EP3201302B1 - Formule contenant des bio-tenseurs - Google Patents

Formule contenant des bio-tenseurs Download PDF

Info

Publication number
EP3201302B1
EP3201302B1 EP15760136.0A EP15760136A EP3201302B1 EP 3201302 B1 EP3201302 B1 EP 3201302B1 EP 15760136 A EP15760136 A EP 15760136A EP 3201302 B1 EP3201302 B1 EP 3201302B1
Authority
EP
European Patent Office
Prior art keywords
weight
component
formulation according
formulation
betaines
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.)
Active
Application number
EP15760136.0A
Other languages
German (de)
English (en)
Other versions
EP3201302A1 (fr
Inventor
Joerg Peggau
Ulrike Kottke
Hans Henning Wenk
Dirk Kuppert
Jochen Kleinen
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.)
Evonik Operations GmbH
Original Assignee
Evonik Degussa GmbH
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
Application filed by Evonik Degussa GmbH filed Critical Evonik Degussa GmbH
Publication of EP3201302A1 publication Critical patent/EP3201302A1/fr
Application granted granted Critical
Publication of EP3201302B1 publication Critical patent/EP3201302B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/94—Mixtures with anionic, cationic or non-ionic 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
    • C11D1/825—Mixtures of compounds all of which are non-ionic
    • 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
    • C11D1/83—Mixtures of non-ionic with anionic 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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/92—Sulfobetaines ; Sulfitobetaines
    • 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
    • C11D3/0094—High foaming compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/04—Carboxylic acids or salts thereof
    • C11D1/06—Ether- or thioether carboxylic acids
    • 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
    • C11D1/29—Sulfates of polyoxyalkylene 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
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/662—Carbohydrates or derivatives
    • 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
    • C11D1/667—Neutral esters, e.g. sorbitan esters
    • 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
    • C11D1/75—Amino oxides
    • 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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/886—Ampholytes containing P
    • 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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/90—Betaines

Definitions

  • the invention relates to biosurfactant formulations and their use as detergents with improved foaming and fat-dissolving power containing at least one further surfactant.
  • detergent compositions which can also be used as hand dishwashing detergents, usually contain combinations of surfactants in order to meet the demands of the consumer on the cleaning line and foaming.
  • the formulations must not only have a high rinsing power but also a pronounced foaming power and a fast foaming ability.
  • EP1445302 discloses detergent compositions comprising at least one glycolipid biosurfactant and at least one non-glycolipid surfactant, characterized in that the at least one glycolipid biosurfactant and the at least one non-glycolipid surfactant are in the micellar phase.
  • a reduced foam effect of the surfactants is achieved, whereby an advantageous use in washing machines is made possible.
  • EP14453021 are low-foam formulations. In particular, it is shown in the examples that the addition of Sophorolipden to the anionic surfactant sodium lauryl sulfate (SLS), leading to a reduction in foaming.
  • SLS sodium lauryl sulfate
  • the WO 2011/120776 describes a foaming detergent composition consisting of a) 1 to 20% by weight of sophorolipid biosurfactant, b) 1 to 20% of an anionic surfactant selected from the group comprising glycinates, sulfosuccinates and mixtures thereof, c) 0 to 10% by weight of a Foam booster, d) 0 to 2% by weight of an electrolyte, e) 0 to 10% by weight of additional additives and 40 to 98% of water.
  • Foambooster only Oliveamidopropylbetaine is mentioned, with no example or foaming power data are listed.
  • the US 5417879 discloses combinations of glycolipids and non-glycolypids surfactants for the removal of oil and dirt.
  • the preferred glycolipids are also called sophorolipids.
  • sophorolipids are in combination with nonionic surfactants.
  • the DE 19600743 describes combinations of glycolipids with a long list of anionic surfactants, nonionic surfactants and amphoteric surfactants. However, only examples of binary mixtures of a glycolipid with a non-glycolipid are listed. For Sophorolipde in particular, only examples of binary mixtures with sodium lauryl sulfate are listed as anionic surfactant.
  • the WO 2013/098066 is directed to a composition comprising water, at least one biosurfactant and at least one fatty acid, which is characterized in that the proportion of the sum of all surfactants in the composition of 1 to 30 wt -.%, and that the proportion of fatty acid based on the sum from fatty acid and surfactants from 0.1% to 20% by weight, and their use as or for the preparation of bath additives, shower gels, shampoos, conditioners, body cleansers or skin cleansers.
  • the object of the present invention was to provide formulations with a sophorolipid which have excellent foaming behavior.
  • the formulations should also have improved fat dissolving power, i. have an improved cleaning power.
  • Another object of the invention is the use of the formulations according to the invention for foam stabilization.
  • An advantage of the present invention is that the formulations foam strongly, i. create a large foam volume.
  • Another advantage of the present invention is that the formulations produce time stable foams.
  • Yet another advantage of the present invention is that the formulations have good foaming behavior.
  • Another advantage of the present invention is that the formulations have good skin tolerance.
  • Yet another advantage of the present invention is that the formulations have good drainage performance.
  • Another advantage of the present invention is that the formulations have a good drying behavior.
  • Another advantage of the present invention is that the formulations also exhibit excellent foaming power in the presence of oil soil.
  • Yet another advantage of the present invention is that it is possible to formulate high-foaming formulations prepared without the use of surfactants prepared with ethylene oxide, if in group B) only betaines, in particular from alkyl dimethyl betaines, alkyl amidopropyl betaines and alkyl amine oxides.
  • the formulations of the invention contain as component A) a biosurfactant selected from the group of sophorolipids, sophorolipids can be used according to the invention in their acid form or their lactone form.
  • a biosurfactant selected from the group of sophorolipids, sophorolipids can be used according to the invention in their acid form or their lactone form.
  • acid form of sophorolipids is based on the general formula (Ia) of EP2501813 refer to the term "lactone form” of sophorolipids is based on the general formula (Ib) of EP2501813 directed.
  • Preferred formulations according to the invention comprise, as component A), a sophorolipid in which the weight ratio of lactone form to acid form is in the range from 20:80 to 80:20, most preferably in the ranges from 30:70 to 40:60.
  • Preferred betaines are the alkylbetaines of the formula (Ia), the alkylamidobetaines of the formula (Ib), the sulfobetaines of the formula (Ic) and the amidosulfobetaines of the formula (Id), R 1 -N + (CH 3 ) 2 -CH 2 COO - (la) R 1 -CO-NH- (CH 2 ) 3 -N + (CH 3 ) 2 -CH 2 COO - (Ib) R 1 is -N + (CH 3 ) 2 -CH 2 CH (OH) CH 2 SO 3 - (Ic) R 1 -CO-NH- (CH 2 ) 3 -N + (CH 3 ) 2 -CH 2 CH (OH) CH 2 SO 3 - (Id) in which R 1
  • betaines are the carbo-betaines, in particular the carbo-betaines of the formula (Ia) and (Ib), most preferably the alkylamido-betaines of the formula (Ib).
  • betaines and sulfobetaines are the following compounds designated as INCI: almondamidopropyl betaines, apricotamidopropyl betaines, avocadamidopropyl betaines, babassuamidopropyl betaines, behenamidopropyl betaines, behenyl betaines, betaines, canolamidopropyl betaines, caprylic / capramidopropyl betaines, carnitines, cetyl betaines, cocamidoethyl betaines, cocamidopropyl Betaines, cocamidopropyl hydroxysultaines, coco-betaines, coco-hydroxysultaines, coco / oleamidopropyl betaines, coco-sultaines, decyl betaines, dihydroxyethyl, oleyl glycinates, dihydroxyethyl soy glycinates, dihydroxye
  • An especially preferred betaine is, for example, cocamidopropyl betaine (cocoamidopropylbetaine).
  • Alkoxylated fatty alcohol sulfates also alkyl ether sulfates, fatty alcohol ether sulfates or INCI alkyl ether sulfates are products of sulfation reactions on alkoxylated alcohols.
  • alkoxylated alcohols the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, in the context of the present invention preferably with longer chain alcohols, d. H.
  • alcohols having 6 to 22, preferably 8 to 18, in particular 10 to 16 and particularly preferably 12 to 14 carbon atoms.
  • n 1 to 30, preferably 1 to 20, especially 1 to 10, particularly preferably 2 to 4).
  • alkoxylation is the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide.
  • EO ethylene oxide units
  • 2 EO such as Na-C12-14-fatty alcohol + 2EO sulfate, commonly known as lauryl ether sulfate.
  • Suitable amine oxides include alkylamine oxides, especially alkyldimethylamine oxides, alkylamidoamine oxides, and alkoxyalkylamine oxides.
  • Preferred amine oxides satisfy formula II and III, R 6 R 7 R 8 N + -O - (II) R 6 - [CO-NH- (CH 2 ) w ] z -N + (R 7 ) (R 8 ) -O - (III) in the R 6 is a saturated or unsaturated C6-22-alkyl radical, preferably C8-18-alkyl radical, in particular a saturated C10-16-alkyl radical, for example a saturated C12-14-alkyl radical which in the Alkylamidoaminoxiden via a
  • R 7 , R 8 independently of one another a C 1-4 -alkyl radical, optionally hydroxy-substituted, such as. B. is a hydroxyethyl radical, in particular a methyl radical.
  • Suitable amine oxides are the following compounds designated as INCI: Almondamidopropylamine oxides, Babassuamidopropylamine oxides, Behenamine oxides, Cocamidopropyl Amine oxides, Cocamidopropylamine oxides, Cocamine oxides, Coco-Morpholine oxides, Decylamine oxides, Decyltetradecylamine oxides, Diaminopyrimidine oxides, Dihydroxyethyl C8-10 alkoxypropylamines oxides , Dihydroxyethyl C9-11 alkoxypropylamines oxides, dihydroxyethyl C12-15 alkoxypropylamines oxides, dihydroxyethyl cocamine oxides, dihydroxyethyl lauramine oxides, dihydroxyethyl stearamines oxides, dihydroxyethyl tallowamine oxides, hydrogenated palm kernel amine oxides, hydrogenated tallowamine oxides, hydroxyethyl hydroxypropyl C
  • Formulations according to the invention additionally comprise C) at least one fatty acid.
  • the at least one fatty acid in the compositions according to the invention is selected from the group dimeric ⁇ -hydroxy-decanoic acid, oleic acid, palmitic acid, stearic acid and / or linoleic acid. Very particular preference is oleic acid.
  • the formulations according to the invention are characterized in that the weight ratio of sophorolipid in the lactone form to component C), in particular oleic acid, is between 50: 1 and 80: 1.
  • Very particularly preferred formulations according to the invention comprise, as component A), a sophorolipid in which the weight ratio of lactone form to acid form is in the range from 20:80 to 80:20, very particularly preferably in the ranges from 30:70 to 40:60, and the weight ratio of sophorolipid in lactone form to component C), which is oleic acid, is between 50: 1 to 80: 1.
  • the pH of the formulations according to the invention can be adjusted by means of customary pH regulators, for example acids such as mineral acids or citric acid and / or alkalis such as sodium or potassium hydroxide, a range from 3 to 11, preferably 4 to 9, in particular 5 to 8 and most preferably 5.5 to 7.5, the pH being determined at 25 ° C.
  • acids such as mineral acids or citric acid and / or alkalis such as sodium or potassium hydroxide
  • the formulation may contain one or more buffer substances (INCI Buffering Agents), usually in amounts of 0.001 to 5 wt .-%, preferably 0.005 to 3 wt .-%, in particular 0, 01 to 2 wt .-%, particularly preferably 0.05 to 1 wt .-%, most preferably 0.1 to 0.5 wt .-%, for example, 0.2 wt .-%.
  • buffer substances which are at the same time complexing agents or even chelating agents (INCI chelating agents).
  • Particularly preferred buffer substances are the citric acid or the citrates, in particular the sodium and potassium citrates, for example trisodium citrate.2H 2 O and tripotassium citrate H 2 O.
  • Preferred formulations according to the invention comprise as component B) an additional surfactant selected from the group cocamidopropylbetaine, ethoxylated lauryl ether sulfates, in particular ethoxylated with 1 to 4 EO, cocamidopropylamine oxide and cocoamine oxide.
  • an additional surfactant selected from the group cocamidopropylbetaine, ethoxylated lauryl ether sulfates, in particular ethoxylated with 1 to 4 EO, cocamidopropylamine oxide and cocoamine oxide.
  • compositions according to the invention comprise as component A) a sophorolipid and as component B) an additional surfactant selected from the group cocamidopropylbetaine, with 1 to 4 EO ethoxylated lauryl ether sulfate, cocamidopropylamine oxide and cocoamine oxide.
  • Very particularly preferred formulations according to the invention comprise as component A) a sophorolipid and as component B) the additional surfactants cocamidopropylbetaine and lauryl ether sulphate ethoxylated with 1 to 4EO, the weight ratio of component A) sophorolipid to component B) cocamidopropylbetaine and lauryl ether sulphate ethoxylated with 1 to 4 EO preferably in a range from 5:95 to 95: 5, preferably from 15:85 to 75:25, and most preferably from 30:70 to 50:50.
  • Formulations according to the invention comprise component A), preferably in a concentration of from 0.01% by weight to 95% by weight, preferably from 0.1% by weight to 40% by weight, particularly preferably from 1% by weight 20 wt .-%, wherein the percentages by weight relate to the total formulation.
  • Formulations according to the invention comprise component B) preferably in a concentration of from 0.01% by weight to 95% by weight, preferably from 0.1% by weight to 50% by weight, particularly preferably from 1% by weight to 30% by weight, the weight percentages being based on the total formulation
  • the weight ratio of component A) to component B) in the formulation according to the invention is from 5:95 to 95: 5, preferably from 15:85 to 75:25 and most preferably from 30:70 to 50:50.
  • formulations contain in total component A) and component B), preferably in a concentration of from 0.01% by weight to 90% by weight, preferably from 0.1% by weight to 75% by weight, more preferably 0 , 25 wt .-% to 50% by weight and most preferably from 0.5% to 40% by weight, the weight percentages being based on the total formulation.
  • these compounds in amounts of less than 1 wt .-%, preferably less than 0.1 wt .-%, more preferably less than 0.01 wt .-% based on the total formulation, in particular no detectable amounts , are included.
  • anionic surfactants present in the formulations according to the invention are known to the person skilled in the art from the relevant prior art for detergents or cleaners. These include, in particular, aliphatic sulfates such as fatty alcohol sulfates, monoglyceride sulfates and ester sulfonates (sulfo fatty acid esters), lignosulfonates, alkylbenzenesulfonates, fatty acid cyanamides, anionic sulfosuccinic acid surfactants, fatty acid isethionates, acylaminoalkanesulfonates (fatty acid taurides), fatty acid sarcosinates, ether carboxylic acids and alkyl (ether) phosphates.
  • aliphatic sulfates such as fatty alcohol sulfates, monoglyceride sulfates and ester sulfonates (sulfo fatty acid esters), lignosulfonates,
  • formulations may contain further ingredients known to the person skilled in the art.
  • Further ingredients in the amounts customary to the person skilled in the art are selected from the group of nonionic surfactants, sugar surfactants, alkylpolyglycosides, cationic surfactants, water-soluble inorganic and / or organic salts, builder substances, polymeric polycarboxylates, water, organic water-miscible solvents, such as. e.g. Ethanol, propanol, iso-propanol, glycols, ethylene glycol, 1,2-propylene glycol, thickener, perfume, dyes.
  • additives for improving the drainage and drying behavior, for adjusting the viscosity, for stabilization and other auxiliaries and additives customary for use in hand dishwashing detergents such as UV stabilizers, perfume, pearlescing agents (INCI Opacifying Agents, for example glycol distearate, eg Cutina ® AGS of the company.
  • Cognis or this containing Mixtures, for example Euperlane® from Cognis), dyes, corrosion inhibitors, preservatives (for example the technical 2-bromo-2-nitropropane-1,3-diol (also referred to as Bronopol) CAS 52-51-7 ), which is commercially available, for example, as Myacide® BT or Boots Bronopol BT from Boots, isothiazolinone derivatives such as chloromethylisothiazolinone (CMIT), methylisothiazolinone (MIT) or benzisothiazolinone (BIT)), organic salts, disinfectants, enzymes, pH adjusters and Skin feel-improving or nourishing additives (eg dermatologically active substances such as vitamin A, vitamin B2, vitamin B12, vitamin C, vitamin E, D-panthenol, sericerin, collagen partial hydrolyzate, various vegetable protein partial hydrolyzates,
  • preservatives for example the technical 2-bromo-2-nitropropane-1,3
  • Another object of the invention is the use of the formulations according to the invention for foam stabilization.
  • Preferably used components A) and B) and combinations thereof are those which have been mentioned above as being preferred in the formulations according to the invention.
  • the weight ratio of component A) to component B) in the use according to the invention 5: 95 to 95: 5, preferably from 15: 85 to 75: 25 and most preferably from 30: 70 to 50:50.
  • Another object of the invention is the use of the formulations according to the invention for the removal of grease and / or oil-containing soiling of hard surfaces, such as but not limited to ceramic dishes.
  • Another object of the invention is the use of the formulations according to the invention for improving the flow behavior of water on hard surfaces, in particular ceramic, glass and / or plastic.
  • Another object of the invention is the use of the formulations according to the invention for improving the drying behavior of hard surfaces, in particular drip-free draining, in particular ceramic, glass and / or plastic.
  • Another use of the formulations of the invention is the prevention of limescale, especially on ceramic, glass and / or plastic.
  • Example 1 foaming behavior and foam volume
  • the sophorolipid "SL 18" used was a soporolipid from Ecover, which has an acid to lactone ratio of 70:30 and a lactone form to oleic acid ratio of 60: 1.
  • the sophorolipid "SL 19" used was a sophorolipd with an acid to lactone ratio of 70:30, which has a lactone form to oleic acid ratio of 6 by addition of oleic acid (Oleic Acid, Cremer Oleo GmbH and Co. KG, Germany).
  • SLES sodium lauryl ether sulfate with 2 EO (Texapon® N 70 trade name of BASF SE,)
  • CAPB cocoamidopropylbetaine, (Tego® betaine C 60 (trade name of Evonik Industries AG))
  • CAPAO cocamidopropylamine oxide (REWOMINOX ⁇ B 204, trade name of Evonik Industries AG)
  • LAO cocoamine oxide.
  • compositions Composition (weight ratio) Foaming [time up to 1000 ml volume] foaming power SLES 100 + ++ CAPB 100 + ⁇ SL 18 100 + ++ SL 19 100 - - CAPAO 100 + + LAO 100 + + CAPB / SL 18 75/25 ++ ++ CAPB / SL 19 75/25 + + CAPAO / SL 18 50/50 ⁇ + CAPAO / SL 19 50/50 - - CAPAO / SL 18 75/25 ⁇ ++ CAPAO / SL 19 75/25 - - LAO / SL 18 75/25 + ++ LAO / SL 19 75/25 - - -
  • sophorolipids having a higher lactone to oleic acid ratio alone and in the selected combinations have excellent foaming properties, both in foaming behavior and in maximum foaming power.
  • the formulations according to the invention have an approximately equally good foaming behavior and an equally good foam stability as the anionic surfactant SLES.
  • the formulations listed here were based on their foaming behavior and the foam stability in accordance with the IKW drop foam method ( Soap Oils Fat Waxes Journal, 128. (2002 ).
  • the method described there was adapted as follows: 20 ml of a 0.02% strength by weight aqueous surfactant solution, the percentage by weight being based on the active substance of the surfactants present in the solution, were introduced into a 2 liter plastic measuring cylinder. From a height of 1 meter 1 liter of water was discharged from 40 ° C and ⁇ 4 ° dH, from a dropping funnel in a shot in the cylinder. It should be noted that the Outflow opening of the dropping funnel is positioned exactly in the middle of the opening of the stationary cylinder. After all the water had been added, the time was stopped and the volume of lather forming was read after 30 seconds and 90 seconds. The 30 second value is characteristic of the foaming behavior and the 90 second value is characteristic for the foam stability.
  • SLES Texapon® N 70 (trade name of BASF SE, sodium lauryl ether sulfate with 2 EO)
  • sophorolipid "SL 18" a soporolipod from Ecover was used, which has an acid to lactone ratio of 70:30 and a lactone form to oleic acid ratio of 60: 1.
  • CAPB Tego® betaine C 60 (trade name of Evonik Industries AG, Cocoamidopropylbetaine)
  • Table 1 The numerical values in Table 1 indicate the weight fraction of each surfactant in relation to the total concentration of 0.02% by weight.
  • the foam values are average values from three measurements each.
  • Table 1 formulation SLES CAPB SL 18 Foam in [ml] after 30 sec Foam in [ml] after 90 sec 1 (comparative example) 70 30 0 773 706 2 70 22.5 7.5 1039 972 3 70 15 15 1132 1079 4 70 7.5 22.5 1079 1026 5 70 0 30 1079 1026 6 80 10 10 1199 1146 7 80 15 5 1252 1173 8 (comparative example) 80 20 0 1093 1012
  • Table 1 Combinations tested for their foaming power without dirt added. Formulations 1 and 8 are not comparative examples according to the invention.
  • Table 2 shows formulations and their foaming power in the presence of olive oil as a soil.
  • the numerical values in Table 2 indicate the weight fraction of the respective surfactant in relation to the total concentration of 0.02% by weight.
  • the foam values are average values from three measurements each Table 2 formulation SLES CAPB SL 18 Foam in [ml] after 30 sec Foam in [ml] after 90 sec 1 (comparative example) 70 30 0 240 227 2 70 22.5 7.5 240 213 3 70 15 15 346 293 4 70 7.5 22.5 253 213 5 70 0 30 213 187
  • the determination of the fat dissolving power was carried out according to the following test scheme.
  • the test soil used was a high-grease and oil-containing soil of the following composition (in% by weight) 2.5% coconut oil (Palmin) 2.5% beef tallow 2.5% olive oil 2.5% rapeseed oil 2.5% corn oil 2.5% milk powder 5% flour. 80% isopropanol
  • the mixture was stained with Sudan Red dye.
  • the soil mixture was freshly prepared before each experiment. As test objects to be cleaned, commercial white ceramic saucers with a diameter of 14 cm were used. The plates were cleaned in a commercial dishwashing machine prior to use and rubbed with ethyl acetate to remove residual fat and allowed to dry overnight. Twenty plates were used for each trial and marked on the bottom for unambiguous identification. The soil mixture was melted and 0.25 g of the liquid soil was applied evenly, circularly in a thin layer in the center of each plate. The plates are then dried at 40 ° C for twelve hours in a drying oven and weighed after cooling to room temperature.
  • the plates are fixed on a 22 ° inclined plane and poured with 20 ml of a temperature-controlled at 40 ° C rinse solution (0.02% active on surfactants).
  • the rinse solution is applied to the plate at a distance of 2 cm using a thin plastic tube at the top edge of the smudge.
  • the mixture was then rinsed with 20 ml of 40 ° C tempered water. Due to the inclined inclination of the dish, the detergent flows off with the detached and dispersed dirt.
  • the plates are then placed upright for two hours on a dish rack. This is followed by drying for 12 h in a drying oven at 40 ° C.
  • the plates are again balanced after cooling to room temperature. The difference of the plate masses with dirt before and after rinsing gives the cleaning power.
  • SLES Texapon® N 70 (trade name of BASF SE, sodium lauryl ether sulfate with 2 EO)
  • SL 18 Soporolipid from Ecover used, which has an acid to lactone ratio of 70:30 and a lactone form to oleic acid ratio of 60: 1.
  • the typical use concentration of formulations F1, F2, F4 and F5 as hand dishwashing detergents are 5 g formulation per 5 liters of water.
  • the typical use levels of formulation F3 as hand dishwashing detergent are 3g formulation to 5 liters of water.

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)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (12)

  1. Formulation, contenant :
    A) au moins un tensioactif biologique choisi dans le groupe constitué par les sophorolipides,
    B) au moins un tensioactif supplémentaire choisi dans le groupe constitué par les bétaïnes, les sulfates d'alcools gras alcoxylés et les alkylaminoxydes,
    C) au moins un acide gras, choisi dans le groupe constitué par les acides β-hydroxy-décanoïques dimères, l'acide oléique, l'acide palmitique, l'acide stéarique et l'acide linoléique,
    caractérisée en ce que le rapport en poids entre le sophorolipide sous la forme lactone et le composant C) est compris entre 50:1 et 80:1.
  2. Formulation selon la revendication 1, caractérisée en ce que le composant B) est choisi dans le groupe constitué par les alkylbétaïnes, les alkylamidobétaïnes, les imidazolinium-bétaïnes, les sulfobétaïnes et les phosphobétaïnes.
  3. Formulation selon la revendication 1 ou 2, caractérisée en ce que le composant B) est choisi dans le groupe constitué par la cocamidopropylbétaïne, les lauryléthersulfates éthoxylés avec 1 à 4 EO, le cocamidopropylaminoxyde et le cocoaminoxyde.
  4. Formulation selon au moins l'une quelconque des revendications précédentes, caractérisée en ce que
    le composant A) est un sophorolipide et
    le composant B) comprend de la cocamidopropylbétaïne et du lauryléthersulfate éthoxylé avec 1 à 4 EO.
  5. Formulation selon au moins l'une quelconque des revendications précédentes, caractérisée en ce que le composant A) est contenu en une concentration de 0,01 % en poids à 95 % en poids, de préférence de 0,1 % en poids à 40 % en poids, de manière particulièrement préférée de 1 % en poids à 20 % en poids, les pourcentages en poids se rapportant à la formulation totale.
  6. Formulation selon au moins l'une quelconque des revendications précédentes, caractérisée en ce que le composant B) est contenu en une concentration de 0,01 % en poids à 95 % en poids, de préférence de 0,1 % en poids à 50 % en poids, de manière particulièrement préférée de 1 % en poids à 30 % en poids, les pourcentages en poids se rapportant à la formulation totale.
  7. Formulation selon au moins l'une quelconque des revendications précédentes, caractérisée en ce que le rapport en poids entre le composant A) et le composant B) dans la formulation selon l'invention est de 5:95 à 95:5, de préférence de 15:85 à 75:25 et de manière tout particulièrement préférée de 30:70 à 50:50.
  8. Formulation selon au moins l'une quelconque des revendications précédentes, caractérisée en ce que le composant A) et le composant B) au total en une concentration de 0,01 % en poids à 90 % en poids, de préférence de 0,1 % en poids à 75 % en poids, de manière particulièrement préférée de 0,25 % en poids à 50 % en poids et de manière tout particulièrement préférée de 0,5 % en poids à 40 % en poids, les pourcentages en poids se rapportant à la formulation totale.
  9. Utilisation d'une formulation selon au moins l'une quelconque des revendications précédentes pour la stabilisation d'une mousse.
  10. Utilisation d'une formulation selon au moins l'une quelconque des revendications 1 à 8 pour l'élimination de salissures grasses et/ou huileuses sur des surfaces dures.
  11. Utilisation d'une formulation selon au moins l'une quelconque des revendications 1 à 8 pour l'amélioration du comportement d'écoulement de l'eau sur des surfaces dures.
  12. Utilisation d'une formulation selon au moins l'une quelconque des revendications 1 à 8 pour l'amélioration du comportement de séchage de surfaces dures.
EP15760136.0A 2014-09-30 2015-09-02 Formule contenant des bio-tenseurs Active EP3201302B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14186999.0A EP3002328A1 (fr) 2014-09-30 2014-09-30 Formule contenant des bio-tenseurs
PCT/EP2015/070023 WO2016050439A1 (fr) 2014-09-30 2015-09-02 Formulation contenant des tensioactifs biologiques

Publications (2)

Publication Number Publication Date
EP3201302A1 EP3201302A1 (fr) 2017-08-09
EP3201302B1 true EP3201302B1 (fr) 2019-05-15

Family

ID=51726325

Family Applications (2)

Application Number Title Priority Date Filing Date
EP14186999.0A Withdrawn EP3002328A1 (fr) 2014-09-30 2014-09-30 Formule contenant des bio-tenseurs
EP15760136.0A Active EP3201302B1 (fr) 2014-09-30 2015-09-02 Formule contenant des bio-tenseurs

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP14186999.0A Withdrawn EP3002328A1 (fr) 2014-09-30 2014-09-30 Formule contenant des bio-tenseurs

Country Status (6)

Country Link
US (1) US20170306264A1 (fr)
EP (2) EP3002328A1 (fr)
JP (1) JP6661623B2 (fr)
CN (1) CN107001987A (fr)
BR (1) BR112017006137B1 (fr)
WO (1) WO2016050439A1 (fr)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3419986B1 (fr) 2016-02-22 2025-11-05 Evonik Operations GmbH Rhamnolipidamides pour la retention des parfums pour les cheveux
US10676495B2 (en) 2016-02-22 2020-06-09 Evonik Operations Gmbh Rhamnolipid esters as nonionic surfactants for cosmetic use
JP2019508564A (ja) * 2016-03-18 2019-03-28 エボニック デグサ ゲーエムベーハーＥｖｏｎｉｋ Ｄｅｇｕｓｓａ ＧｍｂＨ 少なくとも１種のバイオサーファクタントがその上に含まれる無機固体担体を含む顆粒
PL3478655T3 (pl) 2016-06-29 2021-03-22 Evonik Operations Gmbh Sposób wytwarzania tenzydów
EP3487945B1 (fr) 2016-07-19 2020-05-13 Evonik Operations GmbH Utilisation d'esters de polyols destines a la production de revetements plastiques poreux
CH712858A2 (de) 2016-08-29 2018-03-15 Remo Richli Milde Zubereitungen mit alkoxylierten Fettsäureamiden und Glycolipid-Biotensiden.
CH712860A2 (de) 2016-08-29 2018-03-15 Remo Richli Mittel mit alkoxylierten Fettsäureamiden und Glycolipid-Biotensiden.
CH712859A2 (de) 2016-08-29 2018-03-15 Remo Richli Wasch-, Pflege- und Reinigungsmittel mit Polyoxyalkylen Carboxylat und Glycolipid-Biotensid.
CN110167347B (zh) 2016-10-07 2022-07-15 赢创运营有限公司 包含糖脂和防腐剂的组合物
CN110267641A (zh) 2017-02-10 2019-09-20 赢创德固赛有限公司 含有至少一种生物表面活性剂和氟化物的口腔护理组合物
US11576849B2 (en) * 2017-03-30 2023-02-14 Conopco, Inc. Antimicrobial personal cleansing compositions
WO2018197623A1 (fr) 2017-04-27 2018-11-01 Evonik Degussa Gmbh Composition nettoyante biodégradable
CN110719951A (zh) * 2017-04-27 2020-01-21 赢创德固赛有限公司 生物可降解的清洁组合物
US11696885B2 (en) 2017-08-24 2023-07-11 Evonik Operations Gmbh Rhamnolipid derivatives as emulsifiers and dispersing aids
JP7428637B2 (ja) 2017-08-30 2024-02-06 エボニック オペレーションズ ゲーエムベーハー 多孔質プラスチック被覆を製造するためのポリオールエーテルの使用
CN114836266B (zh) 2017-11-07 2024-06-11 埃科莱布美国股份有限公司 用于去除唇用化妆品污渍的清洁组合物和方法
EP3688129B1 (fr) 2017-12-07 2025-08-06 Ecolab USA, Inc. Compositions et procédés d'élimination de rouge à lèvres à l'aide de polyamines ramifiées
WO2019154970A1 (fr) 2018-02-09 2019-08-15 Evonik Degussa Gmbh Composition de mélange comprenant des glucolipides
EP3546589B1 (fr) 2018-03-29 2022-08-10 Evonik Operations GmbH Procédé de production de sphingolipides
US20220023176A1 (en) * 2018-11-26 2022-01-27 Shiseido Company, Ltd. Cleansing composition
EP3686265A1 (fr) 2019-01-23 2020-07-29 BlueSun Consumer Brands, S.L. Composition détergente avec sophorolipides
WO2020179819A1 (fr) * 2019-03-05 2020-09-10 日産化学株式会社 Composition d'agent de nettoyage, et procédé de nettoyage
DE102019207064A1 (de) 2019-05-15 2020-11-19 Henkel Ag & Co. Kgaa biotensidhaltige Zahncremes
US11918670B2 (en) 2020-03-11 2024-03-05 Evonik Operations Gmbh Mixture composition comprising glycolipids and triethyl citrate
WO2022017844A1 (fr) 2020-07-22 2022-01-27 Evonik Operations Gmbh Nouveaux oligoesters de rhamnolipides
EP4263771B1 (fr) * 2020-12-17 2025-02-12 Unilever IP Holdings B.V. Utilisation d'une composition de nettoyage pour améliorer les performances de nettoyage à froid
WO2022214954A1 (fr) 2021-04-06 2022-10-13 LignoSol IP Limited Fluides de forage à base de lignine et procédés associés
US12600896B2 (en) 2021-04-06 2026-04-14 LignoSol IP Limited Lignin-based compositions and related hydrocarbon recovery methods
JP2024514838A (ja) * 2021-04-06 2024-04-03 リグノソル・アイピー・リミテッド リグニンベースの組成物及び関連方法
MX2023011899A (es) 2021-04-06 2024-05-06 Lignosol Ip Ltd Diluyente a base de lignina y metodos relacionados.
US20240301324A1 (en) * 2021-08-09 2024-09-12 Croda International Plc Composition
CN113881441B (zh) * 2021-11-11 2022-05-10 中节能（连云港）清洁技术发展有限公司 落地油泥资源化和无害化处理工艺、油泥生物炭及其应用
WO2024002738A1 (fr) 2022-06-28 2024-01-04 Evonik Operations Gmbh Composition contenant un biotensioactif et de la persicomycine
DE102022210849A1 (de) * 2022-10-14 2024-04-25 Henkel Ag & Co. Kgaa Sophorolipid-Tenside mit oberflächenaktiven Gegenkationen
CH720165A2 (de) 2022-10-26 2024-04-30 Chemtek Ug Zusammensetzungen mit N-Acylglycaminen
EP4637737A1 (fr) 2022-12-21 2025-10-29 Evonik Operations GmbH Compositions contenant des biotensioactifs et des desferrioxamines
WO2025036643A1 (fr) 2023-08-15 2025-02-20 Evonik Operations Gmbh Biotensioactif pour le lavage de laine
GB202409571D0 (en) * 2024-07-02 2024-08-14 Innospec Performance Chemicals Italia Srl Detergent composition

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9102945D0 (en) 1991-02-12 1991-03-27 Unilever Plc Detergent composition
DE19600743A1 (de) 1996-01-11 1997-07-24 Henkel Kgaa Verwendung von Mischungen aus Glycolipiden und Tensiden
JP2003013093A (ja) 2001-06-27 2003-01-15 Saraya Kk 低泡性洗浄剤組成物
JP2003128512A (ja) * 2001-10-18 2003-05-08 Showa Denko Kk 化粧料用抗菌性組成物
DE60305861T2 (de) 2003-01-28 2007-01-04 Ecover N.V. Reinigungsmittelzusammensetzungen
JP2008069075A (ja) * 2006-09-12 2008-03-27 Kracie Home Products Kk 皮膚外用組成物
JP5649268B2 (ja) * 2008-05-15 2015-01-07 サラヤ株式会社 ソホロリピッドを含む吸着抑制組成物
JP2011026276A (ja) * 2009-07-29 2011-02-10 Toyobo Co Ltd バイオサーファクタントを用いた毛髪化粧料
DE102009046169A1 (de) * 2009-10-29 2011-05-05 Henkel Ag & Co. Kgaa Rückstandsarmer Reiniger für harte Oberflächen
DE102010014680A1 (de) 2009-11-18 2011-08-18 Evonik Degussa GmbH, 45128 Zellen, Nukleinsäuren, Enzyme und deren Verwendung sowie Verfahren zur Herstellung von Sophorolipiden
BR112012025016B1 (pt) 2010-03-31 2018-02-14 Unilever N.V. Composição espumante e de suavização da pele para higiene pessoal, sabonete líquido ou xampu, e, seu uso
CN103946359A (zh) * 2011-09-15 2014-07-23 荷兰联合利华有限公司 包含表面活性剂和酶的洗涤剂组合物
JP2014526604A (ja) * 2011-09-20 2014-10-06 ザ プロクター アンド ギャンブル カンパニー イソプレノイド由来界面活性剤を含む持続可能な界面活性剤系を含む洗剤組成物
DE102011090030B4 (de) 2011-12-28 2025-11-06 Evonik Operations Gmbh Wässrige Haar- und Hautreinigungszusammensetzungen, enthaltend Biotenside
CN102660394A (zh) * 2012-05-09 2012-09-12 中航材航空新材料有限公司 水基型纯天然环保清洗剂及其制备方法
CN104869978B8 (zh) * 2012-12-17 2017-09-12 荷兰联合利华有限公司 个人护理组合物
DE102013205755A1 (de) * 2013-04-02 2014-10-02 Evonik Industries Ag Waschmittelformulierung für Textilien enthaltend Rhamnolipide mit einem überwiegenden Gehalt an di-Rhamnolipiden
DE102013206314A1 (de) * 2013-04-10 2014-10-16 Evonik Industries Ag Kosmetische Formulierung enthaltend Copolymer sowie Sulfosuccinat und/oder Biotensid
CN103773623B (zh) * 2014-02-25 2017-05-17 衢州华宇科技有限公司 一种复合酶洗涤剂及其制备方法和用途

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
US20170306264A1 (en) 2017-10-26
BR112017006137B1 (pt) 2022-10-11
BR112017006137A2 (pt) 2018-02-06
JP2017530241A (ja) 2017-10-12
EP3002328A1 (fr) 2016-04-06
CN107001987A (zh) 2017-08-01
JP6661623B2 (ja) 2020-03-11
EP3201302A1 (fr) 2017-08-09
WO2016050439A1 (fr) 2016-04-07

Similar Documents

Publication Publication Date Title
EP3201302B1 (fr) Formule contenant des bio-tenseurs
EP1317522B1 (fr) Agent de lavage et de nettoyage a sechage rapide, notamment liquide de vaisselle a la main
EP2401351B1 (fr) Liquide vaisselle
EP1564283B1 (fr) combinaison de tensio-actifs
EP3290501B1 (fr) Compositions detergentes contentant des amides d'acides gras alcoxylés
EP1352628B1 (fr) Concentré aqueux de lustre nacré
DE102009002262A1 (de) Präbiotische Handgeschirrspülmittel
WO2014009027A1 (fr) Epaississant stable aux lipases
EP0942706B1 (fr) Concentres aqueux de lustre perlaire
EP3744819A1 (fr) Composition comprenant des acides gras alcoxylés
EP3536769A1 (fr) Composition d'agent de lavage et de nettoyage
EP1306423B1 (fr) Méthode pour accélérer le pouvoir séchant des compositions nettoyantes aqueuses comprenant des agents tensioactifs
WO2007118748A1 (fr) Détergent aqueux
EP1133545B1 (fr) Nettoyant tous usages contenant un polysiloxane diquaternaire
DE69518393T2 (de) Reinigungsmittelzusammensetzung
EP0912700B1 (fr) Concentres aqueux de lustre nacre
DE10162648A1 (de) Sprühbares, schnelltrocknendes Reinigungsmittel
EP0999822B1 (fr) Concentres aqueux nacres
DE19527596A1 (de) Wäßrige Tensidmischung
DE102020132485A1 (de) Ökologisch nachhaltige Handgeschirrspülmittelzusammensetzung mit Zuckertensiden
DE102012221021A1 (de) Wasch- und Reinigungsmittel mit Alkylpolypentosiden
EP0670878A1 (fr) Preparations tensio-actives visqueuses aqueuses
EP3502223A1 (fr) Détergent pour vaisselle à la main contenant oxyde d'amine
DE102010043896A1 (de) Verwendung von in situ hergestellter Zinkseife
DE102008003555A1 (de) Handgeschirrspülmittel mit APG

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

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

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

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20170306

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

DAV Request for validation of the european patent (deleted)
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: 20180327

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: 20190218

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: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502015009087

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20190515

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

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

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: 20190515

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: 20190515

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: 20190515

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: 20190515

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: 20190915

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: 20190815

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: 20190515

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: 20190515

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: 20190515

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

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: 20190815

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: 20190816

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: 20190515

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: 20190515

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

Owner name: EVONIK OPERATIONS GMBH

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 502015009087

Country of ref document: DE

Owner name: EVONIK OPERATIONS GMBH, DE

Free format text: FORMER OWNER: EVONIK DEGUSSA GMBH, 45128 ESSEN, DE

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

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: 20190515

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: 20190515

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: 20190515

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: 20190515

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 502015009087

Country of ref document: DE

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: 20190515

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: 20190515

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

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: 20190515

26N No opposition filed

Effective date: 20200218

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

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: 20190515

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

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: 20190515

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: 20190515

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: CH

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

Effective date: 20190930

Ref country code: LI

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

Effective date: 20190930

Ref country code: IE

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

Effective date: 20190902

Ref country code: LU

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

Effective date: 20190902

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190930

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: 20190930

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

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: 20190515

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: 20190515

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: 20190915

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: 20190515

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: 20150902

REG Reference to a national code

Ref country code: AT

Ref legal event code: MM01

Ref document number: 1133434

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200902

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

Ref country code: AT

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

Effective date: 20200902

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: 20190515

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

Free format text: CASE NUMBER: UPC_APP_328158/2023

Effective date: 20230524

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

Ref country code: DE

Payment date: 20250919

Year of fee payment: 11

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

Ref country code: GB

Payment date: 20250919

Year of fee payment: 11

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

Ref country code: FR

Payment date: 20250922

Year of fee payment: 11