JPS5951598B2 - Method for preventing deposits, drying marks and thin film formation during final rinsing operation - Google Patents
Method for preventing deposits, drying marks and thin film formation during final rinsing operationInfo
- Publication number
- JPS5951598B2 JPS5951598B2 JP51047600A JP4760076A JPS5951598B2 JP S5951598 B2 JPS5951598 B2 JP S5951598B2 JP 51047600 A JP51047600 A JP 51047600A JP 4760076 A JP4760076 A JP 4760076A JP S5951598 B2 JPS5951598 B2 JP S5951598B2
- Authority
- JP
- Japan
- Prior art keywords
- hardness
- film formation
- deposits
- concentration
- weight
- 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
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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0047—Other compounding ingredients characterised by their effect pH regulated compositions
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/30—Sulfonation products derived from lignin
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)
- Detergent Compositions (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Description
【発明の詳細な説明】
本発明は硬水での最終滌ぎ作業においてガラス面、ラツ
カー塗布面又は金属面上に付着物、乾燥跡形及び薄膜形
成されるのを防ぐ方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for preventing deposits, dry marks and film formation on glass, lacquered or metal surfaces during final rinsing operations in hard water.
例えば自動車洗浄又は旅客列車洗浄の場合の様にガラス
、ラック塗布面又は金属面を酸性、中性1又はアルカリ
性洗浄した後で硬水で最終滌ぎを行うと、特にガラス面
、ラック塗布面又は金属面上に付着物、乾燥跡形又は薄
膜が形成されて、表面を見苦しくする。その様な乾燥跡
形、付着物及び薄膜の原因は一つは水中に含有される塩
であり、他は洗浄溶液の残滓である。一般に最終滌ぎ作
業のために完全に脱塩された水を十分な量で使用し得な
いから硬水が使用され、それにもかかわらず付着物や薄
膜形成のない明澄な表面仕上が望まれる。J 食器洗滌
機に使用されている様なクリヤリンスで実験を試みたが
成果はなかつた。If glass, rack-coated surfaces or metal surfaces are washed in acidic, neutral or alkaline conditions, followed by a final rinse with hard water, as is the case, for example, in automobile washing or passenger train cleaning, glass, rack-coated surfaces or metal surfaces may be damaged. Deposits, dry marks or films form on the surface, making the surface unsightly. The causes of such drying marks, deposits and films are, on the one hand, salts contained in the water, and on the other hand, residues of the cleaning solution. Hard water is generally used because fully desalinated water is not available in sufficient quantities for the final washing operation, yet a clear surface finish free of deposits and film formation is desired. J I tried experimenting with a clear rinse like the one used in dishwashers, but with no results.
硬水を使用すると見苦しい付着物や薄膜形成が生じた。
更にクリヤリンスは酸性に調整されていることが多く、
特に旅客列車の洗浄の場合にはこの酸のために鉄、塩な
いしは鉄錯塩が形成されて障害となる。ところで本発明
の方法を用いると硬水で滌ぐ場合にも付着物や条痕や薄
膜形成のないガラス面、ラック塗布面又金属面が得られ
ることが見出された。同方法は1価の陽イオン又はマグ
ネシウムをノ有する1種以上のリグニンスルホン酸の塩
を0.02〜0.04重量%/硬度の濃度で含有するp
H値4〜8の溶液で被洗滌面を温度4〜40℃において
処理することを特徴とする。1価の陽イオンを有するリ
グニンスルホン酸の丁塩としてはアルカリ金属塩例えば
特にナトリウム塩及びカリウム塩を使用することが出来
る。Use of hard water resulted in unsightly deposits and film formation.
Furthermore, clear rinses are often adjusted to be acidic.
Particularly in the case of cleaning passenger trains, this acid causes the formation of iron, salts, or iron complexes, which pose a problem. By the way, it has been found that by using the method of the present invention, a glass surface, a rack-coated surface, or a metal surface without deposits, streaks, or thin film formation can be obtained even when rinsed with hard water. The method involves the use of a polymer containing monovalent cations or one or more salts of lignin sulfonic acid containing magnesium at a concentration of 0.02 to 0.04% by weight/hardness.
It is characterized in that the surface to be cleaned is treated with a solution having an H value of 4 to 8 at a temperature of 4 to 40°C. As salts of ligninsulfonic acid with monovalent cations it is possible to use alkali metal salts, such as in particular the sodium and potassium salts.
l価の陽イオンとしては本発明の意義においてアンモニ
ウムも該当する。更にリグニンスルホン酸のマグネシウ
ム塩も本発明方法のために適する。リグニンスルホン酸
塩の濃度は使用滌ぎ水の硬度によつて定めるべき0.0
2〜0.04重量%/硬度の範囲であろう。本発明方法
のある有利な実施形式においては最終滌ぎ用の溶液に付
加的に界面活性剤を、使用リグニンスルホン酸塩に対し
て、l−15%の濃度で添加する。Ammonium also falls under the meaning of the present invention as a l-valent cation. Furthermore, magnesium salts of ligninsulfonic acid are also suitable for the process according to the invention. The concentration of lignin sulfonate should be determined by the hardness of the rinsing water used.
It will range from 2 to 0.04% by weight/hardness. In one advantageous embodiment of the process according to the invention, a surfactant is additionally added to the final washing solution in a concentration of 1-15%, based on the lignin sulfonate used.
この含界面活性剤最終滌ぎ溶液においてはリグニンスル
ホン酸塩の濃度は0.004〜0.04%/硬度である
ことが出来る。界面活性剤としては脂肪酸ジエタノール
アミド、アルキルベンゾールスルホン酸塩、脂肪族アル
コールポリグリコールエーテル及びアルキルフエノール
ポリグリコールエーテル又はそれらの混合物が適する。In this surfactant-containing final washing solution, the concentration of lignosulfonate can be from 0.004 to 0.04%/hardness. Suitable surfactants are fatty acid diethanolamides, alkylbenzole sulfonates, fatty alcohol polyglycol ethers and alkylphenol polyglycol ethers, or mixtures thereof.
ポリダリコールエーテルの場合には疎水性分子部分の炭
素原子当り0.25〜0.6のグリコール基を含有する
ものが適する。溶液のPH値は4〜8の範囲であるべき
である。In the case of polydarycol ethers, those containing 0.25 to 0.6 glycol groups per carbon atom of the hydrophobic molecule are suitable. The pH value of the solution should be in the range 4-8.
最終滌ぎ溶液中に塩及び界面活性剤を添加してこのPH
値の範囲が達せられない場合には、小量のアルカリ又は
酸の添加により所望に値に調整する。最終滌ぎは一般に
その都度の大気温度において行なわれるが、4 〜40
℃が有利な温度範囲であることが立証された。Add salts and surfactants to the final washing solution to adjust the pH.
If the value range cannot be reached, the desired value is adjusted by adding small amounts of alkali or acid. The final rinsing is generally carried out at the respective ambient temperature;
℃ has proven to be an advantageous temperature range.
上記の方法によつて硬水での最終滌ぎの場合でも、例え
ばガラス面、ラツク塗布面又は金属面上において付着物
、条痕及び薄膜形成のない面を得ることが出来る。The method described above makes it possible to obtain surfaces free of deposits, streaks and film formations, for example on glass surfaces, lightly coated surfaces or metal surfaces, even in the case of final washing with hard water.
すなわち例えばアルカリ性又は酸性液で洗浄された旅客
列車をその様に滌ぐ場合薄膜や条痕形成のない申分なく
明澄な窓が得られるし、又車体のラツク塗布面又は精鋼
表面も完全に斑痕のない外観を示す。同様に洗浄された
自動車を本発明による溶液で最終的に滌ぐと細縞や条.
痕形成のない明澄な窓ガラス並びに完全に斑痕のないラ
ツク塗布面、クロムー及びアルミニウム部分が得られる
ことが立証された。以下の実施例中の量記載は、別に記
載のない限り、重量%である。This means that, for example, when passenger trains that have been cleaned with alkaline or acidic liquids are washed in such a way, perfectly clear windows are obtained without the formation of films or streaks, and also the lightly coated or steel surfaces of the car body are thoroughly cleaned. Shows a spotless appearance. When a similarly cleaned car is finally rinsed with the solution according to the invention, no stripes or streaks appear.
It has been demonstrated that clear window panes without markings and completely mark-free easily coated surfaces, chrome and aluminum parts are obtained. Quantities stated in the following examples are in % by weight, unless otherwise stated.
例1
自動車を高圧装置を用い弱アルカリ性洗浄剤で洗浄し、
硬度16゜の水で滌いだ。Example 1: Washing a car with a weak alkaline detergent using a high-pressure device,
It was washed with water with a hardness of 16°.
引続いて同自動車を温度10℃において、硬度16゜の
水中にリグニンスルホン酸ナトリウム0.12%並びに
非イオン界面活性剤(デシルアルコールへの酸化エチレ
ン3モルの付加生成物)0.006%を含有するPH値
6.0の、同様に温度10℃に保持されている溶液で滌
丁ぎ、大気乾燥した。この様に滌ぎ、乾燥された自動車
には、その窓ガラス、クロムー及びアルミニウム部分に
も又ラツク塗布面にも付着物、条痕及び薄膜形成が見ら
れなかつた。Subsequently, the same car was heated to a temperature of 10°C, and 0.12% of sodium lignin sulfonate and 0.006% of a nonionic surfactant (addition product of 3 moles of ethylene oxide to decyl alcohol) were added to water with a hardness of 16°. It was washed with a solution containing a pH value of 6.0 and kept at a temperature of 10° C., and then dried in the air. The automobiles washed and dried in this manner showed no deposits, streaks or film formation on the window glass, chrome and aluminum parts, or on the lightly coated surfaces.
ク 硬度16゜の水中にはリダニンスルホン酸塩0.0
3%とデシルアルコール酸化エチレン3モルの付加生成
物0.0015%とのみを含有する溶液と最終滌ぎに使
用すると、自動車の乾燥後に条痕及び薄膜形成がはつき
りと見られた。h) In water with a hardness of 16°, there is 0.0 of ridanine sulfonate.
When a solution containing only 3% and 0.0015% of the addition product of 3 moles of ethylene oxide decyl alcohol was used for the final cleaning, the streaks and film formation were clearly visible after drying the car.
i例 2
窓ガラスを酸性洗浄剤で塵及び沈殿物を除去してから硬
度16゜の水で滌いだ。Example 2 A window glass was cleaned with acidic cleaning agent to remove dust and sediment, and then rinsed with water having a hardness of 16°.
次いで硬度16゜の水中にスルホン化度(スルホン酸基
/フエニルプロパン単位の数値)約0.17のリグニン
スルホン酸フナトリウム0.5%を含有する溶液で温度
15℃において最終滌ぎを行なつた。同溶液のPH値は
7.5であつた。大気乾燥後に窓ガラスは完全に明澄で
あり、条痕、薄膜又は斑点はなかつた。硬度4゜の水に
リグニンスルホン酸ナトリウム.(硫黄含量6.5%、
Na。A final washing was then carried out at a temperature of 15° C. in a solution containing 0.5% of sodium lignosulfonate with a degree of sulfonation (number of sulfonic acid groups/phenylpropane units) of approximately 0.17 in water with a hardness of 16°. Summer. The pH value of the solution was 7.5. After air drying, the window glass was completely clear, with no streaks, films or spots. Sodium lignin sulfonate in water with a hardness of 4°. (Sulfur content 6.5%,
Na.
O含量10%、グリコース含量10%以下、糖含量4%
以下)0.02%及びデシルアルコール酸化エチレン3
モルの付加生成物0.001%を含有する溶液で最終滌
ぎを行つた場合にも同じ結果が得られた。例2の2番目
の実験における様な低いリグニンスルホン酸塩−及び湿
潤剤濃度を硬度16゜の水に適用すると乾燥後に窓ガラ
スの下半分に見苦しい著しい薄膜形成が見られた。O content 10%, glycose content 10% or less, sugar content 4%
Below) 0.02% and decyl alcohol ethylene oxide 3
The same results were obtained when the final washing was carried out with a solution containing 0.001% molar addition product. When low lignin sulfonate and wetting agent concentrations, such as in the second run of Example 2, were applied to 16° hardness water, significant unsightly film formation was observed on the lower half of the window glass after drying.
例3
窓ガラスを酸性洗浄剤で塵及び沈殿物を除去し、硬度1
6゜の水で滌いだ。Example 3 Dust and sediments are removed from window glass with acidic cleaning agent, and the hardness is 1
Rinse with 6° water.
引続いてリグニンスルホン酸ナトリウム0.1%を添加
されている硬度16゜の水で温度19℃において最終滌
ぎを行なつた。同溶液のPH値は7.0であつた。乾燥
後に窓ガラスの下半分になお薄膜形成が見られた。それ
に対して上記の最終滌ぎ溶液になお非イオン界面活性剤
(デシルアルコールへの酸化エチレン3モルの付加生成
物)0.005%を添加すると窓ガラスは明澄になり、
薄膜、条痕及び斑点がなくなつた。デシルアルコールへ
の酸化エチレン3モルの付加生成物0.005%のみを
添加されている硬度16゜の水で最終滌ぎを行うと、乾
燥後窓ガラスに均一に分配された薄膜が見られた。例4
窓ガラスを例2に記述されている様にして洗浄し、滌い
だ。A final washing was then carried out at a temperature of 19 DEG C. with water having a hardness of 16 DEG to which 0.1% sodium ligninsulfonate had been added. The pH value of the solution was 7.0. After drying, a thin film formation was still observed on the lower half of the window glass. On the other hand, if 0.005% of a nonionic surfactant (addition product of 3 moles of ethylene oxide to decyl alcohol) was added to the final washing solution, the window glass became clear.
Films, streaks and spots disappeared. A final rinse with 16° hardness water to which only 0.005% of the addition product of 3 moles of ethylene oxide to decyl alcohol was added resulted in an evenly distributed thin film on the window glass after drying. . Example 4 Window glass was cleaned and scrubbed as described in Example 2.
最終滌ぎはリグニンスルホン酸ナトリウム0.25%と
やし油脂肪酸ジエタノールアミド0.02%を含有する
硬度22゜の水で行つた。同溶液のPH値は4.5に調
整された。乾燥後に薄膜及び条痕のない明澄なガラス面
が得られた。硬度16゜の水にリグニンスルホン酸マグ
ネシウム(MgO約7.5%)0.2%及びデシルアル
コールへの酸化エチレン3モルの付加生成物0.01%
を添加した溶液で最終滌ぎを行つた場合にも、同様に条
痕及び薄膜の完全にない明澄な窓ガラスが得られた。The final washing was carried out with 22° hardness water containing 0.25% sodium ligninsulfonate and 0.02% coconut oil fatty acid diethanolamide. The pH value of the solution was adjusted to 4.5. After drying, a clear glass surface without films and streaks was obtained. 0.2% of magnesium lignosulfonate (approximately 7.5% MgO) and 0.01% of addition product of 3 moles of ethylene oxide to decyl alcohol in 16° hardness water.
Similarly, clear window glass completely free of streaks and thin films was obtained when final washing was carried out with a solution containing .
リグニンスルホン酸マグネシウムの代りにリグニンスル
ホン酸カルシウムを0.2〜0.4%の濃度で使用した
場合には窓ガラスになお明らかな薄膜が見られた。When calcium lignosulfonate was used instead of magnesium lignosulfonate at a concentration of 0.2-0.4%, a still obvious thin film was seen on the window glass.
硬度16゜の水にリグニンスルホン酸カリウム0.2〜
0.4%とノニルフエノールへの酸化エチレン5モルの
付加生成物0.01%ないしはドデシルベンゾールスル
ホン酸ナトリウムとノニフエノールへの酸化エチレン4
モルの付加生成物との混合物0.02%を添加した溶液
で最終滌ぎを行つた場合にも薄膜、斑点及び条痕の完全
にない明澄な窓ガラスが得られた。Potassium lignin sulfonate 0.2~ in water with hardness of 16°
Addition product of 5 moles of ethylene oxide to nonylphenol with 0.4% or 4 moles of ethylene oxide to sodium dodecylbenzole sulfonate and nonylphenol
Even when the final cleaning was carried out with a solution to which 0.02% of the mixture with the molar addition product was added, a clear window glass completely free of films, spots and streaks was obtained.
Claims (1)
布面又は金属面上に付着物、乾燥跡形及び薄膜が形成さ
れるのを防ぐ方法において、同表面1価の陽イオン又は
マグネシウムを含有する1種以上のリグニンスルホン酸
の塩をa)0.02〜0.04重量%/硬度 の濃度で含有するか。 又は有利には同塩をb)0.004〜0.04重量%/
硬度 の濃度で及び付加的に界面活性剤をリグニンスルホン酸
塩に対して1〜15重量%の濃度で含有する、pH値4
〜8の溶液で4〜40℃の温度において処理することを
特徴とする最終滌ぎ作業において付着物、乾燥跡形及び
薄膜形成を防止するための方法。 2 溶液が界面活性剤として脂肪酸ジエタノールアミド
及び/又は疎水性分子部分の炭素原子当りグリコール基
0.25〜0.6を有する脂肪族アルコール−又はアル
キルフェノールポリグリコールエーテル及び/又はアル
キルベンゾールスルホン酸塩を含有する特許請求の範囲
第1項記載の方法。[Scope of Claims] 1. A method for preventing the formation of deposits, drying marks, and thin films on glass surfaces, rack-coated surfaces, or metal surfaces during final washing with hard water, comprising monovalent cations on the same surfaces. or one or more salts of lignin sulfonic acid containing magnesium at a) concentration of 0.02 to 0.04% by weight/hardness. or advantageously the same salt b) 0.004 to 0.04% by weight/
pH value 4, containing a hardness concentration and additionally a surfactant in a concentration of 1 to 15% by weight, based on the lignin sulfonate.
A method for preventing deposits, drying marks and film formation in the final rinsing operation, characterized by treatment with a solution of 1 to 8 at a temperature of 4 to 40°C. 2 The solution contains fatty acid diethanolamide and/or aliphatic alcohol having 0.25 to 0.6 glycol groups per carbon atom of the hydrophobic molecule moiety as a surfactant, or an alkylphenol polyglycol ether and/or an alkylbenzole sulfonate. A method according to claim 1 containing:
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2518391A DE2518391C2 (en) | 1975-04-25 | 1975-04-25 | Process to prevent deposits, drying out and haze during rinsing processes |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS51130689A JPS51130689A (en) | 1976-11-13 |
JPS5951598B2 true JPS5951598B2 (en) | 1984-12-14 |
Family
ID=5944972
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51047600A Expired JPS5951598B2 (en) | 1975-04-25 | 1976-04-26 | Method for preventing deposits, drying marks and thin film formation during final rinsing operation |
Country Status (12)
Country | Link |
---|---|
JP (1) | JPS5951598B2 (en) |
AT (1) | AT346447B (en) |
BE (1) | BE841047A (en) |
CH (1) | CH619261A5 (en) |
DE (1) | DE2518391C2 (en) |
ES (1) | ES447271A1 (en) |
FR (1) | FR2308431A1 (en) |
GB (1) | GB1485606A (en) |
IT (1) | IT1063216B (en) |
NL (1) | NL182490C (en) |
SE (1) | SE414786B (en) |
ZA (1) | ZA762454B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5104584A (en) * | 1990-06-22 | 1992-04-14 | The Clorox Company | Composition and method for fabric encrustation prevention comprising a lignin derivative |
CA2047928A1 (en) * | 1990-07-27 | 1992-01-28 | Munehiro Nogi | Method and apparatus for washing dishes, sticking inhibitor and rinsing assistant |
DE19859777A1 (en) * | 1998-12-23 | 2000-06-29 | Henkel Kgaa | Detergent for hard surfaces |
DE19859808A1 (en) * | 1998-12-23 | 2000-06-29 | Henkel Kgaa | Multi-phase cleaning agent with lignin sulfonate |
-
1975
- 1975-04-25 DE DE2518391A patent/DE2518391C2/en not_active Expired
-
1976
- 1976-03-05 SE SE7603054A patent/SE414786B/en not_active IP Right Cessation
- 1976-03-05 NL NLAANVRAGE7602357,A patent/NL182490C/en not_active IP Right Cessation
- 1976-04-22 FR FR7611813A patent/FR2308431A1/en active Granted
- 1976-04-22 IT IT22538/76A patent/IT1063216B/en active
- 1976-04-23 ZA ZA762454A patent/ZA762454B/en unknown
- 1976-04-23 ES ES447271A patent/ES447271A1/en not_active Expired
- 1976-04-23 GB GB16459/76A patent/GB1485606A/en not_active Expired
- 1976-04-23 AT AT298376A patent/AT346447B/en not_active IP Right Cessation
- 1976-04-23 CH CH516476A patent/CH619261A5/en not_active IP Right Cessation
- 1976-04-23 BE BE166393A patent/BE841047A/en not_active IP Right Cessation
- 1976-04-26 JP JP51047600A patent/JPS5951598B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
SE414786B (en) | 1980-08-18 |
FR2308431B1 (en) | 1980-03-28 |
AT346447B (en) | 1978-11-10 |
SE7603054L (en) | 1976-10-26 |
NL182490C (en) | 1988-03-16 |
IT1063216B (en) | 1985-02-11 |
ATA298376A (en) | 1978-03-15 |
GB1485606A (en) | 1977-09-14 |
BE841047A (en) | 1976-10-25 |
CH619261A5 (en) | 1980-09-15 |
NL182490B (en) | 1987-10-16 |
NL7602357A (en) | 1976-10-27 |
JPS51130689A (en) | 1976-11-13 |
DE2518391C2 (en) | 1983-10-06 |
ES447271A1 (en) | 1977-12-16 |
DE2518391A1 (en) | 1976-11-04 |
ZA762454B (en) | 1977-04-27 |
FR2308431A1 (en) | 1976-11-19 |
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