EP2978833A1 - Fabric softener - Google Patents

Fabric softener

Info

Publication number
EP2978833A1
EP2978833A1 EP14712299.8A EP14712299A EP2978833A1 EP 2978833 A1 EP2978833 A1 EP 2978833A1 EP 14712299 A EP14712299 A EP 14712299A EP 2978833 A1 EP2978833 A1 EP 2978833A1
Authority
EP
European Patent Office
Prior art keywords
softening composition
fabric
alcohol
composition according
acid
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.)
Granted
Application number
EP14712299.8A
Other languages
German (de)
French (fr)
Other versions
EP2978833B1 (en
Inventor
Lin He
Hai Zhou ZHANG
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.)
Specialty Operations France SAS
Original Assignee
Rhodia Operations SAS
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=54867431&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2978833(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from PCT/EP2013/056228 external-priority patent/WO2014154234A1/en
Application filed by Rhodia Operations SAS filed Critical Rhodia Operations SAS
Priority to EP14712299.8A priority Critical patent/EP2978833B1/en
Publication of EP2978833A1 publication Critical patent/EP2978833A1/en
Application granted granted Critical
Publication of EP2978833B1 publication Critical patent/EP2978833B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/90Betaines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • C11D3/2013Monohydric alcohols linear fatty or with at least 8 carbon atoms in the alkyl chain
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2079Monocarboxylic acids-salts thereof

Definitions

  • the present invention concerns the use of Ci 6 -alkyl betaine as a fabric softener, notably for fabric softening compositions.
  • the invention also concerns a method of treating fabric which comprises the step of contacting said fabric in the rinse cycle of a fabric washing machine with an aqueous medium containing a composition as defined herein.
  • Fabric care compositions deliver a number of desirable characteristics to fabrics upon treatment, including an improved fabric feel and a perception of freshness.
  • it is essential to provide consumer-desirable product aesthetics, for example not only an appealing neat product odor and a pleasant product color, but especially an appropriate product rheology and satisfactory physical product stability.
  • Preferred fabric softener actives according to WO-A-02072745 are esterquats such as N,N-bis(stearoyl-oxy-ethyl) N,N-dimethyl ammonium chloride, N,N- bis(tallowoyl-oxy-ethyl) ⁇ , ⁇ -dimethyl ammonium chloride, N,N- bis(stearoyl-oxy-ethyl) N-(2-hydroxyethyl) N-methyl ammonium methylsulfate or l,2-di(stearoyl-oxy)-3-trimethyl ammoniumpropane chloride.
  • esterquats such as N,N-bis(stearoyl-oxy-ethyl) N,N-dimethyl ammonium chloride, N,N- bis(tallowoyl-oxy-ethyl) ⁇ , ⁇ -dimethyl ammonium chloride, N,N- bis(stearoyl-oxy-ethyl) N-(2-
  • the present invention is based on the surprising discovery that it is possible to obtain a stable fabric softener composition that performs well on softening fabrics, which comprises a fatty alkyl betaine.
  • Softening composition of the present invention comprising softener and water also provide the advantage to be homogeneous without phase separation.
  • the present invention then concerns a softening composition
  • the present invention also concerns the use of a compound of formula (I) as a fabric softener, notably for fabric softening compositions.
  • a fabric softener, or mixtures thereof, is an essential ingredient of the invention.
  • Typical levels of the fabric softener within the softening compositions are 0.1% to 20% by weight, preferably from 1% to 15% by weight, more preferably from 3 to 10% by weight.
  • Alkyl as used herein means a straight chain or branched saturated aliphatic hydrocarbon. Alkyl chain may notably comprise one or several heteroatoms such as N or O. In complex structures, the chains may be branched, bridged, or cross-linked.
  • the compound of formula (I) is cetyl betaine.
  • the softening composition may also comprise a Ci 0 -C 2 2 carboxylic acid and/or a Ci 0 -C 22 alcohol.
  • the Ci 0 -C 22 carboxylic acids are chosen on the group consisting of capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid and behenic acid.
  • the Ci 0 -C 22 alcohols are chosen on the group consisting of capryl alcohol, lauryl alcohol, myrityl alcohol, palmityl alcohol, stearyl alcohol, arachidyl alcohol and behenyl alcohol.
  • Weight ratio of compound of formula (I) to the Ci 0 -C 22 carboxylic acids and/or the Ci 0 -C 22 alcohols may be comprised between 4: 1 and 50: 1 , preferably between 10: 1 and 20: 1.
  • the neat pH, measured at 20C may be in the range of from 3 to 7.
  • the pH of these compositions herein can be regulated by the addition of acids such as Bronsted or Lewis ones.
  • suitable acids include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight (C C 5 )-carboxylic acids, and alkylsulfonic acids.
  • suitable inorganic acids include HCl, H 2 S0 4 , HN0 3 and H 3 P0 4 .
  • Suitable organic acids include formic, acetic, citric, methylsulfonic and ethylsulfonic acid.
  • Preferred acids are citric, hydrochloric, phosphoric, formic, methylsulfonic acid, and benzoic acids. Especially preferred is citric acid.
  • the softening composition may also comprise other fabric softeners classically used, such as for example quaternary ammonium salts, particularly dialkyl quats or ester quats.
  • Fabric softeners tend to be based on quaternary ammonium salts with one or two long alkyl chains, a typical compound being dipalmitoylethyl hydroxyethylmonium methosulfate.
  • Other cationic compounds can be derived from imidazolium, substituted amine salts, or quaternary alkoxy ammonium salts.
  • DHTDMAC dihydrogenated tallow dimethyl ammonium chloride
  • DHTDMAC dihydrogenated tallow dimethyl ammonium chloride
  • Softeners that may be used in combination with the compound of formula (I) are preferably quaternary ammonium softeners such as :
  • TET Di(tallowcarboxyethyl)hydroxyethyl methyl ammonium methylsulfate
  • TEO Di(oleocarboxyethyl)hydroxyethyl methyl ammonium methylsulfate
  • TES Distearyl hydroxyethyl methyl ammonium methylsulfate
  • TEHT Di(hydrogenated tallow-carboxyethyl)hydroxyethyl methyl ammonium methylsulfate
  • TEP Di(palmiticcarboxyethyl)hydroxyethyl methyl ammonium methylsulfate
  • silicones such as silicones, amine oxides, anionic surfactants, such as lauryl ether sulphate or lauryl sulphate, sulphosuccinates, amphoteric surfactants, such as amphoacetate, nonionic surfactants such as polysorbate, polyglucoside derivatives, etc,
  • stabilising products such as salts of amines having a short chain, which are quaternised or non-quaternised, for example of triethanolamine, N- methyldiethanolamine, etc., and also non-ionic surfactants, such as ethoxylated fatty alcohols, ethoxylated fatty amines, polysorbate, and ethoxylated alkyl phenols; typically used at a level of from 0 to 15% by weight of the composition,
  • inorganic salts such as calcium chloride, magnesium chloride, calcium sulphate, sodium chloride, etc.
  • products which can be used to reduce viscosity in concentrated compositions such as compounds of the glycol type, such as, ethylene glycol, dipropylene glycol, polyglycols, etc.
  • thickening agents for diluted compositions for example, polymers derived from cellulose, guar gum, etc, d) components for adjusting the pH, which is preferably from 4 to 6, such as any type of inorganic and/or organic acid, for example hydrochloric, sulphuric, phosphoric, citric acid etc,
  • agents that improve soil release such as the known polymers or copolymers based on terephthalates, f) bactericidal preservative agents,
  • the fabric softener according to the invention may take a variety of physical forms including liquid, liquid-gel, paste-like, foam in either aqueous or nonaqueous form, powder, granular and tablet forms.
  • a preferred form of the composition is a liquid form, and in the form of an aqueous dispersion in water.
  • the composition may also be dispensed with dispensing means such as a sprayer or aerosol dispenser.
  • such a fabric softener When in a liquid form, such a fabric softener may contain from 0.1% to 20 % by weight of a fabric softening agent, in the case of standard (diluted) fabric softener but may contain higher levels from up to 30% or even 40% by weight in the case of very concentrated fabric softeners.
  • the composition will usually also contain water and other additives, which may provide the balance of the composition.
  • Suitable liquid carriers are selected from water, organic solvents and mixtures thereof.
  • the liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost, safety, and environmental compatibility. Mixtures of water and organic solvent may be used.
  • Preferred organic solvents are; monohydric alcohol, such as ethanol, propanol, iso-propanol or butanol; dihydric alcohol, such as glycol; trihydric alcohols, such as glycerol, and polyhydric (polyol) alcohols.
  • Liquid fabric softeners are customarily prepared by melting the softening ingredients and adding the melt to hot water, with agitation to disperse the water-insoluble ingredients.
  • the fabric softener according to the invention can be used in a so-called rinse process, where a fabric softener as defined above, is first diluted in an aqueous rinse bath solution.
  • the laundered fabrics which have been washed with a detergent liquor and optionally rinsed in a first inefficient rinse step are placed in the rinse solution with the diluted composition.
  • the fabric softener may also be incorporated into the aqueous bath once the fabrics have been immersed therein.
  • agitation is applied to the fabrics in the rinse bath solution causing the suds to collapse, and residual soils and surfactant is to be removed.
  • the fabrics can then be optionally wrung before drying.
  • a method for rinsing fabrics which comprises the steps of contacting fabrics, preferably previously washed in a detergent liquor, with a softening composition or a fabric softener according to the invention.
  • the subject-matter of the invention also includes the use of a fabric softener of the present invention to impart fabric softness to fabrics that have been washed in a high suds detergent solution, while providing in the rinse a reduction of suds or foaming and without the creation of undesirable floes.
  • the present invention also concerns a method for softening a fabric comprising contacting a softening composition of the invention during a rinse cycle of a fabric washing machine with an aqueous medium comprising said softening composition.
  • This rinse process may be performed manually in basin or bucket, in a non- automated washing machine, or in an automated washing machine.
  • the laundered fabrics are removed from the detergent liquor and wrung out.
  • the fabric softener of the present invention may be then added to fresh water and the fabrics are then, directly or after an optional inefficient first rinse step, rinsed in the water containing the composition according to the conventional rinsing habit.
  • the fabrics are then dried using conventional means.
  • DHT Di(hydrogenated tallow) dimethyl ammonium chloride
  • Washing mode 1 main wash, 3 rinses, empty and 1 spin
  • Incline method Chinese National Standard Softener Evaluation Method GB/T 18318.1-2009 Textiles-determination of bending behavior-Part 1 : Incline method.
  • Sensorial test method revised ASTM D5237-05 standard guide for evaluating fabric softener. Blank was set as control with softness ranking of 0, which means the hardest. Another fabric was treated with another type of softener EAQ with softness ranking of 5 as a control, which means the softest.
  • OB or CB provides softness in comparison with compounds classically used in the softening compositions.
  • Softener treated fabric strips in certain size were stacked layer by layer.
  • a light weight (100. Og) and a heavy weight (550. Og) were applied on top of the stacked layer of strips and the height of the stack of strips is measured after 15 seconds as TlOOg and T550g respectively. The bigger the difference of the stack height under light and heavy weight, the more fluffy the fabric strip is.
  • Layer by layer method apparatus Layer number: 15 layers / Sample Size: 50 ⁇ lmm in width and 80 ⁇ lmm in length / Light weight: 100. Og weight standard / Heavy weight: 550. Og weight standard.
  • Formulation containing 5 % by weight of octadecyl diMe betaine visual observation of a suspension with particles that can not be dissolved. Even with a heating of formulation up to 55 C, formulation remains heterogeneous with part in the top.
  • Formulation containing 5 % by weight of octadecyl diMe betaine and 0.5 % of palmityl alcohol visual observation of a suspension with particles that can not be dissolved and a severe phase separation. Even with a heating of formulation up to 55 C, formulation remains heterogeneous with part in the top.

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)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The present invention concerns the use of C16-alkyl betaine as a fabric softener, notably for fabric softening compositions. The invention also concerns a method of treating fabric which comprises the step of contacting said fabric in the rinse cycle of a fabric washing machine with an aqueous medium containing a composition as defined herein.

Description

FABRIC SOFTENER
The present invention concerns the use of Ci6-alkyl betaine as a fabric softener, notably for fabric softening compositions. The invention also concerns a method of treating fabric which comprises the step of contacting said fabric in the rinse cycle of a fabric washing machine with an aqueous medium containing a composition as defined herein.
PRIOR ART
The following discussion of the prior art is provided to place the invention in an appropriate technical context and enable the advantages of it to be more fully understood. It should be appreciated, however, that any discussion of the prior art throughout the specification should not be considered as an express or implied admission that such prior art is widely known or forms part of common general knowledge in the field.
Fabric care compositions deliver a number of desirable characteristics to fabrics upon treatment, including an improved fabric feel and a perception of freshness. However, in order to secure high consumer acceptance of any fabric care composition, it is essential to provide consumer-desirable product aesthetics, for example not only an appealing neat product odor and a pleasant product color, but especially an appropriate product rheology and satisfactory physical product stability. Preferred fabric softener actives according to WO-A-02072745 are esterquats such as N,N-bis(stearoyl-oxy-ethyl) N,N-dimethyl ammonium chloride, N,N- bis(tallowoyl-oxy-ethyl) Ν,Ν-dimethyl ammonium chloride, N,N- bis(stearoyl-oxy-ethyl) N-(2-hydroxyethyl) N-methyl ammonium methylsulfate or l,2-di(stearoyl-oxy)-3-trimethyl ammoniumpropane chloride.
There is an abundant bibliography on the subject of combining dialkyl substituted quaternary ammonium compounds and monoalkyl quaternary ammonium compounds, amongst which patents or patent applications EP-A- 0018039, EP-A-0369500, U.S. Pat. No. 4,360,437 or U.S. Pat. No. 4,855,072 amongst many others, may be mentioned.
References describing mixtures of dialkyl substituted esterquats and monoalkyl esterquats are WO-A-9414935, WO-A-9742279, WO-A- 2004044113 amongst many others.
However, quats are known as very difficult to be biodegradable and provide confirmed eco toxicity, and it exists a general trend for this industry is to switch to esterquats, which provide better biodegradability and better eco toxicity. But even ester quats provides still some disavantages as a not so long term stability in the final product due to a degradability that imposes to keep a very low pH in order to make it more stable. Moreover, fabric turns to yellowish when they are treated repeatedly by ester quats. Ester quats are also known as cationic surfactants that can not be mixed directly with most of the anionic detergent system.
INVENTION
The present invention is based on the surprising discovery that it is possible to obtain a stable fabric softener composition that performs well on softening fabrics, which comprises a fatty alkyl betaine.
These compounds indeed appear to be sufficiently efficient and notably more efficient in term of softness, water absorbency and fluffmess, in comparison with the compounds classically used in the softening compositions such as di(palmiticcarboxyethyl) hydroxyethyl methyl ammonium methylsulfate (TEP), and Dimethyl di(hydrogenated tallow) ammonium chloride (DHT). These compounds also provide the advantages to be translucent and transparent, more stable over time and different pH range, and provide a good compatibility with all other surfactants system.
Softening composition of the present invention comprising softener and water also provide the advantage to be homogeneous without phase separation.
The present invention then concerns a softening composition comprising at least a fabric softener compound of formula (I):
R1-N (CH3)2-CH2-COO (I) wherein R1 is Ci6-alkyl.
The present invention also concerns the use of a compound of formula (I) as a fabric softener, notably for fabric softening compositions.
Other characteristics, details and advantages of the invention will emerge even more fully upon reading the description which follows.
Throughout the description, including the claims, the term "comprising one" should be understood as being synonymous with the term "comprising at least one", unless otherwise specified, and "between" should be understood as being inclusive of the limits.
A fabric softener, or mixtures thereof, is an essential ingredient of the invention. Typical levels of the fabric softener within the softening compositions are 0.1% to 20% by weight, preferably from 1% to 15% by weight, more preferably from 3 to 10% by weight.
"Alkyl" as used herein means a straight chain or branched saturated aliphatic hydrocarbon. Alkyl chain may notably comprise one or several heteroatoms such as N or O. In complex structures, the chains may be branched, bridged, or cross-linked.
In a preferred embodiment of the present invention, the compound of formula (I) is cetyl betaine. According to one embodiment of the present invention, the softening composition may also comprise a Ci0-C22 carboxylic acid and/or a Ci0-C22 alcohol.
Preferably, the Ci0-C22 carboxylic acids are chosen on the group consisting of capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid and behenic acid. Preferably, the Ci0-C22 alcohols are chosen on the group consisting of capryl alcohol, lauryl alcohol, myrityl alcohol, palmityl alcohol, stearyl alcohol, arachidyl alcohol and behenyl alcohol.
Weight ratio of compound of formula (I) to the Ci0-C22 carboxylic acids and/or the Ci0-C22 alcohols may be comprised between 4: 1 and 50: 1 , preferably between 10: 1 and 20: 1.
For optimum phase stability of these compositions, the neat pH, measured at 20C, may be in the range of from 3 to 7. The pH of these compositions herein can be regulated by the addition of acids such as Bronsted or Lewis ones. Examples of suitable acids include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight (C C5)-carboxylic acids, and alkylsulfonic acids. Suitable inorganic acids include HCl, H2S04, HN03 and H3P04. Suitable organic acids include formic, acetic, citric, methylsulfonic and ethylsulfonic acid. Preferred acids are citric, hydrochloric, phosphoric, formic, methylsulfonic acid, and benzoic acids. Especially preferred is citric acid.
The softening composition may also comprise other fabric softeners classically used, such as for example quaternary ammonium salts, particularly dialkyl quats or ester quats. Fabric softeners tend to be based on quaternary ammonium salts with one or two long alkyl chains, a typical compound being dipalmitoylethyl hydroxyethylmonium methosulfate. Other cationic compounds can be derived from imidazolium, substituted amine salts, or quaternary alkoxy ammonium salts. One of the most common compounds of the early formulations was dihydrogenated tallow dimethyl ammonium chloride (DHTDMAC). There are three main types of quaternary ammonium compounds used in the formulation of household fabric softeners: dialkyldimethyl ammonium compounds, diamido alkoxylated ammonium compounds, and imidazolinium compounds.
Softeners that may be used in combination with the compound of formula (I) are preferably quaternary ammonium softeners such as :
TET: Di(tallowcarboxyethyl)hydroxyethyl methyl ammonium methylsulfate TEO: Di(oleocarboxyethyl)hydroxyethyl methyl ammonium methylsulfate, TES : Distearyl hydroxyethyl methyl ammonium methylsulfate,
TEHT: Di(hydrogenated tallow-carboxyethyl)hydroxyethyl methyl ammonium methylsulfate, and
TEP: Di(palmiticcarboxyethyl)hydroxyethyl methyl ammonium methylsulfate In referring to other optional components, without this having to be regarded as an exhaustive description of all possibilities, which, on the other hand, are well known to the person skilled in the art, the following may be mentioned: a) other products that enhance the performance of the softening compositions, such as silicones, amine oxides, anionic surfactants, such as lauryl ether sulphate or lauryl sulphate, sulphosuccinates, amphoteric surfactants, such as amphoacetate, nonionic surfactants such as polysorbate, polyglucoside derivatives, etc,
b) stabilising products, such as salts of amines having a short chain, which are quaternised or non-quaternised, for example of triethanolamine, N- methyldiethanolamine, etc., and also non-ionic surfactants, such as ethoxylated fatty alcohols, ethoxylated fatty amines, polysorbate, and ethoxylated alkyl phenols; typically used at a level of from 0 to 15% by weight of the composition,
c) products that improve viscosity control, for example inorganic salts, such as calcium chloride, magnesium chloride, calcium sulphate, sodium chloride, etc.; products which can be used to reduce viscosity in concentrated compositions, such as compounds of the glycol type, such as, ethylene glycol, dipropylene glycol, polyglycols, etc.; and thickening agents for diluted compositions, for example, polymers derived from cellulose, guar gum, etc, d) components for adjusting the pH, which is preferably from 4 to 6, such as any type of inorganic and/or organic acid, for example hydrochloric, sulphuric, phosphoric, citric acid etc,
e) agents that improve soil release, such as the known polymers or copolymers based on terephthalates, f) bactericidal preservative agents,
g) other products such as antioxidants, colouring agents, perfumes, germicides, fungicides, anti-corrosive agents, anti-crease agents, opacifiers, optical brighteners, pearl lustre agents, etc.
The fabric softener according to the invention, may take a variety of physical forms including liquid, liquid-gel, paste-like, foam in either aqueous or nonaqueous form, powder, granular and tablet forms. For better dispersability, a preferred form of the composition is a liquid form, and in the form of an aqueous dispersion in water. When in a liquid form, the composition may also be dispensed with dispensing means such as a sprayer or aerosol dispenser.
When in a liquid form, such a fabric softener may contain from 0.1% to 20 % by weight of a fabric softening agent, in the case of standard (diluted) fabric softener but may contain higher levels from up to 30% or even 40% by weight in the case of very concentrated fabric softeners. The composition will usually also contain water and other additives, which may provide the balance of the composition. Suitable liquid carriers are selected from water, organic solvents and mixtures thereof. The liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost, safety, and environmental compatibility. Mixtures of water and organic solvent may be used. Preferred organic solvents are; monohydric alcohol, such as ethanol, propanol, iso-propanol or butanol; dihydric alcohol, such as glycol; trihydric alcohols, such as glycerol, and polyhydric (polyol) alcohols. Liquid fabric softeners are customarily prepared by melting the softening ingredients and adding the melt to hot water, with agitation to disperse the water-insoluble ingredients. The fabric softener according to the invention can be used in a so-called rinse process, where a fabric softener as defined above, is first diluted in an aqueous rinse bath solution. Subsequently, the laundered fabrics which have been washed with a detergent liquor and optionally rinsed in a first inefficient rinse step ("inefficient" in the sense that residual detergent and/or soil may be carried over with the fabrics), are placed in the rinse solution with the diluted composition. Of course, the fabric softener may also be incorporated into the aqueous bath once the fabrics have been immersed therein. Following that step, agitation is applied to the fabrics in the rinse bath solution causing the suds to collapse, and residual soils and surfactant is to be removed. The fabrics can then be optionally wrung before drying.
Accordingly, there is provided a method for rinsing fabrics, which comprises the steps of contacting fabrics, preferably previously washed in a detergent liquor, with a softening composition or a fabric softener according to the invention. The subject-matter of the invention also includes the use of a fabric softener of the present invention to impart fabric softness to fabrics that have been washed in a high suds detergent solution, while providing in the rinse a reduction of suds or foaming and without the creation of undesirable floes. The present invention also concerns a method for softening a fabric comprising contacting a softening composition of the invention during a rinse cycle of a fabric washing machine with an aqueous medium comprising said softening composition.
This rinse process may be performed manually in basin or bucket, in a non- automated washing machine, or in an automated washing machine. When hand washing is performed, the laundered fabrics are removed from the detergent liquor and wrung out. The fabric softener of the present invention may be then added to fresh water and the fabrics are then, directly or after an optional inefficient first rinse step, rinsed in the water containing the composition according to the conventional rinsing habit. The fabrics are then dried using conventional means. The invention is further illustrated in the following non limiting examples.
EXPERIMENTAL PART
Material information:
Cetyl betaine (CB)
- Cocoamidopropyl dimethyl betaine (CAPB)
Di(hydrogenated tallow) dimethyl ammonium chloride (DHT)
Di(palmiticcarboxyethyl) hydroxyethyl methyl ammonium methylsulfate (TEP) Fabrics that are tested in the experimental part are the following: Broadcloth: 100 % cotton fiber content / woven / Used for rewet method for water absorbency study
Terry cloth: 100 % cotton fiber content / looped file construction / Used for all of the other evaluation methods
I. Pre treatment, drying and softener treatment Procedure:
1) Fabric pretreatment method
Washing machine model: ELBA EWF 625
Surfactant: SLS (28%active)
Dosage of detergent: lO.Og/10 pieces of cotton towel (0.6kg)
Washing mode: 1 main wash, 3 rinses, empty and 1 spin
Wash temperature: 25 C
2) Drying of fabric
All fabric will be hanging dried in humidity room (Temp @20±1.0°C and humidity @55±3%) for overnight to let fabric dry and equilibrate efficiently before further use.
3) Softener treatment
Dosage of softener: 1.0wt% Softener formulation (5.0 or other active%) in 150ppm hard water
Soaking time: 30 min
Temperature: 25 C
Non-rinsing and hanging dry in humidity room II. Results and properties
1) Softness
Results for softness comparisons by incline method are mentioned in Table 1 , the shorter bending length, the better the softness.
Table 1
Incline method: Chinese National Standard Softener Evaluation Method GB/T 18318.1-2009 Textiles-determination of bending behavior-Part 1 : Incline method.
Results for influence from the additives to the softness effect tested by the incline method, the shorter bending length, the better the softness.
Table 1.1
When fatty acid or fatty alcohol is used as an additive for cetyl betaine, the softening effect is much improved, comparable or even better than TEP.
Results for softness comparisons by sensorial test method with 6 panelists are mentioned in Table 2.
Table 2
Sensorial test method: revised ASTM D5237-05 standard guide for evaluating fabric softener. Blank was set as control with softness ranking of 0, which means the hardest. Another fabric was treated with another type of softener EAQ with softness ranking of 5 as a control, which means the softest.
It appears then that OB or CB provides softness in comparison with compounds classically used in the softening compositions.
2) Water absorbency
Results for water absorbency are mentioned in Table 3.
Table 3
Water absorbency ability evaluation by Rewet method: revised ASTM D5237-05 standard guide for evaluating fabric softener It appears then that CB and OB provides equivalent or higher water absorbency ability in comparison with compounds classically used in the softening compositions.
3) Fluffiness evaluation
Results for fluffiness evaluation are mentioned in Table 4. Table 4
Softener treated fabric strips in certain size were stacked layer by layer. A light weight (100. Og) and a heavy weight (550. Og) were applied on top of the stacked layer of strips and the height of the stack of strips is measured after 15 seconds as TlOOg and T550g respectively. The bigger the difference of the stack height under light and heavy weight, the more fluffy the fabric strip is.
Fluffmess rating formulation:
Fluffiness%=(T100g-T550g)/T550g*100%
Layer by layer method apparatus: Layer number: 15 layers / Sample Size: 50±lmm in width and 80±lmm in length / Light weight: 100. Og weight standard / Heavy weight: 550. Og weight standard.
It appears then that CB provides equivalent or higher fluffmess ability in comparison with compounds classically used in the softening compositions. 4) Dissolution evaluation
4 formulations were made by addition of 5 % by weight of betaine compound and optionally 0.5 % by weight of palmityl alcohol in water. After keeping these formulations at room temperature, homogeneity of said formulations are expressed as follows:
A. Formulation containing 5 % by weight of cetyl betaine: full dissolution of cetyl betaine and visual observation of a homogeneous medium.
B. Formulation containing 5 % by weight of cetyl betaine and 0.5 % of palmityl alcohol: full dissolution of cetyl betaine and palmityl alcohol and visual observation of a homogeneous medium.
C. Formulation containing 5 % by weight of octadecyl diMe betaine: visual observation of a suspension with particles that can not be dissolved. Even with a heating of formulation up to 55 C, formulation remains heterogeneous with part in the top.
D. Formulation containing 5 % by weight of octadecyl diMe betaine and 0.5 % of palmityl alcohol: visual observation of a suspension with particles that can not be dissolved and a severe phase separation. Even with a heating of formulation up to 55 C, formulation remains heterogeneous with part in the top.

Claims

1. Softening composition comprising at least a fabric softener compound of formula (I):
R1-N (CH3)2-CH2-COO (I) wherein R1 is Ci6-alkyl.
2. Softening composition according to claim 1 wherein said composition comprises between 0.1% to 20% by weight of a fabric softener compound of formula (I).
3. Softening composition according to claim 1 or 2 wherein the compound of formula (I) is cetyl betaine.
4. Softening composition according to anyone of claims 1 to 3 wherein said softening composition comprises a Ci0-C22 carboxylic acid and/or a Ci0-C22 alcohol.
5. Softening composition according to claim 4 wherein the Ci0-C22 carboxylic acids are chosen on the group consisting of capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid and behenic acid.
6. Softening composition according to claim 4 wherein the Ci0-C22 alcohols are chosen on the group consisting of capryl alcohol, lauryl alcohol, myrityl alcohol, palmityl alcohol, stearyl alcohol, arachidyl alcohol and behenyl alcohol.
7. Softening composition according to anyone of claims 4 to 6 wherein the weight ratio of compound of formula (I) to the Ci0-C22 carboxylic acids and/or the Ci0-C22 alcohols is comprised between 4: 1 and 50: 1.
8. Softening composition according to anyone of claims 1 to 7 wherein the pH of the composition is in the range of from 3 to 7, measured at 20°C.
9. Method for rinsing fabrics, which comprises the steps of contacting fabrics, preferably previously washed in a detergent liquor, with a softening composition according to anyone of claims 1 to 8.
10. Method for softening a fabric comprising contacting a softening composition according to anyone of claims 1 to 8 during a rinse cycle of a fabric washing machine with an aqueous medium comprising said softening composition.
1 1. Use of a compound of formula (I) as a fabric softener, with
R1-N (CH3)2-CH2-COO (I) wherein R1 is Ci6-alkyl.
EP14712299.8A 2013-03-25 2014-03-25 Fabric softener Active EP2978833B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP14712299.8A EP2978833B1 (en) 2013-03-25 2014-03-25 Fabric softener

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
PCT/EP2013/056228 WO2014154234A1 (en) 2013-03-25 2013-03-25 Fabric softener
PCT/EP2014/055899 WO2014154654A1 (en) 2013-03-25 2014-03-25 Fabric softener
EP14712299.8A EP2978833B1 (en) 2013-03-25 2014-03-25 Fabric softener

Publications (2)

Publication Number Publication Date
EP2978833A1 true EP2978833A1 (en) 2016-02-03
EP2978833B1 EP2978833B1 (en) 2021-02-17

Family

ID=54867431

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14712299.8A Active EP2978833B1 (en) 2013-03-25 2014-03-25 Fabric softener

Country Status (1)

Country Link
EP (1) EP2978833B1 (en)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2172298B (en) 1985-03-01 1988-11-23 Procter & Gamble Mild detergent mousse
ES2217749T3 (en) 1998-05-20 2004-11-01 Kao Corporation SOFTENING FINISH COMPOSITION.
DE102004020015A1 (en) 2004-04-21 2005-11-10 Henkel Kgaa Textile Care
DE102004021732A1 (en) 2004-04-30 2005-11-24 Henkel Kgaa Textilplegemittel with amine group-containing cellulose ether
GB0611486D0 (en) 2006-06-09 2006-07-19 Unilever Plc Fabric softener composition
RU2552347C2 (en) 2010-12-09 2015-06-10 Колгейт-Палмолив Компани Liquid purifying composition, containing long-chain fatty acid

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2014154654A1 *

Also Published As

Publication number Publication date
EP2978833B1 (en) 2021-02-17

Similar Documents

Publication Publication Date Title
CN101600785B (en) No-rinse fabric softener
WO2015107155A1 (en) Method for stabilizing a softening composition
US10174273B2 (en) Fabric softener composition
ES2802407T3 (en) Active fabric softener compositions
EP2956532B1 (en) Fabric softener
US9714400B2 (en) Fabric softener
EP2978833B1 (en) Fabric softener
JP6671503B2 (en) Fabric softener active composition
ES2821398T3 (en) Active fabric softener compositions
ES2802425T3 (en) Active fabric softener compositions
MXPA98007977A (en) The use of a te softening composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20151026

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20180529

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: RHODIA OPERATIONS

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20200911

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602014074808

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1361472

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210315

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20210217

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210518

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210617

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210517

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210517

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1361472

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210217

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210617

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602014074808

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20210331

26 Opposition filed

Opponent name: HENKEL AG & CO. KGAA

Effective date: 20211111

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210325

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210325

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210331

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210331

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210617

RAP4 Party data changed (patent owner data changed or rights of a patent transferred)

Owner name: RHODIA OPERATIONS

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210331

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602014074808

Country of ref document: DE

Owner name: RHODIA OPERATIONS, FR

Free format text: FORMER OWNER: RHODIA OPERATIONS, AUBERVILLIERS, FR

Ref country code: DE

Ref legal event code: R081

Ref document number: 602014074808

Country of ref document: DE

Owner name: SPECIALTY OPERATIONS FRANCE, FR

Free format text: FORMER OWNER: RHODIA OPERATIONS, AUBERVILLIERS, FR

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20140325

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

REG Reference to a national code

Ref country code: DE

Ref legal event code: R100

Ref document number: 602014074808

Country of ref document: DE

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230624

R26 Opposition filed (corrected)

Opponent name: HENKEL AG & CO. KGAA

Effective date: 20211111

RAP2 Party data changed (patent owner data changed or rights of a patent transferred)

Owner name: SPECIALTY OPERATIONS FRANCE

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 20230704

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20240222 AND 20240228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602014074808

Country of ref document: DE

Owner name: SPECIALTY OPERATIONS FRANCE, FR

Free format text: FORMER OWNER: RHODIA OPERATIONS, LYON, FR

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210217

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20260202

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20260204

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20260209

Year of fee payment: 13