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JPS5946560B2 - Detergent composition that gives flexibility to clothing - Google Patents
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JPS5946560B2 - Detergent composition that gives flexibility to clothing - Google Patents

Detergent composition that gives flexibility to clothing

Info

Publication number
JPS5946560B2
JPS5946560B2 JP6524079A JP6524079A JPS5946560B2 JP S5946560 B2 JPS5946560 B2 JP S5946560B2 JP 6524079 A JP6524079 A JP 6524079A JP 6524079 A JP6524079 A JP 6524079A JP S5946560 B2 JPS5946560 B2 JP S5946560B2
Authority
JP
Japan
Prior art keywords
weight
detergent composition
detergent
foaming
clothing
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.)
Expired
Application number
JP6524079A
Other languages
Japanese (ja)
Other versions
JPS55160097A (en
Inventor
武信 阪谷
滋 鈴木
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 JP6524079A priority Critical patent/JPS5946560B2/en
Publication of JPS55160097A publication Critical patent/JPS55160097A/en
Publication of JPS5946560B2 publication Critical patent/JPS5946560B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は衣類の洗浄を行なうと同時に良好な風合い、柔
軟性を与える洗剤組成物に関するもので、さらに詳しく
は洗濯中での豊かな泡立ち及び洗浄力を損なわずに衣類
を柔軟に仕上げる洗剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a detergent composition that not only cleans clothes but also gives them a good texture and softness. This invention relates to a detergent composition that gives a soft finish.

従来の衣類用の重質洗剤を用いて衣類、例えば綿肌着や
おむつ等を洗つた場合、仕上り感がゴワゴワし、ふつく
らした感じがないし、又合成繊維布を洗つた場合は柔ら
かさやスベスベしたスリップ性が不十分なものである。
When washing clothes, such as cotton underwear or diapers, using conventional heavy detergents for clothes, the finish feels stiff and fluffy, and when washing synthetic fiber cloth, it does not feel soft or smooth. The slip property is insufficient.

この為、洗浄した衣類に良好な風合いを与えたり、柔軟
性を与えるために、すすぎ後にジ長鎖アルキルジメチル
アンモニウム等のカチオン界面活性剤を主成分とする柔
軟仕上剤を使用する事が良く行なわれている。衣類用重
質洗剤は通常アニオン界面活性剤を主成分としていろの
で柔軟剤がカチオン界面活性剤を主成分とする場合は、
柔軟仕上剤を洗浄中にそのまま使用する事は好ましくな
い。柔軟仕上剤中のカチオン界面活性剤と反応して水不
溶物を生じるばかりでなく、柔軟効果、洗浄力ないしは
起泡力が著しく損なわれるからである。これに対してア
ニオン活性剤と反応しないアニオン界面活性剤、ノニオ
ン界面活性剤、両性界面活性剤ないしは油性成分を洗剤
成分に添加し、洗濯時に良好な風合いを付与させること
を意図した洗剤組成物もいくつか提案されている。
For this reason, in order to give washed clothes a good texture and flexibility, it is common practice to use a fabric softener containing a cationic surfactant such as di-long-chain alkyldimethylammonium as a main ingredient after rinsing. It is. Heavy laundry detergents usually have anionic surfactants as their main ingredient, so if your fabric softener has a cationic surfactant as its main ingredient,
It is not recommended to use fabric softener directly during washing. This is because not only does it react with the cationic surfactant in the softener to produce water-insoluble substances, but also the softening effect, detergency or foaming power is significantly impaired. On the other hand, there are also detergent compositions in which an anionic surfactant, a nonionic surfactant, an amphoteric surfactant, or an oily component that does not react with the anionic surfactant is added to the detergent component to impart a good texture during washing. Some suggestions have been made.

例えば特定の石鹸化合物の添加(米国特許第36259
05号、米国特許第1329416号)、長鎖ヒドロキ
シエーテルスルホン酸塩や分子内環状サルトンの添加(
米国特許第3627822号、米国特許第407145
6号)等の方法が知られているが、これらの物質はいず
れも添加量がかなり多くないと十分な効果が得られない
し、また洗濯中で起泡件を損なラ事もあり好ましくない
。泡立ちの低下は必らずしも洗浄力の低下を意味するも
のでないが、一般の消費者は泡立ちの良否を洗浄剤性能
の優劣を決める判断基準とする傾向があるため、泡立ち
の低下は商品価値上大きな問題となる。本発明者等は洗
濯と同時に衣類に柔軟効果を付辱し、しかも洗濯時にお
いて泡立ちの低下しない洗浄剤組成物を得るため、鋭意
研究を行なつた結果、特定の炭素鎖長を有する比較的高
分子量のαオレフインスルホン酸塩と水難溶性のジ長鎖
アルキル4級アンモニウム塩とを併用することにより比
較的少量の添加で、目的を達する事ができることを見出
し、この知見に基づいて本願発明を完成するに至つた。
即ち本発明は、 (a)炭素数20〜24の範囲で、炭素数22の割合が
少なくとも35重量%であるα−オレフインスルホン酸
塩2〜10重量%、(b) 一般式 (ここでR1及びR2は10〜22の平均炭素数を有す
るアルキル基又はアルケニル基、R3及びR4は1〜3
の炭素数を有するアルキル基、Xはハロゲン原子を示す
)で表わされるカチオン活性剤0.3〜3重量%、(c
)洗剤活性を有するアニオン活性剤及び/又はノニオン
活性剤1〜30重量%、を含むことを特徴とする洗剤組
成物であつて、これにより所期の目的を達成したのであ
る。
For example, the addition of certain soap compounds (US Pat. No. 36,259)
No. 05, U.S. Pat.
U.S. Patent No. 3,627,822, U.S. Patent No. 4,07145
Methods such as No. 6) are known, but these substances are undesirable because they do not have sufficient effect unless they are added in a fairly large amount, and they also impair foaming properties during washing. . Although a decrease in foaming does not necessarily mean a decrease in cleaning power, general consumers tend to use the quality of foaming as a criterion for determining the performance of detergents. This is a big problem in terms of value. The present inventors conducted intensive research in order to obtain a detergent composition that imparts a softening effect to clothing at the same time as washing and does not reduce foaming during washing. It was discovered that by using a high molecular weight α-olefin sulfonate and a sparingly water-soluble di-long chain alkyl quaternary ammonium salt, the objective could be achieved with a relatively small amount of addition, and based on this knowledge, the present invention was developed. It was completed.
That is, the present invention provides (a) 2 to 10% by weight of an α-olefin sulfonate having a carbon number of 20 to 24 and a proportion of 22 carbons of at least 35% by weight, (b) a general formula (wherein R1 and R2 is an alkyl group or alkenyl group having an average carbon number of 10 to 22, R3 and R4 are 1 to 3
0.3 to 3% by weight of a cationic activator represented by an alkyl group having a carbon number of
) A detergent composition characterized by containing 1 to 30% by weight of an anionic activator and/or a nonionic activator having detergent activity, thereby achieving the intended purpose.

本発明に使用するα−オレフインスルホン酸塩は、ワツ
クスクラツキング法、チーグラ一触媒によるエチレン重
合法又はそれらの改良法で得られた炭素数20〜24の
範囲の混合α−オレフインを薄膜状とし、不活性ガスで
希釈したガス状無水硫酸でスルホン化したのち、水酸化
ナトリウム又は水酸化カリウムで中和し、次いで加水分
解して得ることができる。
The α-olefin sulfonate used in the present invention is a thin film of a mixed α-olefin with a carbon number ranging from 20 to 24 obtained by the wax cracking method, the ethylene polymerization method using a Ziegler catalyst, or an improved method thereof. It can be obtained by sulfonating with gaseous anhydrous sulfuric acid diluted with an inert gas, neutralizing with sodium hydroxide or potassium hydroxide, and then hydrolyzing.

このようにして得られたα−オレフインスルホン酸塩に
はモノスルホン酸塩とジスルホン酸塩が含まれ、前者の
中にはさらにアルケンスルホン酸塩とヒドロキシアルカ
ンスルホン酸塩とが存在する。
The α-olefin sulfonate thus obtained contains monosulfonate and disulfonate, and the former further includes alkene sulfonate and hydroxyalkane sulfonate.

アルケンスルホン酸塩とヒドロキシアルカンスルホン酸
塩の比率は40:60ないし90:10、好ましくは5
0:50ないし80:20である。本発明においては、
前記のα−オレフインスルホン酸塩についてその中の炭
素鎖長22のものが、全体の35%以上を占めるように
調整することにより優れた衣類柔軟化効果を示す。配合
量は全量の2〜10重量%で3〜5重量%が好ましい。
2%未満では柔軟効果が十分でなく、10%を越えると
泡立ちが低下する。
The ratio of alkenesulfonate to hydroxyalkanesulfonate is 40:60 to 90:10, preferably 5
The time is from 0:50 to 80:20. In the present invention,
By adjusting the above α-olefin sulfonate so that those having a carbon chain length of 22 account for 35% or more of the total, an excellent clothing softening effect is exhibited. The blending amount is 2 to 10% by weight, preferably 3 to 5% by weight of the total amount.
If it is less than 2%, the softening effect will not be sufficient, and if it exceeds 10%, foaming will be reduced.

このもの自体は泡立ちが殆んど無い。次に第4級アンモ
ニウム塩としてはジアルキルタイプ、モノアルキルトリ
メチルタイプ、モノアルキルベンジルジメチルタイプが
知られているが、本発明ではジアルキルタイプが好まし
い。
This product itself has almost no foaming. Next, dialkyl type, monoalkyltrimethyl type, and monoalkylbenzyldimethyl type are known as quaternary ammonium salts, but dialkyl type is preferred in the present invention.

その他のタイプでは柔軟効果が十分でない。その具体例
としてはジステアリルジメチルアンモニウム塩、ジ硬化
牛脂アルキルジメチルアンモニウム塩、ジ硬化牛脂アル
キルベンジルメチルアンモニウム塩、ジステアリルメチ
ルベンジルアンモニウム塩、ジステアリルメチルヒドロ
キシエチルアンモニウム塩、ジステアリルメチルヒドロ
キシプロピルアンモニウム塩、ジステアリルジヒドロキ
シエチルアンモニウム塩等で対イオンがクロリド又はプ
ロミドが挙げられる。配合量は全量の0.3〜3重量%
で0.5〜1.5重量%が好ましく、0.3%未満では
柔軟効果が十分でなく、3%を越えると泡立ちは低下し
、又、洗浄力も劣化する傾向がある。使用する第4級ア
ンモニウム塩の形態は平均粒径50μ〜250μの造粒
物が好ましい。造粒物は第4級アンモニウム塩のみでも
よいが、この場合は粉粒状洗剤として貯蔵中に温度等に
より軟化熔融して、粉粒状洗剤を固化させる原因ともな
るのでトリポリ燐酸ソーダ等の洗剤ビルダ一粉末といつ
しよにスプレー乾燥したものや、溶融混合後冷却固化さ
せて造粒した物が良い。更に洗剤活性を有するアニオン
界面活性剤及び/又はノニオン界面活性剤としては、(
a)アルキルベンゼンスルホン酸塩; 平均炭素数が9〜15個のアルキル基を持つアルキルベ
ンゼンのスルホン化物(b) α−オレフインスルホン
酸塩; ワツクスクラツキング法、チーグラ一触媒によるエチレ
ン重合法又はこれらの改良法で得られたClO−C2O
のα−オレフインを原料とし、公知の方法でスルホン化
反応後、アルカリで中和し、次いで加水分解して得られ
る。
Other types do not have sufficient flexibility. Specific examples include distearyldimethylammonium salt, dicured tallow alkyldimethylammonium salt, dicured tallow alkylbenzylmethylammonium salt, distearylmethylbenzylammonium salt, distearylmethylhydroxyethylammonium salt, and distearylmethylhydroxypropylammonium salt. , distearyl dihydroxyethylammonium salt, etc., with the counter ion being chloride or bromide. The blending amount is 0.3 to 3% by weight of the total amount.
The amount is preferably from 0.5 to 1.5% by weight; if it is less than 0.3%, the softening effect will not be sufficient, and if it exceeds 3%, foaming will decrease and detergency will also tend to deteriorate. The quaternary ammonium salt used is preferably in the form of granules with an average particle size of 50 μm to 250 μm. The granules may be made of only quaternary ammonium salts, but in this case, detergent builders such as sodium tripolyphosphate may be used as powdered detergents, as they may soften and melt due to temperature during storage, causing the powdery detergents to solidify. It is best to use a powder that has been spray-dried, or one that has been melt-mixed, cooled and solidified, and then granulated. Further, as anionic surfactants and/or nonionic surfactants having detergent activity, (
a) Alkylbenzene sulfonate; Sulfonated product of alkylbenzene having an alkyl group having an average carbon number of 9 to 15 (b) α-olefin sulfonate; Wax scratching method, ethylene polymerization method using a Ziegler catalyst, or these ClO-C2O obtained by improved method
It is obtained by using α-olefin as a raw material, after sulfonation reaction by a known method, neutralization with an alkali, and then hydrolysis.

(c)アルキルサルフエート; 平均炭素数が8〜20個の高級アルコールの硫酸化物(
第2級、不飽和、分枝鎖があつても良い)(d)アルキ
ルエーテルサルフエート; 平均炭素数が10〜18個の高級アルコールにエチレン
オキシドを平均1〜10個付加した後硫酸化(第2級、
不飽和、分枝鎖があつても良い)(e)アルカンスルホ
ネート: 平均炭素数が10〜20個のn−パラフインをスルホキ
シデーシヨンしてアルカンスルホン酸とした後中和する
(c) Alkyl sulfate; sulfate of higher alcohol having an average carbon number of 8 to 20 (
Secondary, unsaturated, branched chain may be present) (d) Alkyl ether sulfate; After adding 1 to 10 ethylene oxides on average to a higher alcohol having an average number of carbon atoms of 10 to 18, sulfation 2nd class,
(e) Alkanesulfonate: N-paraffin having an average carbon number of 10 to 20 is sulfoxidized to form an alkanesulfonic acid, and then neutralized.

(f)α−スルホ脂肪酸エステル: 平均炭素数が10〜20個の脂肪酸のメチル又はエチル
エステルをスルホン化した物。
(f) α-Sulfo fatty acid ester: A sulfonated methyl or ethyl ester of a fatty acid having an average carbon number of 10 to 20.

(支) アルコールエトキシレート; アルキル基炭素数8〜15、EOP−5〜(h)アルキ
ルアリルエトキシレート; アルキル基炭素数7〜15、EOP−5〜などが挙げら
れ、その使用量は全量の1〜30重量%である。
(Support) Alcohol ethoxylate; Alkyl group having 8 to 15 carbon atoms, EOP-5 to (h) Alkylaryl ethoxylate; Alkyl group having 7 to 15 carbon atoms, EOP-5 to It is 1 to 30% by weight.

以上は本発明の必須成分であるが、ビルダ一類やキレー
ト剤等の任意成分が併用される。
The above are essential components of the present invention, but optional components such as builders and chelating agents are used in combination.

そして任意成分としては珪酸ナトリウム、炭酸ナトリウ
ム、トリポリ燐酸ナトリウム、ピロ燐酸ナトリウム、オ
ルソ燐酸ナトリウム、アルミノシリケート等の無機ビル
ダ一、ポリカルボン酸塩(例えば無水マレイン酸、アク
リル酸の重合体、もしくはオレフインとの共重合物)、
ニトリロトリ酢酸ナトリウム(NTA)クエン酸ナトリ
ウム等の有機ビルダ一、EDTA等の有機キレート剤、
カルボキシルメチルセルロース(CMC)等の再汚染防
止剤、石鹸等の濯ぎ改良剤アンチケーキング剤、螢光増
白剤、香料等が挙げられる。実施例 1(実験洗1〜9
) 下記組成で9通りの組成物を作りその柔軟性、洗浄力、
泡立ちを測定しその結果を表−1に示す。
Optional ingredients include inorganic builders such as sodium silicate, sodium carbonate, sodium tripolyphosphate, sodium pyrophosphate, sodium orthophosphate, aluminosilicate, polycarboxylic acid salts (for example, maleic anhydride, acrylic acid polymers, or olefins) copolymer),
Organic builders such as sodium nitrilotriacetate (NTA) and sodium citrate, organic chelating agents such as EDTA,
Examples include anti-restaining agents such as carboxymethyl cellulose (CMC), rinsing improvers such as soaps, anti-caking agents, fluorescent whitening agents, fragrances and the like. Example 1 (Experimental washing 1-9
) Nine compositions were made with the following compositions, and their flexibility, detergency,
Foaming was measured and the results are shown in Table 1.

但し洗浄力、柔軟性(風合い)及び泡立ち性は以下の試
験法によつた。洗浄力試1験 試布(60番綿プロード)をワイシヤツの衿に装着し、
2〜5日間着用して汚染後、取りはずしたもの及び、別
に2〜3日間着用した肌シヤツ(綿メリヤス)を用意す
る。
However, the detergency, flexibility (texture) and foaming properties were determined by the following test methods. Cleaning power test 1 Attach the test cloth (No. 60 cotton prod) to the collar of the dress shirt,
Prepare one that has been worn for 2 to 5 days and removed after becoming contaminated, and a skin shirt (cotton knitted) that has been worn for another 2 to 3 days.

このように汚染された試布20枚と肌シヤツ及び清浄綿
タオルを噴流式家庭用電気洗濯機を用いて洗剤濃度0.
133%、液温25℃、浴比30倍で10分間洗濯した
後、3分間づつ2回すすぐ。
Twenty sample cloths contaminated in this way, a skin shirt, and a clean cotton towel were washed with a detergent concentration of 0 using a jet-type household electric washing machine.
133%, liquid temperature 25°C, bath ratio 30 times for 10 minutes, and then rinsed twice for 3 minutes each.

洗浄効率は洗浄前後の汚垢布の反射率を走査型光電反射
率計を用いて測定し次式より求める。からなる試験布を
用いて、洗浄力試験の条件で洗濯、すすぎ後、1分間脱
水後試験布を24時間風乾し、次に25℃、65%RH
の条件下に風乾試験布をコンデイシヨニングした。こう
して得られた試験布のなかからナイロントリコツト布を
取り出し、判定者を10名選び、感触により判定した。
The cleaning efficiency is determined from the following formula by measuring the reflectance of the dirty cloth before and after cleaning using a scanning photoelectric reflectance meter. Using a test cloth made of
The air-dried test fabric was conditioned under the following conditions. A nylon tricot cloth was taken out of the test cloths thus obtained, and 10 judges were selected and judged based on feel.

判定は市販洗剤(ライオン油脂(株)製品スパーク)で
洗浄後、市販柔軟仕土剤(ライオン油脂(株)製品ソフ
ランS)で処理したものを2点とし、市販洗剤のみで洗
濯したものをO点とし、その中間を1点とし、10名の
合計点で行なつた。
Items washed with a commercially available detergent (Lion Yushi Co., Ltd. product Spark) and then treated with a commercially available soil softener (Lion Yushi Co., Ltd. product Soflan S) were given 2 points, and items washed only with a commercially available detergent were given O. The score was given as a point, and the middle point was taken as 1 point, and the total score of 10 people was used.

泡立ち試験洗浄力試験の条件で洗濯終了後に生成した泡
を水面全体にならし泡の高さを測定した。
Foaming Test Under the conditions of the detergency test, the foam generated after washing was leveled over the entire water surface and the height of the foam was measured.

土表の結果より、本発明の組成物(実験A6.l〜9)
は、比較例(実験/F6.lO〜17)に比べ、柔軟性
、洗浄力、泡立ち共すぐれていることが判る。
From the soil surface results, the composition of the present invention (Experiment A6.1-9)
It can be seen that compared to the comparative example (experiment/F6.1O~17), the softness, detergency, and foaming properties of the sample were superior.

実施例 2(実験A6.l8〜21)下記配合組成の組
合せでα−オレフインスルホン酸ソーダおよびカチオン
界面活性剤の種類の影響を検討した結果を表〜2に示す
Example 2 (Experiment A6.18-21) Tables 2 show the results of examining the influence of the types of α-olefin sulfonic acid sodium and cationic surfactant in the combinations of the following formulations.

注(1)カチオン活性剤/トリポリリン酸ソータZ硫酸
マグネシウム−25/35/40の45%スラリーをデ
イスク型スプレーで噴霧乾燥して得たもの 表−2の結果より、実施例は比較例に比べ、柔軟性、洗
浄力、泡立ち共すぐれていることが判る。
Note (1) Obtained by spray-drying a 45% slurry of cationic activator/tripolyphosphate sorter Z magnesium sulfate-25/35/40 with a disk type spray. From the results in Table 2, the Examples are compared to the Comparative Examples. It can be seen that it has excellent flexibility, detergency, and foaming properties.

実施例 3(実験7f6.26〜34)O下記配合組成
の組合ぜは、洗浄力、柔軟性、泡立ち共すぐれていた。
Example 3 (Experiment 7f6.26-34) The combination of the following formulations was excellent in detergency, flexibility, and foaming.

Claims (1)

【特許請求の範囲】 1 下記(a)(b)(c)を含む事を特徴とする洗剤
組成物。 (a)炭素数20〜24の範囲で、炭素数22の割合が
少なくとも35重量%であるα−オレフィンスルホン酸
塩2〜10重量%。(b)一般式 ▲数式、化学式、表等があります▼ (ここでR_1及びR_2は10〜22の平均炭素数を
有するアルキル基又はアルケニル基、R_3及びR_4
は1〜3の炭素数を有するアルキル基、Xはハロゲン原
子を示す)で表わされるカチオン活性剤0.3〜3重量
%。 (c)洗剤活性を有するアニオン活性剤及び/又はノニ
オン活性剤1〜30重量%。
[Scope of Claims] 1. A detergent composition characterized by containing the following (a), (b), and (c). (a) 2 to 10% by weight of α-olefin sulfonates having a carbon number ranging from 20 to 24, with the proportion of carbon 22 being at least 35% by weight; (b) General formula ▲ Numerical formula, chemical formula, table, etc. ▼ (Here, R_1 and R_2 are alkyl groups or alkenyl groups having an average number of carbon atoms of 10 to 22, R_3 and R_4
is an alkyl group having 1 to 3 carbon atoms, and X represents a halogen atom). (c) 1 to 30% by weight of an anionic and/or nonionic activator having detergent activity.
JP6524079A 1979-05-26 1979-05-26 Detergent composition that gives flexibility to clothing Expired JPS5946560B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6524079A JPS5946560B2 (en) 1979-05-26 1979-05-26 Detergent composition that gives flexibility to clothing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6524079A JPS5946560B2 (en) 1979-05-26 1979-05-26 Detergent composition that gives flexibility to clothing

Publications (2)

Publication Number Publication Date
JPS55160097A JPS55160097A (en) 1980-12-12
JPS5946560B2 true JPS5946560B2 (en) 1984-11-13

Family

ID=13281185

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6524079A Expired JPS5946560B2 (en) 1979-05-26 1979-05-26 Detergent composition that gives flexibility to clothing

Country Status (1)

Country Link
JP (1) JPS5946560B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62171356U (en) * 1986-04-21 1987-10-30
JPS63108840U (en) * 1986-12-31 1988-07-13

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62171356U (en) * 1986-04-21 1987-10-30
JPS63108840U (en) * 1986-12-31 1988-07-13

Also Published As

Publication number Publication date
JPS55160097A (en) 1980-12-12

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