EP0011166B1 - Flüssiges, kältestabiles Waschmittelkonzentrat und seine Verwendung - Google Patents
Flüssiges, kältestabiles Waschmittelkonzentrat und seine Verwendung Download PDFInfo
- Publication number
- EP0011166B1 EP0011166B1 EP79104170A EP79104170A EP0011166B1 EP 0011166 B1 EP0011166 B1 EP 0011166B1 EP 79104170 A EP79104170 A EP 79104170A EP 79104170 A EP79104170 A EP 79104170A EP 0011166 B1 EP0011166 B1 EP 0011166B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- concentrate
- carbon atoms
- acid
- potassium
- 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- 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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/201—Monohydric alcohols linear
-
- 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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- 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
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
Definitions
- the subject of DE-OS 2 609 752 is a clear, cold-resistant detergent concentrate with a solids content of up to 55% by weight, containing 8 to 18% by weight of a potassium fatty acid soap, which is different from Derives fatty acids with 12 to 18 carbon atoms and consists predominantly of oleic acid, 10 to 25 wt .-% of ethoxylated alcohols with 8 to 12 carbon atoms and an average of 5 to 10 ethylene glycol ether groups and 4 to 10 wt .-% sodium alkylbenzenesulfonates with 10 to 14 carbon atoms in the Alkyl group, also optical brighteners and conventional solubilizers or water-miscible solvents.
- Means of this type are primarily intended for use in large laundry companies with automatically operated washing, drying and ironing machines, in which the individual work cycles overlap.
- the composition of a detergent suitable for this must be coordinated in such a way that there are no disturbances affecting the functioning of the machine or interrupting the work cycle. It has now been shown in certain modern washing machines that when using conventional detergents and to a certain - but to a lesser extent - even when using the agents according to DE-OS 2 609 752, the loading and unloading flaps running in grooves no longer have the necessary ease of movement and therefore no longer open and close according to the clock. Problems with spinning and hot ironing can also occur. For example, compacted laundry in self-centrifuging washing machines can only be detached from the drum wall with additional force, or problems can arise during transport and smoothing of the laundry on the mangling line.
- the potassium soaps listed under A) are derived from fatty acids of natural or synthetic origin, which consist of 60 to 100% by weight, preferably 65 to 95% by weight, of lauric acid, myristic acid or oleic acid. Mixtures of lauric acid and myristic acid should consist of at least half, preferably at least two thirds, of lauric acid.
- polyunsaturated fatty acids for example linoleic acid, can also be present in the fatty acids in proportions of 0 to 25, preferably 0.1 to 15% by weight.
- the proportion of saturated fatty acids with 16 to 18 carbon atoms is 0 to at most 20, preferably 1 to 15% by weight, the proportion of stearic acid expediently not to exceed 5% by weight and in particular 3% by weight.
- Suitable fatty acid mixtures have, for example, the following composition (in% by weight):
- composition II Agents based on composition II are particularly preferred.
- the ethoxylated alcohols listed under B) are derived from native or synthetic alcohols, in particular oxo alcohols having 8 to 14, preferably 9 to 12, carbon atoms.
- the oxo alcohols can be linearly branched or methyl-branched in the 2-position. Mixtures of native alcohols and alcohols obtained by oxo reaction are also suitable.
- the number of ethylene glycol ether groups is on average 5 to 10, preferably 6 to 8.
- the proportion of ethoxylated alcohols in the liquid concentrates should be 5 to 9, preferably 6 to 8% by weight.
- Component C) consists of linear sodium alkylbenzenesulfonate, in particular dodecylbenzenesulfonate, in proportions of 4 to 10, preferably 6 to 8,% by weight.
- Optical brighteners of the formula F are preferably used, in which R 1 and R 2 represent morpholino, diethanolamino or anilino residues.
- the optical brighteners are in proportions of 0.05 to 1, preferably from 0.1 to 0.7% by weight.
- Component D) serves to make the solution or the wash liquor alkaline.
- the amount of potassium hydroxide is preferably such that it exceeds the stoichiometric amount required to form the potassium fatty acid soaps by 10 to 50 mol percent, in particular by 20 to 35 mol percent.
- the triethanolamine (component F) improves the cold resistance of the concentrates and is present in amounts of up to 6% by weight, preferably 2 to 5% by weight.
- Component G) consists of aliphatic C 3 -C 3 alcohols, ie methanol, ethanol, propanol and in particular isopropanol, and of the mixtures of the alcohols mentioned.
- the content of these alcohols in the compositions is preferably 12 to 18% by weight.
- Agents with fractions of less than 12% of the alcohols mentioned can also contain hydrotropic ether alcohols derived from C 1 -C 4 monoalcohols or ethylene glycol or propylene glycol or diglycols, or hydrotropic alkylbenzenesulfonates with short alkyl chains.
- Suitable are, for example, the monomethyl, monoethyl, monopropyl, monoisopropyl or monobutyl ether of ethylene glycol and, from the group of the alkylbenzenesulfonates, the toluenesulfonate, ethylbenzenesulfonate, cumene sulfonate and xylene sulfonate in the form of the potassium or preferably sodium salts.
- the proportion of these solution-improving substances can be up to 5 ° / o.
- the water content of the detergent concentrate should not fall below 30% by weight. There are no limits in the direction of more dilution, but it is advisable not to exceed a water content of 55% in order to save on packaging and transport volume. In general, a water content of 30 to 50% by weight is sufficient to achieve optimal results, i.e. Such concentrates remain clear, even when stored for several weeks at a temperature of -10 ° C. and do not tend to solidify, gel or separate under such extreme conditions.
- additives may also include biocides, fragrances, dyes, stabilizers, sequestering agents, neutral salts and optical brighteners of other constitution, but the proportion of such additives should not total 10% by weight. exceed and preferably less than 5 wt .-%, in particular less than 2 wt .-%, so that a negative impact on the cold stability is avoided.
- the laundry detergents according to the invention are used in an amount of 3 to 10 g per kg of dry laundry, preferably using softened water. They are suitable as pre or main detergents for textiles of all kinds, e.g. those made of cellulose, synthetic and semi-synthetic fibers. Preferred areas of application are fully automatic washing, drying and ironing devices, as are customary in large commercial laundries.
- the agents can be added as washing-strengthening additives to washing liquors of conventional composition, ie those which, in addition to surfactants, also contain, for example, washing alkalis, phosphates, sequestering agents, bleaching agents and anti-graying substances.
- a liquid washing alkali concentrate which is particularly suitable for use in large automatic washing systems and with which the agent according to the invention can be combined when used has the following composition:
- the potassium soaps used in the recipes still had the following fatty acid composition (in% by weight):
- Component B An oxo alcohol of chain length C, -C " with 7 ethylene glycol ether groups was used as the ethoxylated alcohol (component B).
- Component C consisted of linear Na dodecyl benzenesulfonate.
- the sodium salt of the compound of the formula I in which R 1 and R 2 were morpholino radicals was used as the optical brightener (component D).
- Component G consisted of isopropanol.
- the component “salts” means small amounts of Na 2 SO 4 and NaCI which were present as accompanying substances of the alkylbenzenesulfonate and the optical brightener.
- the composition is shown in Table 2.
- the soap including the excess potassium hydroxide solution in the form of a 65% aqueous paste with the ethoxylate and. the alkylbenzenesulfonate, which was in the form of a 50% strength aqueous solution, mixed with one another, the optical brightener dissolved in isopropanol was then stirred in and finally triethanolamine and water were added to the stated amount.
- the concentrates were in the form of yellowish, clear solutions which had a low viscosity at room temperature and which remained clear and homogeneous when stored for three weeks in a climatic cabinet at -10 ° C and + 50 ° C. A multiple temperature change between + 50 ° and -10 ° C also did not change the appearance and behavior of the samples.
- the concentrates were miscible with water in all proportions.
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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT79104170T ATE975T1 (de) | 1978-11-02 | 1979-10-29 | Fluessiges, kaeltestabiles waschmittelkonzentrat und seine verwendung. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2847438 | 1978-11-02 | ||
DE19782847438 DE2847438A1 (de) | 1978-11-02 | 1978-11-02 | Fluessiges, kaeltestabiles waschmittelkonzentrat |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0011166A1 EP0011166A1 (de) | 1980-05-28 |
EP0011166B1 true EP0011166B1 (de) | 1982-05-05 |
Family
ID=6053620
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP79104170A Expired EP0011166B1 (de) | 1978-11-02 | 1979-10-29 | Flüssiges, kältestabiles Waschmittelkonzentrat und seine Verwendung |
Country Status (5)
Country | Link |
---|---|
US (1) | US4268262A (zh) |
EP (1) | EP0011166B1 (zh) |
AT (2) | ATE975T1 (zh) |
DE (1) | DE2847438A1 (zh) |
DK (1) | DK146341C (zh) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4310433A (en) | 1980-09-02 | 1982-01-12 | The Procter & Gamble Company | Superfatted liquid soap skin cleansing compositions |
JPS5910760B2 (ja) * | 1980-12-26 | 1984-03-10 | ダスキンフランチヤイズ株式会社 | 粘性のある液体石鹸組成物 |
IT1147874B (it) * | 1982-04-30 | 1986-11-26 | Colgate Palmolive Co | Procedimento di lavaggio industriale e composizione |
US4561998A (en) * | 1982-05-24 | 1985-12-31 | The Procter & Gamble Company | Near-neutral pH detergents containing anionic surfactant, cosurfactant and fatty acid |
US4507219A (en) * | 1983-08-12 | 1985-03-26 | The Proctor & Gamble Company | Stable liquid detergent compositions |
GB2187749B (en) * | 1986-03-11 | 1990-08-08 | Procter & Gamble | Stable liquid detergent composition hydrophobic brightener |
HUT64784A (en) * | 1990-09-28 | 1994-02-28 | Procter & Gamble | Detergent preparatives containijng n-(polyhydroxi-alkyl)-fatty acid amides and cleaning agents |
US5174927A (en) * | 1990-09-28 | 1992-12-29 | The Procter & Gamble Company | Process for preparing brightener-containing liquid detergent compositions with polyhydroxy fatty acid amines |
BR9106920A (pt) * | 1990-09-28 | 1993-08-17 | Procter & Gamble | Composicoes detergentes contendo tensoativos de amida de acido poliidroxi graxo e alquil ester sulfonato |
EP0550690B1 (en) * | 1990-09-28 | 1998-03-25 | The Procter & Gamble Company | Polyhydroxy fatty acid amide surfactants in bleach-containing detergent compositions |
US5254281A (en) * | 1991-01-29 | 1993-10-19 | The Procter & Gamble Company | Soap bars with polyhydroxy fatty acid amides |
US5589448A (en) * | 1993-02-17 | 1996-12-31 | The Clorox Company | High water liquid enzyme prewash composition |
US5789364A (en) * | 1993-02-17 | 1998-08-04 | The Clorox Company | High water liquid enzyme prewash composition |
US6376446B1 (en) | 1999-01-13 | 2002-04-23 | Melaleuca, Inc | Liquid detergent composition |
US6506714B1 (en) | 2000-10-31 | 2003-01-14 | Colgate-Palmolive Company | Method for stopping hysteresis |
DE102016210744A1 (de) * | 2016-06-16 | 2017-12-21 | Henkel Ag & Co. Kgaa | Konzentrierte Flüssigwaschmittel mit konstantem pH-Wert |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2097737A (en) * | 1935-08-10 | 1937-11-02 | Hercules Powder Co Ltd | Detergent composition |
US2792347A (en) * | 1953-10-30 | 1957-05-14 | Emery Industries Inc | Fatty acid mixtures and soaps derived therefrom |
CA767063A (en) * | 1964-11-25 | 1967-09-12 | Pelizza Carlo | Composition for an anchored-foam biodegredable liquid detergent for universal household and industrial use |
US4065398A (en) * | 1973-03-12 | 1977-12-27 | Lever Brothers Company | Liquid soap composition |
US4079078A (en) * | 1974-06-21 | 1978-03-14 | The Procter & Gamble Company | Liquid detergent compositions |
DE2635913A1 (de) * | 1975-08-13 | 1977-03-03 | Procter & Gamble Europ | Fluessiges waschmittel |
DE2609752A1 (de) * | 1976-03-09 | 1977-09-22 | Henkel & Cie Gmbh | Fluessiges, kaeltestabiles waschmittelkonzentrat |
US4058473A (en) * | 1976-06-24 | 1977-11-15 | Lever Brothers Company | Low temperature stable compositions |
-
1978
- 1978-11-02 DE DE19782847438 patent/DE2847438A1/de active Granted
-
1979
- 1979-10-05 DK DK419879A patent/DK146341C/da not_active IP Right Cessation
- 1979-10-19 US US06/086,478 patent/US4268262A/en not_active Expired - Lifetime
- 1979-10-29 EP EP79104170A patent/EP0011166B1/de not_active Expired
- 1979-10-29 AT AT79104170T patent/ATE975T1/de not_active IP Right Cessation
- 1979-10-31 AT AT0703679A patent/AT374823B/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DK146341C (da) | 1984-02-20 |
ATA703679A (de) | 1983-10-15 |
AT374823B (de) | 1984-06-12 |
ATE975T1 (de) | 1982-05-15 |
DK419879A (da) | 1980-05-03 |
DK146341B (da) | 1983-09-12 |
DE2847438A1 (de) | 1980-05-22 |
US4268262A (en) | 1981-05-19 |
EP0011166A1 (de) | 1980-05-28 |
DE2847438C2 (zh) | 1988-03-24 |
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