準じ、2cm×
15cmの綿メリヤス布をインクで着色した純水(25
℃)に5mm浸漬し、5分間に上昇する水の高さを測定
した。
Next, the softener composition was added to 30 liters of tap water at 25°C as the amount of quaternary ammonium salt added.
g to make a homogeneous solution. Each test cloth was immersed in this solution at a bath ratio of 30 times, treated for 3 minutes, and then dehydrated for 2 minutes. After air-drying the fabrics treated in this way, the cotton towels and cotton knitted fabrics for softness and water absorption evaluation were heated at 25°C.
The acrylic cloth for antistatic evaluation was left at 20°C and 55% RH for 24 hours.
It was left to stand for a period of time and used for each evaluation test. (2) Softness evaluation method A pairwise comparison was made using a fabric treated with a fabric softener composition (comparative example) containing dimethyldicured beef tallow ammonium chloride as a fabric softener base shown in Table 1, and evaluated using the following criteria. did. +2: Softer than the control +1: Slightly softer than the control 0: Same as the control -1: Slightly softer than the control -2: Softer than the control (3) Antistatic property evaluation method Using a static neostometer (manufactured by Shishido Shokai) The acrylic cloth was charged with an applied voltage of 7 KV and a target distance of 20 mm, and the half-life (seconds) after the voltage was removed was measured. (4) Water absorbency evaluation method according to JIS L 1096-1979, 2cm x
Pure water (25cm) colored with ink on a 15cm cotton knitted cloth
℃), and the height of water rising in 5 minutes was measured.

【0022】〔実施例1,2、比較例〕表1に示す柔軟
剤水性分散組成物を調製し、上記方法で柔軟性、帯電防
止性、吸水性を評価した。結果を表1に併記する。
[Examples 1 and 2, Comparative Example] Aqueous softener dispersion compositions shown in Table 1 were prepared, and their flexibility, antistatic properties, and water absorption properties were evaluated using the methods described above. The results are also listed in Table 1.

【0023】[0023]

【表1】[Table 1]

【0024】表1の結果より、本発明の液体柔軟剤組成
物(実施例1,2)は、柔軟性及び帯電防止性付与効果
に優れている上、吸水性付与効果に優れることが確認さ
れた。また、生分解性も良好であった。
From the results in Table 1, it was confirmed that the liquid softener compositions of the present invention (Examples 1 and 2) are excellent in imparting flexibility and antistatic properties, and are also excellent in imparting water absorption properties. Ta. Moreover, the biodegradability was also good.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】  下記一般式(I)で示される第4級ア
ンモニウム塩を含有してなることを特徴とする液体柔軟
剤組成物。 【化1】 〔但し、式中R1、R2はそれぞれ炭素数11〜23の
飽和又は不飽和アルキル基で、かつ、R1及びR2の総
アルキル基は飽和アルキル基:不飽和アルキル基(重量
比)が2:98〜30:70の範囲である。また、R3
、R4はそれぞれ炭素数1〜4のアルキル基又はヒドロ
キシアルキル基、R5、R6はそれぞれCmH2m(但
し、m=2〜4)であり、X−は陰イオン、nは1〜4
の数である。〕
1. A liquid softener composition comprising a quaternary ammonium salt represented by the following general formula (I). [Formula 1] [However, in the formula, R1 and R2 are each a saturated or unsaturated alkyl group having 11 to 23 carbon atoms, and the total alkyl group of R1 and R2 is saturated alkyl group: unsaturated alkyl group (weight ratio) is in the range of 2:98 to 30:70. Also, R3
, R4 are each an alkyl group or hydroxyalkyl group having 1 to 4 carbon atoms, R5 and R6 are each CmH2m (however, m = 2 to 4), X- is an anion, and n is 1 to 4
is the number of ]
JP13551591A 1991-05-10 1991-05-10 Liquid softener composition Expired - Lifetime JP2956274B2 (en)

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Application Number Priority Date Filing Date Title
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JPH04333667A true JPH04333667A (en) 1992-11-20
JP2956274B2 JP2956274B2 (en) 1999-10-04

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995016766A1 (en) * 1993-12-13 1995-06-22 The Procter & Gamble Company Viscosity stable concentrated liquid fabric softener compositions
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
US5505866A (en) * 1994-10-07 1996-04-09 The Procter & Gamble Company Solid particulate fabric softener composition containing biodegradable cationic ester fabric softener active and acidic pH modifier
US5545340A (en) * 1993-03-01 1996-08-13 The Procter & Gamble Company Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains
US6083899A (en) * 1996-09-19 2000-07-04 The Procter & Gamble Company Fabric softeners having increased performance
US6369025B1 (en) 1995-07-11 2002-04-09 The Procter & Gamble Company Concentrated, water dispersible, stable, fabric softening compositions
JP2013534516A (en) * 2010-06-02 2013-09-05 エヴォニク ゴールドシュミット ゲーエムベーハー Quaternary dialkanolamine esters

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5545340A (en) * 1993-03-01 1996-08-13 The Procter & Gamble Company Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains
US5562849A (en) * 1993-03-01 1996-10-08 The Procter & Gamble Company Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains
US5574179A (en) * 1993-03-01 1996-11-12 The Procter & Gamble Company Concentrated biodegradable quaternary ammonium fabric softener compositions and compouds containing intermediate iodine value unsaturated fatty acid chains
WO1995016766A1 (en) * 1993-12-13 1995-06-22 The Procter & Gamble Company Viscosity stable concentrated liquid fabric softener compositions
US5505866A (en) * 1994-10-07 1996-04-09 The Procter & Gamble Company Solid particulate fabric softener composition containing biodegradable cationic ester fabric softener active and acidic pH modifier
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
US6369025B1 (en) 1995-07-11 2002-04-09 The Procter & Gamble Company Concentrated, water dispersible, stable, fabric softening compositions
US6083899A (en) * 1996-09-19 2000-07-04 The Procter & Gamble Company Fabric softeners having increased performance
JP2013534516A (en) * 2010-06-02 2013-09-05 エヴォニク ゴールドシュミット ゲーエムベーハー Quaternary dialkanolamine esters
US9073818B2 (en) 2010-06-02 2015-07-07 Evonik Degussa Gmbh Quaternary dialkanolamine esters

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