EP0743360B1 - Agent liquide aqueux de nettoyage de surfaces textiles - Google Patents
Agent liquide aqueux de nettoyage de surfaces textiles Download PDFInfo
- Publication number
- EP0743360B1 EP0743360B1 EP96107466A EP96107466A EP0743360B1 EP 0743360 B1 EP0743360 B1 EP 0743360B1 EP 96107466 A EP96107466 A EP 96107466A EP 96107466 A EP96107466 A EP 96107466A EP 0743360 B1 EP0743360 B1 EP 0743360B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- water
- cleaning
- alkoxylates
- 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 - Lifetime
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
- C11D3/43—Solvents
-
- 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
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0017—Multi-phase liquid compositions
- C11D17/0021—Aqueous microemulsions
-
- 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
- C11D3/0031—Carpet, upholstery, fur or leather cleansers
-
- 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
- C11D3/18—Hydrocarbons
Definitions
- the present invention relates to a liquid water-based cleaning agent of textile surfaces, which contains surfactants and organic solvents.
- the emulsions stand out for their organic content with water immiscible solvents especially due to their cleaning effect lipophilic stains. An optimal cleaning effect of this However, medium can only be achieved if they are present as stable emulsions, what an exact match of the quantitative ratios of each Components required. Are the proportions such. B. by dilution changed with water, it breaks up into a 2-phase system.
- the cleaning agents present as an emulsion are usually so-called stain removers or pre-treatment agents. Because of that contained in water-immiscible solvents, these agents stand out u. a. with a good cleaning effect on lipophilic soiling. However, as already described above, it is not possible to dilute these agents that they can also be used for large-scale carpet cleaning in conventional spray extraction processes or can be used in carpet pad processes because the Break up emulsions into 2-phase systems.
- Another disadvantage of the commercially available emulsions is that for their preparation, the mixtures of the individual components that are used for the production of the emulsions are necessary to be warmed because of their phase inversion temperature are above room temperature. Warming is especially low boiling ingredients problematic because they can easily escape.
- the present invention has for its object a cleaning agent for To provide textile surfaces that are available as an emulsion and any can be thinned without breaking the emulsion, in order to meet the requirements for universal use Carpet and upholstery cleaning. Another job is to provide a means that at the lowest possible temperatures can be produced so that even low-boiling ingredients without special precautions or safety measures can be incorporated.
- the agent according to the invention is a forms stable microemulsion, which can be diluted with water as desired, without in one break up multi-phase system.
- the agent according to the invention can be in concentrated form or in dilution as a stain remover, as a pretreatment agent for carpet cleaning, in the carpet pad process or use in the classic spray extraction process.
- Another object of the present invention is the use of the above described after dilution with water in one Ratio of 1:10 to 1:50 for carpet cleaning using the Spray extraction process.
- the diluted agent is spread over a large area cleaning substrate applied and after the exposure time again removed, the application and removal of the agent usually with the same device can be performed.
- Yet another object of the present invention is the use of the Agent described above in concentrated form or after dilution with water in a ratio up to 1:10 when cleaning carpets using the Carpet pad process.
- the agent is based on what is to be cleaned Substrate applied, usually sprayed on, and after an exposure time removed with a textile pad. To remove the agent, use usually uses a single-disc machine with a textile pad underneath is.
- the agent according to the invention is in the form of a microemulsion.
- the phase inversion temperature the agent is usually below room temperature, so that it can be produced at room temperature.
- the invention Means by combining the individual components and stirring the obtained Mixture prepared at room temperature.
- the agent so produced shows usually a transmission of 50 to 95%.
- the particle size is in the Rule below 120 nm.
- the agent obtained can be diluted with water as desired as a concentrate or diluted to a concentration of up to 0.5% by weight as a stable Microemulsion can be used.
- the agent according to the invention contains a surfactant mixture of C 12 -C 22 alcohol alkoxylates with a degree of alkoxylation below 8 and C 9 -C 15 oxo alcohol alkoxylates with a degree of alkoxylation of at least 10.
- the C 12 -C 22 alcohol alkoxylates are nonionic surfactants with the formulas I or II R 1 O- (CH 2 CH 2 O) m -H in which R 1 represents a saturated or unsaturated primary C 12 -C 22 alkyl group and m represents numbers from 1 to below 8, wherein R 2 and o can have the same meaning as R 1 and m in formula I and n stands for numbers from 0.5 to 2.
- the C 12 -C 22 alcohol alkoxylates can be obtained by alkoxylation of the primary C 12 -C 22 alcohols, in particular fatty alcohols with ethylene oxide (EO) and propylene oxide (PO).
- Suitable fatty alcohols are, for example, the native fatty alcohols based on plants, such as lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, oleyl alcohol, elaidyl alcohol, ricinol alcohol, linoleyl alcohol, linolenyl alcohol and mixtures thereof, such as coconut fatty alcohol, palm alcohol and palm kernel fat.
- C 12 -C 16 fatty alcohol ethoxylates are particularly preferably used.
- Oxoalcohol alkoxylates are also known compounds which can be obtained in a known manner by alkoxylating oxoalcohols.
- the oxo alcohols used are compounds made from petrochemical raw materials, e.g. B. can be obtained by Roelen's oxosynthesis.
- Particularly preferred oxo alcohol alkoxylates are the ethoxylates of C 11 -C 13 oxo alcohols with a degree of ethoxylation of more than 10.
- the alcohol alkoxylates and oxo alcohol alkoxylates are preferably used in a ratio of 1: 1 to 20: 1, particularly preferably from 5: 1 to 15: 1. Particularly stable microemulsions can be obtained in these mixing ratios.
- the agent according to the invention usually contains from 1 to 15% by weight, particularly preferably from 3 to 10% by weight, based in each case on the finished agent, of C 12 -C 22 fatty alcohol alkoxylates and from 0.5 to 5% by weight, preferably 0.1 to 1% by weight, in each case based on the finished agent, oxo alcohol alkoxylates.
- the agent according to the invention may further contain anionic surfactants as cleaning-active constituents.
- Suitable anionic surfactants are, for example, C 8 -C 18 alkyl sulfates, C 8 -C 18 alkyl ether sulfates, C 8 -C 18 alkane sulfates, C 8 -C 18 ⁇ -olefin sulfonates, sulfonated C 8 -C 18 fatty acids C 1 - C 4 alkyl esters, C 6 -C 18 alkylbenzenesulfonates, sulfosuccinic acid mono- and di-C 8 -C 12 alkyl esters, C 8 -C 18 alkyl polyglycol ether carboxylates, C 8 -C 18 -N-acyl taurides, C 8 -C 18 -N-Sarcosinate and C 8 -C 18 alkyl isethionates.
- the anionic surfactants can be present in amounts of up to 25% by weight, preferably 2.0 to 8.0 % By weight, based on the total agent, may be present.
- Suitable water-soluble organic solvents which can be used in the agent according to the invention are, in particular, lower alkyl alcohols, such as methanol, ethanol, isopropanol and butanol, or ethers of C 1 -C 4 -alcohols or phenol with (poly) glycols, such as, for example, phenoxyethanol, butyl glycol, propylene glycol -n-butyl ether, butyl diglycol and mixtures of the foregoing.
- the water-soluble organic solvents are present in an amount of 10 to 20% by weight, based on the finished agent.
- aliphatic hydrocarbons in an amount of 3 to 20 wt .-%, particularly preferably from 5 to 15 wt .-%, each based on the finished funds.
- Aliphatic hydrocarbons are particularly suitable with a chain length between 8 and 12 carbon atoms, the isoaliphatic Hydrocarbons are particularly preferred. Hydrocarbons with a Chain lengths below 8 carbon atoms should not be used as they are due to their low boiling point escape from the medium and for the cleaning process are not available. Chain length hydrocarbons over 12 carbon atoms are also not particularly preferred because Are solid at room temperature and are difficult to incorporate into the agents.
- the agent according to the invention contains polymers that delay or prevent new contamination of the cleaned substrate, so-called antisoiling agents.
- agents are in particular water-soluble, non-stick polymers with a film-forming temperature above 60 ° C, especially 80 to 100 ° C, preferred.
- Suitable polymers are (Meth) acrylic acid and (meth) acrylate homopolymers and copolymers.
- suitable polymers are commercially available as aqueous dispersions in which the polymers are generally present in a concentration of 30 to 40% by weight.
- the polymers are preferred in an amount of 0.4 to 10% by weight, especially preferably in an amount of 2 to 6% by weight, in each case based on the finished agent, used.
- the agents according to the invention can contain ammonia or alkaline agents as further ingredients Amines such as Monoethanolamine. These connections will be especially for adjusting the pH to a value between 8 and 10 added. A pH in this range is particularly preferred because the optional polymers remain clearly in solution at this pH and don't flocculate.
- the agent according to the invention can also contain other optional components Dyes and fragrances are added. These ingredients can be found in a lot up to 3% by weight, particularly preferably up to 1% by weight, based on the total Means to be included. Other auxiliaries customary in such agents can also be included, provided that they do not negatively affect the effect according to the invention influence.
- Example 1 Oleyl / cetyl alcohol with 5 EO 4.75% C 11 oxo alcohol with 11 EO 0.50% Isopropanol 15.00% Mixture of aliphatic C 10 -C 12 hydrocarbons (boiling range 155-200 ° C) 8.00% Polyacrylate dispersion (Ubatol® 1138; commercial product from Rivelli) 12.00% ammonia 0.20% water ad 100%
- Example 2 C 12 -C 14 fatty alcohol with 4 EO 4.00% C 13 oxo alcohol with 14 EO 0.70% Ethanol 12.00% Mixture of aliphatic C 8 -C 9 hydrocarbons (boiling range 140 - 165 ° C) 10.00% Polyacrylate dispersion (Ubatol® 1138; commercial product from Rivelli) 12.00% water ad 100%
- Example 3 C 16 -C 18 fatty alcohol ethoxylate with 7 EO 4.00% C 11 oxo alcohol with 11 EO 0.40% But
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)
Claims (7)
- Agent liquide aqueux de nettoyage de surfaces textiles, contenant des tensioactifs non ioniques et des solvants organiques, caractérisé en ce qu'il est présent sous la forme d'une microémulsion et qu'il renfermeA) 1 à 20 % en poids, par rapport à l'agent prêt à l'emploi, d'un mélange de surfactifs constitué d'alcoxylates d'alcools en C12-C22 présentant un degré d'alcoxylation inférieur à 8 et d'alcoxylates d'oxyalcools en C9-C15 possédant un degré d'alcoxylation d'au moins 10,B) B) 5 à 30 % en poids, par rapport à l'agent prêt à l'emploi, d'un solvant organique soluble dans l'eau etC) 3 à 20% en poids, par rapport à l'agent prêt à l'emploi, d'hydrocarbures aliphatiques.
- Agent selon la revendication 1, caractérisé en ce que les alcoxylates d'alcools en C12-C22 et les alcoxylates d'oxyalcools en C9-C15 sont mis en oeuvre dans un rapport de mélange de 1:1 à 20:1, de préférence de 5:1 à 15:1.
- Agent selon la revendication 1 ou 2, caractérisé en ce qu'il contient comme solvants solubles dans l'eau, des alcools alkyliques inférieurs et/ou des éthers d'alcools en C1-C4 ou de phénol avec des (poly)glycols, en particulier du phénoxyéthanol, du butylglycol, du propyléneglycol-n-butyléther, du butyldiglycol et des mélanges des composés qui précédent.
- Agent selon une des revendications 1 à 3, caractérisé en ce que l'on met en oeuvre comme hydrocarbures aliphatiques, des hydrocarbures comportant 8 à 12 atomes de carbone, en particulier des hydrocarbures isoaliphatiques.
- Agent selon une des revendications 1 à 4, caractérisé en ce qu'il renferme des polymères non collants, solubles dans l'eau, possédant une température de formation de films supérieure à 60 °C.
- Utilisation de l'agent de nettoyage de moquettes selon une des revendications 1 à 5, après dilution dans l'eau avec un taux de 1:10 à 1:50, pour le nettoyage des moquettes par le procédé d'extraction par aspersion.
- Utilisation de l'agent de nettoyage de moquettes selon une des revendications 1 à 5, sous forme concentrée ou après dilution dans l'eau avec un taux allant jusqu'à 1:10, pour le nettoyage des moquettes par le procédé dit du patin à moquette.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19517815A DE19517815A1 (de) | 1995-05-18 | 1995-05-18 | Flüssiges wasserhaltiges Mittel zur Reinigung von textilen Oberflächen |
DE19517815 | 1995-05-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0743360A1 EP0743360A1 (fr) | 1996-11-20 |
EP0743360B1 true EP0743360B1 (fr) | 2000-08-09 |
Family
ID=7761963
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP96107466A Expired - Lifetime EP0743360B1 (fr) | 1995-05-18 | 1996-05-10 | Agent liquide aqueux de nettoyage de surfaces textiles |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0743360B1 (fr) |
AT (1) | ATE195335T1 (fr) |
DE (2) | DE19517815A1 (fr) |
DK (1) | DK0743360T3 (fr) |
ES (1) | ES2150612T3 (fr) |
GR (1) | GR3034478T3 (fr) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998000497A2 (fr) * | 1996-06-28 | 1998-01-08 | Colgate-Palmolive Company | Composition liquide de nettoyage sous forme de microemulsion, d'usage general |
US7056874B2 (en) * | 2002-09-23 | 2006-06-06 | Ecolab Inc. | Cleaning solutions for carbon removal |
DE102009027206A1 (de) | 2009-06-25 | 2010-12-30 | Chemische Fabrik Kreussler & Co. Gmbh | Verwendung von Dietherverbindungen bei der chemischen Reinigung von Textil-, Leder- oder Pelzwaren |
US20120252713A1 (en) * | 2010-09-24 | 2012-10-04 | Invista North America S.A.R.L. | Composition for surface treatment and process |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1792066A1 (de) * | 1968-07-18 | 1971-10-14 | Henkel & Cie Gmbh | Schaumarmes Fleckenbehandlungsmittel fuer Textilien |
MY101656A (en) * | 1986-09-02 | 1991-12-31 | Colgate Palmolive Co | Laundry pre-spotter composition providing improved oily soil removal. |
EP0379544A1 (fr) * | 1988-06-21 | 1990-08-01 | Vax Appliances Limited | Compositions de nettoyage et d'assainissement de tissu |
NZ249441A (en) * | 1992-03-03 | 1995-12-21 | Reginald Keith Whiteley | Disinfectant composition containing an aqueous solution of tea tree oil |
-
1995
- 1995-05-18 DE DE19517815A patent/DE19517815A1/de not_active Withdrawn
-
1996
- 1996-05-10 AT AT96107466T patent/ATE195335T1/de not_active IP Right Cessation
- 1996-05-10 DK DK96107466T patent/DK0743360T3/da active
- 1996-05-10 ES ES96107466T patent/ES2150612T3/es not_active Expired - Lifetime
- 1996-05-10 DE DE59605697T patent/DE59605697D1/de not_active Expired - Lifetime
- 1996-05-10 EP EP96107466A patent/EP0743360B1/fr not_active Expired - Lifetime
-
2000
- 2000-09-26 GR GR20000402167T patent/GR3034478T3/el not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE59605697D1 (de) | 2000-09-14 |
EP0743360A1 (fr) | 1996-11-20 |
ATE195335T1 (de) | 2000-08-15 |
GR3034478T3 (en) | 2000-12-29 |
ES2150612T3 (es) | 2000-12-01 |
DK0743360T3 (da) | 2000-12-18 |
DE19517815A1 (de) | 1996-11-21 |
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