JPS5845996B2 - cleaning composition - Google Patents

cleaning composition

Info

Publication number
JPS5845996B2
JPS5845996B2 JP10244476A JP10244476A JPS5845996B2 JP S5845996 B2 JPS5845996 B2 JP S5845996B2 JP 10244476 A JP10244476 A JP 10244476A JP 10244476 A JP10244476 A JP 10244476A JP S5845996 B2 JPS5845996 B2 JP S5845996B2
Authority
JP
Japan
Prior art keywords
cleaning composition
sodium
peg
alkaline earth
washed
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
JP10244476A
Other languages
Japanese (ja)
Other versions
JPS5327603A (en
Inventor
統 奥村
武信 阪谷
信夫 宮本
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 JP10244476A priority Critical patent/JPS5845996B2/en
Publication of JPS5327603A publication Critical patent/JPS5327603A/en
Publication of JPS5845996B2 publication Critical patent/JPS5845996B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明はα−スルホ脂肪酸エステル塩(α−8FE)及
びオレフィンスルホン酸塩(O8)を活性性分とする、
起泡力等の性能に優れた洗浄剤組成物に関する。
Detailed Description of the Invention The present invention uses α-sulfo fatty acid ester salt (α-8FE) and olefin sulfonate (O8) as active ingredients,
The present invention relates to a cleaning composition having excellent foaming power and other properties.

直鎖アルキルベンゼンスルホネー)(LAS)は現在で
も洗浄剤の主要な活性成分の一つとして多用されている
が、近年の水質汚染等の問題から、硬水中でも洗浄力を
有し、かつ、生分解性の特に良好な活性剤が使用される
方向にある。
Linear alkylbenzene sulfone (LAS) is still widely used as one of the main active ingredients in cleaning agents, but due to recent problems such as water pollution, it has been found that it has detergency even in hard water and is biodegradable. There is a trend toward using active agents with particularly good properties.

このような活性剤にはアルキルサルフエー)(AS)、
アルキルエーテルサルフェート(AES)、O8あるい
はα−8FEなどが挙げられるが、αSFEは特に好適
な活性剤である。
Such activators include alkyl sulfates (AS),
Examples include alkyl ether sulfate (AES), O8 or α-8FE, with αSFE being a particularly preferred activator.

しかし、αSFEを活性成分とする有燐又は無燐洗剤は
O8やLASを活性成分とするものに比べて洗浄力は充
分満足できるが、特に起泡力が劣り、又αSFE又はO
8を活性成分とする洗浄剤は特に高硬度水に使用すると
、活性剤のアルカリ土類金属塩が被洗布(特に肌着、シ
ーツ等の綿布やオシャレ着のようなポリエステル布)に
沈着して被洗布の黄変化を起こし、又被洗布が難燃加工
されているもの(例えばカーテン布)の場合はその難燃
効果を未加工布と同程度まで劣化させる等の欠点がある
However, although phosphorus-containing or phosphorus-free detergents containing αSFE as an active ingredient have satisfactory cleaning power compared to those containing O8 or LAS as an active ingredient, they are particularly inferior in foaming power, and
When detergents containing 8 as an active ingredient are used especially in highly hard water, the alkaline earth metal salts of the active agent may be deposited on the fabric being washed (especially cotton fabrics such as underwear and sheets, and polyester fabrics such as fashionable clothing). There are drawbacks such as yellowing of the cloth to be washed, and if the cloth to be washed is flame-retardant (for example, curtain cloth), its flame-retardant effect is degraded to the same level as untreated cloth.

又LASを活性成分とした洗浄剤では生分解性がやや劣
る上に被洗布に対する風合いが悪い等の欠点を有してい
る。
In addition, detergents containing LAS as an active ingredient have drawbacks such as slightly inferior biodegradability and poor texture on the cloth being washed.

本発明者らはα−8FEにO8及びポリエチレングリコ
ール(PEG)を加えることにより、それらの相剰効来
が発揮され、洗浄力は勿論、起泡力(泡高)及び生分解
性にすぐれ、被洗布に対しても黄変化を防止し、難燃効
果を阻害せず、しかも良好な風合いを与える洗浄剤組成
物が得られることを見出した。
The present inventors have demonstrated that by adding O8 and polyethylene glycol (PEG) to α-8FE, their mutual effects are exhibited, and the product has excellent detergency, foaming power (foam height), and biodegradability. It has been found that it is possible to obtain a cleaning composition that prevents yellowing of the cloth being washed, does not impede the flame retardant effect, and provides a good texture.

本発明はこのような知見に基づいて達成されたもので、 (但しR1:C6〜C2oのアルキル基、R2:C1〜
C3のアルキル基、 M:アルカリ金属及び/又はアルカリ土類金属) で示されるα−スルホ脂肪酸エステル塩、(1))
C10−C20のオレフィンスルホン酸のアルカリ金属
塩及び/又はアルカリ土類金属塩、及び(c) 平均
分子量1000〜10000のポリエチレングリコール を(a):(b)−9o : 10〜50 : 50
(重量比)及び(a) +(b) : (c)−100
〜1〜20 (重量比)で含有することを特徴とする洗
浄剤組成物を提供するにある。
The present invention was achieved based on such knowledge, (However, R1: C6-C2o alkyl group, R2: C1-C2o alkyl group,
C3 alkyl group, M: alkali metal and/or alkaline earth metal) α-sulfo fatty acid ester salt (1))
C10-C20 alkali metal salt and/or alkaline earth metal salt of olefin sulfonic acid, and (c) polyethylene glycol with average molecular weight 1000-10000 (a):(b)-9o: 10-50: 50
(weight ratio) and (a) + (b): (c) -100
It is an object of the present invention to provide a cleaning composition characterized in that it contains 1 to 20 (weight ratio).

本発明洗浄剤の活性成分として使用されるα−8FEは
前記一般式で示されるもので、脂肪酸エステルを通常の
連続薄膜型スルホン化装置又は種型スルホン化装置でス
ルホン化後、中和するか、或いは脂肪酸を前記装置でス
ルホン化し、更にC1〜C3のアルコールでエステル化
後、中和スることによって得られる。
α-8FE used as the active ingredient of the cleaning agent of the present invention is represented by the above general formula, and is obtained by sulfonating the fatty acid ester with a conventional continuous thin film sulfonation device or seed type sulfonation device and then neutralizing it. Alternatively, it can be obtained by sulfonating a fatty acid in the above-mentioned apparatus, further esterifying it with a C1-C3 alcohol, and then neutralizing it.

この場合の原料脂肪酸又は脂肪酸エステルとしては天然
油脂、例えばヤシ油、パーム核油、パーム油又は牛脂に
より誘導されたC8〜C22の脂肪酸又はそのエステル
(炭素鎖長C1〜C3)や、アルコール、オレフィン等
から誘導されたC3〜C22の合成脂肪酸又はそのエス
テル(炭素鎖長C1〜C3)が、又塩としてはアルカリ
金属塩、アルカリ土類金属塩又はそれらの混合物が使用
される。
In this case, the raw fatty acids or fatty acid esters include C8 to C22 fatty acids or their esters (carbon chain length C1 to C3) derived from natural fats and oils, such as coconut oil, palm kernel oil, palm oil, or beef tallow, alcohols, and olefins. Synthetic C3-C22 fatty acids or esters thereof (carbon chain length C1-C3) derived from etc. are used, and as salts, alkali metal salts, alkaline earth metal salts or mixtures thereof are used.

なおこのα−8FE中には一般式 (但しR1:C6〜C2oのアルキル基、M:アルカリ
金属及び/又はアルカリ土類金属)で示される化合物が
20%以下、好ましくは10%以下含まれていても良い
Note that this α-8FE contains 20% or less, preferably 10% or less of a compound represented by the general formula (R1: C6 to C2o alkyl group, M: alkali metal and/or alkaline earth metal). It's okay.

同様に活性成分として使用されるO8はオレフィンを通
常の連続薄膜型スルホン化装置でスルホン化後、中和、
加水分解して得られる。
Similarly, O8, which is used as an active ingredient, is used to sulfonate olefins in a conventional continuous thin-film sulfonation device, then neutralize them.
Obtained by hydrolysis.

この場合、原料オレフィンとしてはワックスクラッキン
グ法、チーグラー法による重合法、又はそれらの改良法
で得られるcio−c2oのα−オレフィン:C0°〜
C20のインナーオレフィン:Cxo=C2oのビニリ
デンオレフィン;及びそれらの混合物が使用される。
In this case, the raw material olefin is a cio-c2o α-olefin obtained by a wax cracking method, a Ziegler polymerization method, or an improved method thereof: C0°~
C20 inner olefins: Cxo=C2o vinylidene olefins; and mixtures thereof are used.

又塩としてはアルカリ金属塩、アルカリ土類金属塩及び
それらの混合物が使用される。
As the salt, alkali metal salts, alkaline earth metal salts and mixtures thereof are used.

以上の活性成分の他に本発明においては黄変化防止及び
難燃性保持の目的でPEGが使用される。
In addition to the above active ingredients, PEG is used in the present invention for the purpose of preventing yellowing and maintaining flame retardancy.

このPEGは分子量1000〜10000のものである
This PEG has a molecular weight of 1,000 to 10,000.

ここでα−8FEとO8との配合比率は重量比で90:
10〜50 : 50の範囲であり、又(α−8FE+
O8)とPEGとの配合比率は重量比で100: 1〜
20の範囲でなげればならない。
Here, the blending ratio of α-8FE and O8 is 90:
10 to 50: 50, and (α-8FE+
The blending ratio of O8) and PEG is 100:1 to 100:1 by weight.
You must throw within the range of 20.

これらの範囲内でのみ各成分による相剰効果が発揮され
、特に、すぐれた泡高、黄変防止、及び難燃性の保持を
達成することができる。
Only within these ranges can the additive effects of each component be exhibited, and in particular excellent foam height, prevention of yellowing, and maintenance of flame retardancy can be achieved.

換言すれば、前記範囲外ではこれらの効果は得られない
In other words, these effects cannot be obtained outside the above range.

本発明の組成物には更に公知の洗剤用添加剤として、例
えば珪酸ソーダ、炭酸ソーダ、トリポリリン酸ソーダ、
ピロリン酸ソーダ、オルソリン酸ソーダ、アルミノシリ
ケート等の無機ビルダー;無水マレイン酸〜オレフィン
共重合体のようなポリカルボン酸塩、クエン酸ソーダ、
オキシジコハク酸ソーダ、ニトリロトリ酢酸ソーダ(N
TA)等の有機ビルダー;EDTAのような有機キレー
ト剤;アンチケーキング剤;螢光増白剤;香料等が使用
できる。
The composition of the present invention may further include known detergent additives such as sodium silicate, sodium carbonate, sodium tripolyphosphate,
Inorganic builders such as sodium pyrophosphate, sodium orthophosphate, and aluminosilicate; polycarboxylate salts such as maleic anhydride and olefin copolymers, sodium citrate,
Sodium oxydisuccinate, Sodium nitrilotriacetate (N
Organic builders such as TA); organic chelating agents such as EDTA; anti-caking agents; fluorescent brighteners; fragrances, etc. can be used.

以下に実施例を示す。Examples are shown below.

実施例 1 下記処方に従って、硬化牛脂脂肪酸メチル及びC16〜
C18のα−オレフィンより夫々誘導されたナトリウム
α−スルホ脂肪酸メチル(α−8FMe−Na)、α−
オレフィンスルホン酸ナトリウム(AO8)及びPEG
(分子量6000)を主成分とする洗浄剤組成物を調製
した。
Example 1 According to the following formulation, hydrogenated beef tallow fatty acid methyl and C16~
Sodium α-sulfofatty acid methyl (α-8FMe-Na), α-
Sodium olefin sulfonate (AO8) and PEG
(molecular weight 6000) was prepared as a main component.

次にこの組成物の泡高を測定した結果は表−1の通りで
ある。
Next, the foam height of this composition was measured and the results are shown in Table 1.

処方 α−8FMe 25% 08 PEG □ 2%珪酸ソー
ダ 15%炭酸ナトリウム
10%硫酸ナトリウム及び水
バランス表−1の結果から判るように、α−8FM
e:AO8の配合比が90:10〜50:50の時、α
−8FMe及びAO8単品よりすぐれた泡高を示した。
Prescription α-8FMe 25% 08 PEG □ 2% Sodium silicate 15% Sodium carbonate
10% sodium sulfate and water
As can be seen from the results of balance table-1, α-8FM
e: When the blending ratio of AO8 is 90:10 to 50:50, α
-8FMe and AO8 exhibited superior foam height.

実施例 2 実施例1と同じ活性剤を用い、PEG(分子量6000
)の配合量を下記処方のように変化させた場合の泡高を
表−2に示した。
Example 2 Using the same active agent as in Example 1, PEG (molecular weight 6000
Table 2 shows the foam height when the blending amount of () was changed as shown in the following formulation.

処方 * 表−2の結果から判るように、PEGの配合量が活性剤
に対して1〜20%の場合に優れた大泡高を示した。
Formulation *As can be seen from the results in Table 2, excellent large foam height was exhibited when the amount of PEG was 1 to 20% based on the active agent.

実施例 3〜5 α−8FMe、O8及びPEGの種類を変えた他は実施
例1の/16.4と同じ組成の洗浄剤組成物を調製し、
泡高を測定した結果、表−3に示すように優れた泡高を
示した。
Examples 3 to 5 A cleaning composition having the same composition as /16.4 of Example 1 was prepared, except that the types of α-8FMe, O8 and PEG were changed,
As a result of measuring the foam height, as shown in Table 3, the foam height was excellent.

実施例 6 実施例2の/%10の洗浄剤組成物を用いて被洗**布
を洗浄し、黄変度及び難燃性を試験した結果を表−4に
示した。
Example 6 A cloth to be washed was washed using the cleaning composition of Example 2 with a ratio of /% 10, and the yellowing degree and flame retardance were tested. The results are shown in Table 4.

表−4の結果から判るように、PEGの配合量が活性剤
に対し1〜20%の範囲である時、被洗布の黄変化が防
止でき、且つ難燃性も保持できる。
As can be seen from the results in Table 4, when the blending amount of PEG is in the range of 1 to 20% based on the active agent, yellowing of the washed fabric can be prevented and flame retardancy can also be maintained.

実施例 7 下記処方にした他は実施例1と同じ活性剤及びPEGを
用いて洗浄剤組成物を調製し、泡高、被洗布の黄変度及
び難燃性を測定した結果、優れた泡高を示すと共に被洗
布の黄変化を防止し、又難燃性を保持することができた
Example 7 A cleaning composition was prepared using the same active agent and PEG as in Example 1 except for the following formulation, and the foam height, yellowing degree of the cloth to be washed, and flame retardancy were measured. As a result, it was found to be excellent. It was able to exhibit a high foam level, prevent yellowing of the washed fabric, and maintain flame retardancy.

処方 α−8FMe 15 % O8 PEG トリポリリン酸ソーダ 珪酸ナトリウム 炭酸ナトリウム 硫酸ナトリウム及び水 試験結果 泡高(m11L) 黄変性 10 % 2 % 15 % 10 % 5 % バランス 7 難燃性 炭化長(C1rL) 残炎時間(秒) 残しん時間(秒) 1.5 なお試験法は下記の通りである。prescription α-8FMe 15% O8 PEG Sodium tripolyphosphate Sodium silicate sodium carbonate sodium sulfate and water Test results Foam height (m11L) yellowing 10% 2% 15% 10% 5% balance 7 Flame retardance Carbonization length (C1rL) Afterflame time (seconds) Remaining time (seconds) 1.5 The test method is as follows.

泡高試験 有機汚垢物質を付けたシャツを、電気洗濯機中、湯量3
0J、浴比1:30、温度25°C1時間10分、3°
DHの水使用の条件で洗浄し、生じた泡の高さを測定す
る。
Foam height test: The shirt with the organic soiling substance was placed in an electric washing machine with a hot water volume of 3.
0J, bath ratio 1:30, temperature 25°C 1 hour 10 minutes, 3°
Wash under the conditions of using DH water and measure the height of the foam produced.

黄変化試験 洗浄−すすぎ−風乾のサイクルを20回繰返した後、カ
ールツアイス社製Elrephoで被洗布の反射率Ry
(緑色用フィルター使用)及びRz (青色用フィル
ター使用)を測定し、下記式よりb値を求める。
Yellowing test After repeating the washing-rinsing-air-drying cycle 20 times, the reflectance Ry of the washed fabric was measured using Elrepho manufactured by Carl Zeiss.
(using a filter for green color) and Rz (using a filter for blue color) are measured, and the b value is determined from the following formula.

一方、水洗浄のみの被洗布の反射率Ry及びRzを測定
しb値を求め、黄変度はその差(△b値)として表わす
On the other hand, the reflectances Ry and Rz of the cloth washed with water are measured to determine the b value, and the degree of yellowing is expressed as the difference (Δb value).

なお洗浄条件は湯量900m1.浴比1:30.温度2
5℃、時間10分、15°DHの水使用である。
The cleaning conditions are a hot water volume of 900ml. Bath ratio 1:30. temperature 2
Water was used at 5°C, for 10 minutes, and at 15°DH.

難燃性試験 難燃加工された布(ポリエステル布62%、レーヨン3
8%)を洗浄−すすぎ−風乾のサイクルで5回繰返し処
理して後、スガ試験機製垂直燃焼性試験器を用いてJI
S L−1091に従って試験した。
Flame retardant test Flame retardant fabric (62% polyester cloth, rayon 3
8%) in a washing-rinsing-air-drying cycle five times, and then tested using a vertical flammability tester made by Suga Test Instruments.
Tested according to SL-1091.

Claims (1)

【特許請求の範囲】 1(a)一般式 (但しR1:C6〜C2oのアルキル基、R2:C1〜
C3のアルキル基、 M:アルカリ金属及び/又はアルカリ土類金属)で示さ
れるα−スルホ脂肪酸エステル塩、(b) C10−
C20のオレフィンスルホン酸のアルカリ金属塩及び/
又はアルカリ土類金属塩、及び(c) 平均分子量1
000〜10000のポリエチレングリコール を(a):(b)−90: 10〜50 : 50 (
重量比)及び(a)+(b) :(c)= 100 :
1〜20 (重量比)で含有することを特徴とする洗
浄剤組成物。
[Claims] 1(a) General formula (wherein R1: C6 to C2o alkyl group, R2: C1 to
C3 alkyl group, M: α-sulfo fatty acid ester salt represented by alkali metal and/or alkaline earth metal), (b) C10-
C20 olefin sulfonic acid alkali metal salt and/or
or an alkaline earth metal salt, and (c) an average molecular weight of 1
000-10000 polyethylene glycol (a):(b)-90:10-50:50 (
weight ratio) and (a) + (b): (c) = 100:
A cleaning composition characterized by containing 1 to 20 (weight ratio).
JP10244476A 1976-08-27 1976-08-27 cleaning composition Expired JPS5845996B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10244476A JPS5845996B2 (en) 1976-08-27 1976-08-27 cleaning composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10244476A JPS5845996B2 (en) 1976-08-27 1976-08-27 cleaning composition

Publications (2)

Publication Number Publication Date
JPS5327603A JPS5327603A (en) 1978-03-15
JPS5845996B2 true JPS5845996B2 (en) 1983-10-13

Family

ID=14327627

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10244476A Expired JPS5845996B2 (en) 1976-08-27 1976-08-27 cleaning composition

Country Status (1)

Country Link
JP (1) JPS5845996B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5123708A (en) * 1975-06-24 1976-02-25 Tokyo Shibaura Electric Co KASETSUTOSHIKITEEPURE KOODA
CA1206060A (en) * 1981-12-24 1986-06-17 Peter K. Church Oil and grease emulsification system
JPS59221393A (en) * 1983-05-31 1984-12-12 ライオン株式会社 Detergent composition
US5429773A (en) * 1993-02-05 1995-07-04 The Procter & Gamble Company Process to improve alkyl ester sulfonate surfactant compositions
KR100209789B1 (en) * 1993-10-12 1999-07-15 제프리 더블유. 버틀렛 Liquid detergent compositions comprising salt of alpha sulfonated fatty acid methyl esters and anionic surfactants
US5965508A (en) * 1997-10-21 1999-10-12 Stepan Company Soap bar compositions comprising alpha sulfonated fatty acid alkyl esters and long chain fatty acids

Also Published As

Publication number Publication date
JPS5327603A (en) 1978-03-15

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