JPH0560520B2 - - Google Patents

Info

Publication number
JPH0560520B2
JPH0560520B2 JP60144366A JP14436685A JPH0560520B2 JP H0560520 B2 JPH0560520 B2 JP H0560520B2 JP 60144366 A JP60144366 A JP 60144366A JP 14436685 A JP14436685 A JP 14436685A JP H0560520 B2 JPH0560520 B2 JP H0560520B2
Authority
JP
Japan
Prior art keywords
weight
acid
fatty acid
zeolite
salts
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 - Lifetime
Application number
JP60144366A
Other languages
Japanese (ja)
Other versions
JPS624797A (en
Inventor
Hideji Tagata
Fumio Sai
Moryasu Murata
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.)
Kao Corp
Original Assignee
Kao 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 Kao Corp filed Critical Kao Corp
Priority to JP14436685A priority Critical patent/JPS624797A/en
Publication of JPS624797A publication Critical patent/JPS624797A/en
Publication of JPH0560520B2 publication Critical patent/JPH0560520B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Detergent Compositions (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、洗濯時の再汚染防止性に優れた洗浄
剤組成物に関する。 〔従来の技術〕 近年の石油化学産業の発展に伴い、衣類に占め
る化学繊維が増えて来た。化学繊維のほとんどは
疏水性物質からできているため、油状のものに対
して、非常に親和性が高い。そのため、洗濯中に
取り除かれた汚れが静電気的引力等により再沈着
し、衣類の黒ずみの大きな原因となつている。 ところで、汚れの再汚染防止剤としては、木綿
用としてCMCが使用され、また化学繊維用とし
てPEG、PVAなどの水溶性ポリマーが有効であ
るとされている。 従来、洗剤ビルダーとして、ポリ燐酸が使用さ
れていたが、環境上の問題から、ゼオライトに代
替されている。 〔発明が解決しようとする問題点〕 しかし、このゼオライトは硬水軟化作用には優
れるものの、汚れの分散能や、緩衝能等の他のビ
ルダー性能は非常に乏しい。再汚染防止能につい
ても同様で、PEG、CMCを併用してもポリ燐酸
塩を使用した洗剤には及ばない。 〔問題点を解決するための手段〕 そこで、ゼオライトを用いた無燐洗剤において
良好な再汚染防止能をもつ洗浄剤を提供すべく鋭
意研究を重ねた結果、α−スルホ脂肪酸エステル
塩とプルロツク型コポリマーの併用系にPEG添
加すると、被洗布が綿布であつても、化学繊維で
あつても、優れた効果があることを見いだし、こ
の知見に基づいて、本発明を完成するに至つた。 即ち、本発明は下記4成分(a)、(b)、(c)及び(d) (a) 一般式(1) (但し、R1はC6〜C20のアルキル基、R2はC1
C4のアルキル基、Mはアルカリ金属又はアル
カリ土類金属を示す)で表わされるα−スルホ
脂肪酸エステル塩1〜35重量% (b) 一般式(2) (但し、m,pは5〜100の数、nは5〜200の
数を示す)で表わされるプルロニツク型コポリ
マー0.1〜20重量% (c) 平均分子量1000〜20000のポリエチレングリ
コール0.5〜20重量% (d) ゼオライト5〜35重量% を含有する洗浄剤組成物を提供するものである。 本発明組成物の(a)成分であるα−スルホ脂肪酸
エステル塩としては炭素原子数10〜20、有利には
12〜18の直鎖状飽和脂肪酸のエステルの誘導体及
び炭素原子数1〜3の飽和1価アルコール、有利
にはメタノール及びエタノールが挙げられる。天
然の硬化脂肪酸及び脂肪酸重合物から製造される
スルホ脂肪酸エステルのナトリウム塩、例えばス
テアリン酸メチルエステル、パルミチン酸エチル
エステル、水素添加パーム核脂肪酸メチルエステ
ル又は水素添加した獣脂脂肪酸メチルエステルの
α−スルホン酸ナトリウム塩を使用するのが有利
である。α−スルホ脂肪酸エステル塩は一般に従
属する量でα−スルホ脂肪酸二塩を含み、これは
工業的後処理、例えばH2O2での漂白又は中和に
際してエステル結合の加水分解により生じ得る。
この二塩は工業的生成物の場合5〜25重量%の量
で含まれるが、これにより生成物の作用効果が害
なわれることはない。従つて以下においてα−ス
ルホ脂肪酸エステル塩とは工業的な二塩含有生成
物を意味する。 (a)成分は、1〜35重量%配合されるが、好まし
くは5〜25重量%の範囲である。1重量%以下で
は十分な効果はなく、35重量%以上配合しても格
別の効果は得られない。 (b)成分のプルロニツク型コポリマーは前述の一
般式(2)で表わされ、m、pは5〜100の数、nは
5〜200の数であるが、好ましくはm、np共に10
〜80である。また分子量は900以上、特に1000〜
10000でエチレンオキサイド含量は20〜80重量%、
特に35〜55重量%のものがよい。 (b)成分は0.1〜20重量%の範囲で配合されるが、
好ましくは1〜10重量%の範囲である。0.1重量
%以下の配合では十分な効果が得られず、20重量
%以上配合しても格別の効果はない。 (c)成分であるポリエチレングリコールは平均分
子量が1000〜20000のものである。平均分子量
1000未満、又は20000以上のものでは水硬度が高
い際に、再汚染防止能が低下する。これを、洗剤
中に0.5〜20重量%配合するとよいが、望ましく
は1〜10重量%の範囲である。0.5重量%以下で
は特別の効果はなく、20重量%以上になると、そ
の効果の相乗作用が一定となる。 本発明組成物における(d)成分のゼオライトとし
ては、例えばA型、X型又は無定型合成ゼオライ
トとして市販されているものを用いることがで
き、その含有量は5〜35重量%、好ましくは10〜
20重量%の範囲である。このゼオライトの含有量
が5重量%未満では製造時における粉体物性が劣
り、その上満足しうる洗浄力が得られず、また35
重量%を超えると被洗物にゼオライト粒子が付着
して好ましくない。 本発明の洗浄剤組成物には下記の各種界面活性
剤を併用することができる。 陰イオン界面活性剤としては、直鎖又は分岐鎖
アルキルベンゼンスルホン酸塩、アルキル又はア
ルケニルエーテル硫酸塩、アルキル又はアルケニ
ル硫酸塩、オレフインスルホン酸塩、アルカンス
ルホン酸塩、飽和又は不飽和脂肪酸塩、アルキル
又はアルケニルエーテルカルボン酸塩、アミノ酸
型界面活性剤、N−アシルアミノ酸型界面活性
剤、アルキル又はアルケニル燐酸エステル又はそ
の塩などが例示される。 陰イオン界面活性剤は、本発明の必須成分であ
る(a)成分を含めて一般の洗浄剤組成物における配
合量、即ち15〜35重量%とするのがよい。 両性界面活性剤としては、カルボキシ又はスル
ホベタイン型界面活性剤など、 非イオン界面活性剤としては、ポリオキシアル
キレンアルキル又はアルケニルエーテル、ポリオ
キシエチレンアルキルフエニルエーテル、高級脂
肪酸アルカノールアミド又はそのアルキレンオキ
サイド付加物、蔗糖脂肪酸エステル、脂肪酸エス
テル、脂肪酸グリセリンモノエステル、アルキル
アミンオキサイドなど、 カチオン性界面活性剤としては、第4級アンモ
ニウム塩などが例示される。 その他本発明の組成物には慣用の補助添加剤、
例えばトリポリ燐酸塩、ピロ燐酸塩等の燐酸塩、
エタン−1,1−ジホスホン酸の塩、2−ホスホ
ノブタン−1,2−ジカルボン酸等のホスホノカ
ルボン酸の塩、アスパラギン酸、グルタミン酸等
のアミノ酸の塩、ニトリロ3酢酸塩、エチレンジ
アミ4酢酸塩等のアミノポリ酢酸塩、ポリアクリ
ル酸、ポリアコニツト酸等の高分子電解質、ポリ
ビニルアルコール、ポリビニルピロリドン等の非
解離高分子、ジグリコール酸、オリシカルボン酸
塩などの有機酸の塩などの二価金属イオン捕捉
剤、珪酸塩、炭酸塩、硫酸塩などのアルカリ剤あ
るいは無機電解質、ポリビニルピロリドン、カル
ボキシメチルセルロースなどの再汚染防止剤、ア
ルカラーゼ、リパーゼ、セラローゼなどの酵素、
パラトルエンスルホン酸塩、スルホコハク酸塩、
タルク、カルシウムシリケートなどのケーキング
防止剤、過炭酸ナトリウム、過硼酸ナトリウム1
又は4水和物などの漂白剤、トリアセチルシアニ
ユレート、p−アセトキシベンゼンスルホン酸塩
ソーダなどの漂白活性化剤、ケイ酸マグネシウ
ム、硫酸マグネシウムなどの過酸化物の安定化
剤、第3ブチルヒドロキシトルエン、ギスチレン
化クレゾールなどの酸化防止剤、螢光染料、青味
付剤、香料などを含むことができるがこれについ
ては特に限定されず、目的に応じた配合がなされ
てよい。 〔発明の効果〕 本発明の洗浄剤組成物は、従来のゼオライト含
有洗剤では達成しえなかつた優た効果、即ち、綿
布、化学繊維の両者に対し良好な再汚染防止能を
示す。 〔実施例〕 以下に実施例を示し、本発明を更に説明する。 実施例 1 表1に示す配合の洗浄剤組成物(1〜5は本発
明品、6〜9は比較品)についての再汚染防止能
を以下の方法により評価した。結果を表1に併せ
て示す。 再汚染防止能評価試験法 試験布 綿ブロード、ナイロントリコツト 10
cm 10cm各々3枚 汚 れ カーボンブラツク0.25g/及びクレ
イ2.5g/ 条 件 温度 20℃ 硬度 4DH 濃度 0.133% トーゴトメータ 100r.p.m.10分汚染 浴比 試験布12枚/ 流水すすぎ 汚染液調整 洗液に汚れ成分(カーボンブラツク0.25gある
いはクルイ2.5g)を入れよく撹拌し更に超音波
分散機で完全に分散させ直ちにターゴトメーター
で汚染させる。 乾燥 プレス130℃、30sec 測定 4種類の各繊維の原布と汚染された試験
布の反射率を測定し 再汚染防止率(%)=R(S)*100/R(O) R(O)=原布の反射率 R(S)=汚染後の反射率 の式により再汚染防止率を求める。 【表】
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a detergent composition that is excellent in preventing re-staining during washing. [Prior Art] With the recent development of the petrochemical industry, the proportion of synthetic fibers in clothing has increased. Most chemical fibers are made of hydrophobic substances, so they have a very high affinity for oily substances. Therefore, dirt removed during washing is redeposited due to electrostatic attraction, etc., which is a major cause of darkening of clothes. By the way, as a restaining prevention agent for stains, CMC is used for cotton, and water-soluble polymers such as PEG and PVA are said to be effective for chemical fibers. Conventionally, polyphosphoric acid has been used as a detergent builder, but due to environmental concerns, it has been replaced with zeolite. [Problems to be Solved by the Invention] However, although this zeolite is excellent in water softening action, it is extremely poor in other builder properties such as dirt dispersion ability and buffering ability. The same goes for the re-fouling prevention ability, and even when PEG and CMC are used together, it is not as good as detergents using polyphosphates. [Means to solve the problem] Therefore, as a result of intensive research to provide a phosphorus-free detergent using zeolite that has good recontamination prevention ability, we found that α-sulfo fatty acid ester salt and Purlock type detergent It has been discovered that adding PEG to a copolymer combination system has an excellent effect regardless of whether the fabric to be washed is cotton fabric or chemical fiber, and based on this knowledge, the present invention has been completed. That is, the present invention comprises the following four components (a), (b), (c) and (d) (a) General formula (1) (However, R 1 is a C 6 - C 20 alkyl group, R 2 is a C 1 -
( b ) General formula (2) (However, m and p are numbers from 5 to 100, and n is a number from 5 to 200) 0.1 to 20% by weight of a Pluronic copolymer (c) 0.5 to 20% by weight of polyethylene glycol with an average molecular weight of 1000 to 20,000 (d) A cleaning composition containing 5 to 35% by weight of zeolite is provided. The α-sulfo fatty acid ester salt which is component (a) of the composition of the present invention has 10 to 20 carbon atoms, preferably
Mention may be made of derivatives of esters of linear saturated fatty acids having 12 to 18 carbon atoms and saturated monohydric alcohols having 1 to 3 carbon atoms, preferably methanol and ethanol. Sodium salts of sulfo fatty acid esters prepared from natural hydrogenated fatty acids and fatty acid polymers, such as stearic acid methyl ester, palmitic acid ethyl ester, hydrogenated palm kernel fatty acid methyl ester or hydrogenated tallow fatty acid methyl ester α-sulfonic acid Preference is given to using the sodium salt. α-Sulfofatty acid ester salts generally contain dependent amounts of α-sulfofatty acid disalts, which can result from hydrolysis of the ester bonds during industrial post-treatments, for example bleaching with H 2 O 2 or neutralization.
This di-salt is present in amounts of 5 to 25% by weight in industrial products without impairing the effectiveness of the product. In the following, α-sulfofatty acid ester salts therefore mean industrial di-salt-containing products. Component (a) is blended in an amount of 1 to 35% by weight, preferably in a range of 5 to 25% by weight. If it is less than 1% by weight, there is no sufficient effect, and even if it is added more than 35% by weight, no particular effect can be obtained. The Pluronic type copolymer of component (b) is represented by the above-mentioned general formula (2), where m and p are numbers from 5 to 100, and n is a number from 5 to 200, but preferably both m and np are 10.
~80. Also, the molecular weight is 900 or more, especially 1000~
10000 and the ethylene oxide content is 20-80% by weight,
Particularly preferred is 35 to 55% by weight. Component (b) is blended in a range of 0.1 to 20% by weight,
Preferably it is in the range of 1 to 10% by weight. If the amount is less than 0.1% by weight, no sufficient effect will be obtained, and if it is more than 20% by weight, no particular effect will be obtained. The polyethylene glycol component (c) has an average molecular weight of 1,000 to 20,000. average molecular weight
If it is less than 1,000 or more than 20,000, the re-contamination prevention ability will decrease when water hardness is high. It is recommended to mix this in the detergent in an amount of 0.5 to 20% by weight, preferably in a range of 1 to 10% by weight. At 0.5% by weight or less, there is no special effect, and at 20% by weight or more, the synergistic effect becomes constant. As the zeolite of component (d) in the composition of the present invention, commercially available zeolites such as A type, X type or amorphous synthetic zeolite can be used, and the content thereof is 5 to 35% by weight, preferably 10 ~
It is in the range of 20% by weight. If the content of this zeolite is less than 5% by weight, the physical properties of the powder during production will be poor, and moreover, satisfactory detergency will not be obtained.
If it exceeds % by weight, zeolite particles will adhere to the items to be washed, which is undesirable. The following various surfactants can be used in combination with the cleaning composition of the present invention. As anionic surfactants, linear or branched alkylbenzene sulfonates, alkyl or alkenyl ether sulfates, alkyl or alkenyl sulfates, olefin sulfonates, alkanesulfonates, saturated or unsaturated fatty acid salts, alkyl or Examples include alkenyl ether carboxylates, amino acid type surfactants, N-acylamino acid type surfactants, alkyl or alkenyl phosphates or salts thereof. The anionic surfactant is preferably blended in an amount of 15 to 35% by weight, including component (a), which is an essential component of the present invention, in a general detergent composition. Examples of amphoteric surfactants include carboxy or sulfobetaine type surfactants, and nonionic surfactants include polyoxyalkylene alkyl or alkenyl ethers, polyoxyethylene alkyl phenyl ethers, higher fatty acid alkanolamides or alkylene oxide additions thereof. Examples of cationic surfactants include quaternary ammonium salts, sucrose fatty acid esters, fatty acid esters, fatty acid glycerin monoesters, and alkylamine oxides. Other auxiliary additives commonly used in the composition of the present invention,
For example, phosphates such as tripolyphosphate, pyrophosphate,
Salts of ethane-1,1-diphosphonic acid, salts of phosphonocarboxylic acids such as 2-phosphonobutane-1,2-dicarboxylic acid, salts of amino acids such as aspartic acid and glutamic acid, nitrilotriacetate, ethylenediamitetraacetate, etc. Divalent metal ion scavengers such as polyelectrolytes such as aminopolyacetate, polyacrylic acid, and polyaconitic acid, non-dissociated polymers such as polyvinyl alcohol and polyvinylpyrrolidone, and salts of organic acids such as diglycolic acid and oricicarboxylate. , alkaline agents or inorganic electrolytes such as silicates, carbonates, and sulfates, recontamination inhibitors such as polyvinylpyrrolidone and carboxymethylcellulose, enzymes such as alcalase, lipase, and cellulose,
paratoluenesulfonate, sulfosuccinate,
Anti-caking agents such as talc and calcium silicate, sodium percarbonate, sodium perborate 1
or bleaching agents such as tetrahydrate, bleach activators such as triacetyl cyanurate, sodium p-acetoxybenzenesulfonate, peroxide stabilizers such as magnesium silicate, magnesium sulfate, tertiary butyl It may contain antioxidants such as hydroxytoluene and gistyrenated cresol, fluorescent dyes, blue tints, fragrances, etc., but these are not particularly limited and may be blended depending on the purpose. [Effects of the Invention] The detergent composition of the present invention exhibits excellent effects that could not be achieved with conventional zeolite-containing detergents, that is, good re-stain prevention ability for both cotton fabrics and synthetic fibers. [Example] The present invention will be further explained with reference to Examples below. Example 1 The recontamination prevention ability of cleaning compositions having the formulations shown in Table 1 (1 to 5 are inventive products and 6 to 9 are comparative products) was evaluated by the following method. The results are also shown in Table 1. Recontamination prevention ability evaluation test method Test cloth Cotton broadcloth, nylon tricot 10
cm 3 sheets each of 10cm Dirt Carbon black 0.25g/and clay 2.5g/ Conditions Temperature 20℃ Hardness 4DH Concentration 0.133% Togotometer 100r.pm 10 minutes contaminated Bath ratio 12 test cloths / Rinse with running water Adjust contaminated solution Dirt components in washing solution Add (0.25 g of carbon black or 2.5 g of Klui), stir well, completely disperse using an ultrasonic disperser, and immediately contaminate with a tergotometer. Drying Press 130℃, 30sec Measurement Measure the reflectance of the original fabric of each of the four types of fibers and the contaminated test fabric. Recontamination prevention rate (%) = R(S) * 100/R(O) R(O) = Reflectance of original fabric R(S) = Reflectance after contamination Find the recontamination prevention rate using the formula. 【table】

Claims (1)

【特許請求の範囲】 1 下記4成分(a)、(b)、(c)及び(d) (a) 一般式(1) (但し、R1はC10〜C20のアルキル基、R2はC1
〜C4のアルキル基、Mはアルカリ金属又はア
ルカリ土類金属を示す)で表わされるα−スル
ホ脂肪酸エステル塩1〜35重量% (b) 一般式(2) (但し、m、pは5〜100の数、nは5〜200の
数を示す)で表わされるプルロニツク型コポリ
マー0.1〜20重量% (c) 平均分子量が1000〜20000のポリエチレング
リコール0.5〜20重量% (d) ゼオライト5〜35重量% を含有する洗浄剤組成物。
[Claims] 1. The following four components (a), (b), (c) and (d) (a) General formula (1) (However, R 1 is a C 10 to C 20 alkyl group, R 2 is a C 1
~ C4 alkyl group, M represents an alkali metal or alkaline earth metal) α-sulfo fatty acid ester salt 1 to 35% by weight (b) General formula (2) (However, m and p are numbers from 5 to 100, and n is a number from 5 to 200) 0.1 to 20% by weight of a Pluronic copolymer (c) 0.5 to 20% by weight of polyethylene glycol with an average molecular weight of 1000 to 20000 % (d) A cleaning composition containing 5 to 35% by weight of zeolite.
JP14436685A 1985-07-01 1985-07-01 Detergent composition Granted JPS624797A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14436685A JPS624797A (en) 1985-07-01 1985-07-01 Detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14436685A JPS624797A (en) 1985-07-01 1985-07-01 Detergent composition

Publications (2)

Publication Number Publication Date
JPS624797A JPS624797A (en) 1987-01-10
JPH0560520B2 true JPH0560520B2 (en) 1993-09-02

Family

ID=15360438

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14436685A Granted JPS624797A (en) 1985-07-01 1985-07-01 Detergent composition

Country Status (1)

Country Link
JP (1) JPS624797A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0791555B2 (en) * 1989-12-22 1995-10-04 株式会社資生堂 Cleaning composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS582400A (en) * 1981-06-04 1983-01-07 ユニリ−バ−・ナ−ムロ−ゼ・ベンノ−トシヤ−プ Manufacture of solubility-improved powdery detergent
JPS59221392A (en) * 1983-05-31 1984-12-12 ライオン株式会社 Phosphorus-free detergent composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS582400A (en) * 1981-06-04 1983-01-07 ユニリ−バ−・ナ−ムロ−ゼ・ベンノ−トシヤ−プ Manufacture of solubility-improved powdery detergent
JPS59221392A (en) * 1983-05-31 1984-12-12 ライオン株式会社 Phosphorus-free detergent composition

Also Published As

Publication number Publication date
JPS624797A (en) 1987-01-10

Similar Documents

Publication Publication Date Title
US6255274B1 (en) Use of comb polymers as soil release polymers
US3925224A (en) Detergent additive composition
JPH0559394A (en) Detergent composition
JP2007522922A (en) Detergents, bleaches, and water precipitation softening systems for dishwashers and dishwashing detergents
JPH04292697A (en) Detergent composition
US5750483A (en) Non-phosphate machine dishwashing compositions containing polycarboxylate polymers and nonionic graft copolymers of vinyl acetate and polyalkylene oxide
JPH0639593B2 (en) Detergent composition containing alkylbenzene sulphonate and alcohol ethoxy sulphate surfactant system
JPH068434B2 (en) Cleaning composition for clothes
DE102007003885A1 (en) Use of a builder system comprising alkali metal tripolyphosphate and iminodisuccinic acid to produce automatic dishwasher formulations
CA1052220A (en) Detergent composition
GB2129457A (en) Stabilized bleaching and laundering composition
US3751370A (en) Low-foaming rinsing washing and cleaning compositions
US20160075972A1 (en) Formulations, their use as or for producing dishwashing detergents and their production
US3708427A (en) Washing and cleansing compositions
JP2008001770A (en) Detergent composition and cleaning method
GB2397823A (en) Aqueous cleaning compositions
JPS601918B2 (en) Phosphorus-free detergent composition with low recontamination
JPH0892591A (en) Nonionic powdery detergent composition
JPH0560520B2 (en)
JPS62240397A (en) Detergent composition
JP2831639B2 (en) Detergent composition
EP0711277B1 (en) Amido peroxycarboxylic acids for bleaching
US3703469A (en) Low-foaming rinsing,washing and cleaning compositions
CA1293668C (en) Detergent composition of improved oily soil removing capability
US20020123447A1 (en) Layered silicate built laundry detergent composition

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term