EP0040713B1 - Verwendung von Alkylpolyglykolethermischformale zur Schaumverhütung - Google Patents
Verwendung von Alkylpolyglykolethermischformale zur Schaumverhütung Download PDFInfo
- Publication number
- EP0040713B1 EP0040713B1 EP81103326A EP81103326A EP0040713B1 EP 0040713 B1 EP0040713 B1 EP 0040713B1 EP 81103326 A EP81103326 A EP 81103326A EP 81103326 A EP81103326 A EP 81103326A EP 0040713 B1 EP0040713 B1 EP 0040713B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mixed formals
- agents
- alkali
- cleaning
- cleaning agents
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
- C11D1/721—End blocked ethers
-
- 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
- C11D3/0026—Low foaming or foam regulating compositions
Definitions
- the invention relates to the use of certain alkyl polyglycol ether mixed formals as anti-foaming agents in strongly alkaline cleaning agents.
- Industrial cleaning agents in particular those used in automatic systems for cleaning rigid surfaces such as metal, ceramic or glass, and in particular for bottle cleaning, should have a low level of foaming with a strong cleaning power.
- the industrial cleaning agents of the type mentioned are mostly products which contain strongly alkaline substances, such as, in particular, alkali metal hydroxides or also alkali metal silicates or alkali metal orthophosphates, individually or in a mixture. In the case of such products, high demands are placed on the defoamers not only with regard to the anti-foam effect but also with regard to the storage stability in the corresponding solid products.
- the storage stability is not always sufficient in the case of packaging, for example in solid cleaning agents which contain a very high alkali content, in particular more than 50% and more caustic alkali. It is also desirable that the anti-foaming agents have good biodegradability, are alkali-stable, so that they do not lose their effectiveness during the cleaning process under constant exposure to temperature.
- alkyl polyglycol ether mixed formals of the formula are used as anti-foaming agents in alkaline cleaning agents in which R is a straight-chain or branched alkyl or alkylene radical having 8 to 22 carbon atoms, R 2 is a straight-chain or branched alkyl radical having 1 to 5 carbon atoms, m is a number from 2 to 30 and n is a number from 1 to 3.
- R 1 is an alkyl radical having 12 to 18 carbon atoms
- R 2 is an alkyl radical having 2 to 4 carbon atoms
- m is an integer from 7 to 15
- n is 1.
- the alkyl polyglycol ether mixed formals of the formula given above which are used can be prepared, for example by reaction of fatty alcohol ethoxylate of the formula with a di-alkyl glycol formal of the formula in the presence of a strong acid, such as sulfuric acid, by heating to temperatures of about 150 ° C. for several hours.
- R 1 and R 2 have the same meaning as given in formula I.
- Suitable starting products for the fatty alcohol ethoxylates are straight-chain or branched aliphatic alcohols, such as hexadecyl, tetradecyl and octadecyl alcohols, and the corresponding branched iso alcohols.
- Branched aliphatic alcohols which can be prepared by the so-called Guerbet reaction (dimerization of primary alcohols) can also be used.
- synthetic fatty alcohols or mixtures thereof, such as those obtained in oxo synthesis can also be used.
- the strongly alkaline cleaning agents (pH above 10) contain sodium or potassium hydroxide in particular.
- other strongly alkaline substances such as alkali carbonate and alkali orthophosphates, are used alone or in a mixture with alkali hydroxides.
- the alkaline cleaning agents can also contain the usual constituents, such as alkali silicates, alkali borates, polymeric alkali phosphates and / or complexing agents, such as phosphonic acids, in particular 1-hydroxyethane-1,1-diphosphonic acid, aminotrimethylenephosphonic acid or 2-phosphonobutane-1, 2,4-tricarboxylic acid.
- the molar ratio of Na 2 0 or K 2 0: P 2 0 5 can be 1: 1 to 2: 1.
- sodium tripolyphosphate is used.
- Finely divided synthetically produced, water-insoluble, bound water-containing aluminosilicates of the general formula can also be used as substitutes for the polyphosphates in the cat a cation of valence n, preferably sodium, exchangeable for calcium, x a number from 0.7 to 1.5, preferably 0.9 to 1.3, and y a number from 0.8 to 6, preferably of 1 , 3 to 4, which have a calcium binding capacity of 50 to 200, preferably 100 to 200 mg CaO / g of the anhydrous aluminosilicate can be used.
- aluminosilicates can be crystalline or X-ray amorphous.
- the crystalline sodium aluminosilicates are preferred, in particular the zeolites A and X.
- alkali stable anionic surfactants such as alkyl and / or aryl sulfonates, are also suitable as constituents.
- the amount of antifoam added is about 0.1 to 1 g / l, based on the solution used. The amount added depends on the desired antifoam effect and the impurities or bath concentration of the cleaning agent.
- the cleaning agents are generally used with a bath concentration of 0.2 to 10% depending on the intended use.
- the application temperature is generally between 40 and 90 ° C.
- the cleaning agents prepared in this way were each stored in closed polypropylene containers at 45 ° C. and the defoamer tests were carried out at intervals of 2 weeks each.
- the free fall cycle method consists in heating 500 ml of cleaning solution to 60 ° C in a jacketed 2-1 measuring cylinder.
- this solution is brought into constant circulation at a throughput capacity of 4 l / minute so that the solution is sucked from the bottom of the measuring cylinder with a glass tube and in the second via a second glass tube with the 2000 ml mark of the measuring cylinder free fall is returned.
- a constant initial foam volume (for example 2,000 ml) is established.
- composition of the cleaning agents specified under a was used. Comparable results were obtained with the cleaning agents of composition b.
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)
- Degasification And Air Bubble Elimination (AREA)
- Polyurethanes Or Polyureas (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT81103326T ATE5328T1 (de) | 1980-05-12 | 1981-05-02 | Verwendung von alkylpolyglykolethermischformale zur schaumverhuetung. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3018149 | 1980-05-12 | ||
DE19803018149 DE3018149A1 (de) | 1980-05-12 | 1980-05-12 | Verwendung von alkylpolyglykolethermischformale zur schaumverhuetung |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0040713A1 EP0040713A1 (de) | 1981-12-02 |
EP0040713B1 true EP0040713B1 (de) | 1983-11-16 |
Family
ID=6102215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP81103326A Expired EP0040713B1 (de) | 1980-05-12 | 1981-05-02 | Verwendung von Alkylpolyglykolethermischformale zur Schaumverhütung |
Country Status (15)
Country | Link |
---|---|
US (1) | US4364777A (es) |
EP (1) | EP0040713B1 (es) |
JP (1) | JPS5715806A (es) |
AR (1) | AR223116A1 (es) |
AT (1) | ATE5328T1 (es) |
BR (1) | BR8102900A (es) |
CA (1) | CA1157736A (es) |
DE (2) | DE3018149A1 (es) |
DK (1) | DK166781A (es) |
ES (1) | ES8300018A1 (es) |
FI (1) | FI66900C (es) |
MX (1) | MX7094E (es) |
NO (1) | NO151244C (es) |
TR (1) | TR21341A (es) |
ZA (1) | ZA813128B (es) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3048641A1 (de) * | 1980-12-23 | 1982-07-15 | Hoechst Ag, 6000 Frankfurt | "tensidhaltiges gemisch zur reinigung harter oberflaechen" |
US4394273A (en) * | 1981-12-10 | 1983-07-19 | Nl Industries, Inc. | Defoamers for aqueous liquids containing soluble zinc salts |
DE3315951A1 (de) * | 1983-05-02 | 1984-11-08 | Henkel KGaA, 4000 Düsseldorf | Verwendung von polyglykolethern als schaumdrueckende zusaetze in schaumarmen reinigungsmitteln |
DE3338923C1 (de) * | 1983-10-27 | 1985-02-21 | Th. Goldschmidt Ag, 4300 Essen | Verwendung von Copolymerisaten von Polyoxyalkylenethern des Allyl- und/oder Methallylalkohols und Vinylestern als Dismulgatoren fuer Wasser enthaltendes Rohoel |
DE3345349A1 (de) * | 1983-12-15 | 1985-06-27 | Henkel KGaA, 4000 Düsseldorf | Verwendung von polyglykolethern als schaumdrueckende zusaetze in schaumarmen reinigungsmitteln |
DE3418523A1 (de) * | 1984-05-18 | 1985-11-21 | Basf Ag, 6700 Ludwigshafen | Endgruppenverschlossene fettalkoholalkoxylate fuer industrielle reinigungsprozesse, insbesondere fuer die flaschenwaesche und fuer die metallreinigung |
DE3641447A1 (de) * | 1986-12-04 | 1988-06-09 | Henkel Kgaa | Tensidmischungen als sammler fuer die flotation nichtsulfidischer erze |
SE462599B (sv) * | 1987-04-06 | 1990-07-23 | Berol Kemi Ab | Foerpackning som foerhindrar skumbildning, saett att framstaella saadan foerpackning samt skumdaempande medel |
KR960002629B1 (ko) * | 1987-06-25 | 1996-02-24 | 가오 가부시끼가이샤 | 금속 세정제 |
GB8906820D0 (en) * | 1989-03-23 | 1989-05-10 | Ici Plc | Novel chemical compounds and their use as low foam surfactants and antifoamingagents |
US5068444A (en) * | 1989-10-31 | 1991-11-26 | Texaco Chemical Company | Tetramines by amination of dialdehyde glycol adducts |
CH684933A5 (de) * | 1992-04-01 | 1995-02-15 | Ciba Geigy Ag | Schaumarme oberflächenaktive Verbindungen. |
US5399239A (en) * | 1992-12-18 | 1995-03-21 | Ceridian Corporation | Method of fabricating conductive structures on substrates |
AU2015213032B2 (en) * | 2014-01-30 | 2018-11-01 | Basf Se | Asymmetric formales and acetales as adjuvants for crop protection |
CN109607648A (zh) * | 2018-12-19 | 2019-04-12 | 宁波瑞凌新能源科技有限公司 | 一种辐射制冷式海水淡化装置 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2905719A (en) * | 1959-09-22 | Cxhzo | ||
CA656004A (en) * | 1963-01-15 | A. Bixler Dean | Detergent composition | |
US2905720A (en) * | 1957-09-24 | 1959-09-22 | Rohm & Haas | Surface-active acetals and formals |
US2905718A (en) * | 1957-09-24 | 1959-09-22 | Rohm & Haas | Surface-active acetals and formals |
US3048548A (en) * | 1959-05-26 | 1962-08-07 | Economics Lab | Defoaming detergent composition |
NL128174C (es) * | 1962-02-28 | |||
DE1225800B (de) * | 1964-01-11 | 1966-09-29 | Henkel & Cie Gmbh | Schaumarme Spuel- und Reinigungsmittel |
DE2523588C2 (de) * | 1975-05-28 | 1983-11-10 | Hoechst Ag, 6230 Frankfurt | Polyglykoläthermischformale und deren Verwendung als ätzalkalibeständige Netz-, Wasch- und Reinigungsmittel |
US4070298A (en) * | 1976-07-26 | 1978-01-24 | Olin Corporation | Defoaming detergent additive |
DE2812443C2 (de) | 1978-03-22 | 1982-12-02 | Hoechst Ag, 6000 Frankfurt | Polyglykoläthermischformale sowie deren Verwendung als Faserpräparationsmittel |
-
1980
- 1980-05-12 DE DE19803018149 patent/DE3018149A1/de not_active Withdrawn
-
1981
- 1981-04-13 DK DK166781A patent/DK166781A/da not_active IP Right Cessation
- 1981-04-13 FI FI811131A patent/FI66900C/fi not_active IP Right Cessation
- 1981-04-13 NO NO811284A patent/NO151244C/no unknown
- 1981-04-27 US US06/257,855 patent/US4364777A/en not_active Expired - Fee Related
- 1981-04-30 CA CA000376613A patent/CA1157736A/en not_active Expired
- 1981-05-02 EP EP81103326A patent/EP0040713B1/de not_active Expired
- 1981-05-02 AT AT81103326T patent/ATE5328T1/de not_active IP Right Cessation
- 1981-05-02 DE DE8181103326T patent/DE3161415D1/de not_active Expired
- 1981-05-08 MX MX819442U patent/MX7094E/es unknown
- 1981-05-11 ES ES502104A patent/ES8300018A1/es not_active Expired
- 1981-05-11 ZA ZA00813128A patent/ZA813128B/xx unknown
- 1981-05-11 BR BR8102900A patent/BR8102900A/pt unknown
- 1981-05-12 TR TR21341A patent/TR21341A/xx unknown
- 1981-05-12 JP JP7287381A patent/JPS5715806A/ja active Pending
- 1981-05-12 AR AR285290A patent/AR223116A1/es active
Also Published As
Publication number | Publication date |
---|---|
TR21341A (tr) | 1984-04-16 |
DK166781A (da) | 1981-11-13 |
NO151244C (no) | 1985-03-06 |
ES502104A0 (es) | 1982-10-01 |
FI811131L (fi) | 1981-11-13 |
BR8102900A (pt) | 1982-02-02 |
CA1157736A (en) | 1983-11-29 |
AR223116A1 (es) | 1981-07-15 |
US4364777A (en) | 1982-12-21 |
ATE5328T1 (de) | 1983-12-15 |
EP0040713A1 (de) | 1981-12-02 |
NO151244B (no) | 1984-11-26 |
ZA813128B (en) | 1982-05-26 |
MX7094E (es) | 1987-06-08 |
DE3161415D1 (en) | 1983-12-22 |
JPS5715806A (en) | 1982-01-27 |
DE3018149A1 (de) | 1981-11-19 |
NO811284L (no) | 1981-11-13 |
ES8300018A1 (es) | 1982-10-01 |
FI66900B (fi) | 1984-08-31 |
FI66900C (fi) | 1984-12-10 |
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