WO2017174252A1 - Composition de détergent à lessive - Google Patents

Composition de détergent à lessive Download PDF

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Publication number
WO2017174252A1
WO2017174252A1 PCT/EP2017/053800 EP2017053800W WO2017174252A1 WO 2017174252 A1 WO2017174252 A1 WO 2017174252A1 EP 2017053800 W EP2017053800 W EP 2017053800W WO 2017174252 A1 WO2017174252 A1 WO 2017174252A1
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WO
WIPO (PCT)
Prior art keywords
laundry detergent
detergent composition
aqueous liquid
liquid laundry
composition according
Prior art date
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PCT/EP2017/053800
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English (en)
Inventor
Stephen Norman Batchelor
Jayne Michelle Bird
Matthew Lloyd Parry
Original Assignee
Unilever Plc
Unilever N.V.
Conopco, Inc., D/B/A Unilever
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 Unilever Plc, Unilever N.V., Conopco, Inc., D/B/A Unilever filed Critical Unilever Plc
Priority to EP17708995.0A priority Critical patent/EP3440170B1/fr
Priority to CN201780020519.8A priority patent/CN109072131A/zh
Priority to BR112018070472-5A priority patent/BR112018070472B1/pt
Publication of WO2017174252A1 publication Critical patent/WO2017174252A1/fr

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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
    • C11D1/02—Anionic compounds
    • C11D1/37—Mixtures of compounds all of which are anionic
    • 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3715—Polyesters or polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723—Polyamines or polyalkyleneimines
    • 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
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—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
    • C11D1/72—Ethers of polyoxyalkylene glycols

Definitions

  • the present invention provides an alkoxylated polyethylene imine polymer and surfactant formulation for use in domestic laundry.
  • WO2014/060235 discloses a laundry detergent composition comprising (a) nonionic surfactant, (b) anionic surfactant, (c) alkyl ether carboxylic acid or carboxylate salt thereof, and, (d) a polyglucosamine or a copolymer of glucosamine and N- acetylglucosamine; and to its use to soften fabrics.
  • the present invention provides an aqueous liquid laundry detergent composition
  • aqueous liquid laundry detergent composition comprising: (i) from 2 to 15 wt%, preferably from 3 to 8 wt%, of linear alkyl benzene sulfonate anionic surfactant;
  • R2 is selected from saturated and mono-unsaturated C10 to C26 linear or branched alkyl chains, preferably a C12 to C20 linear alkyl chains, most preferably a C16 to C18 linear alkyl chain, and wherein n is selected from: 2 to 20, preferably 7 to 13, more preferably 8 to 12, most preferably 9.5 to 10.5;
  • laundry detergent composition comprises in total from 10 to 20 wt% of anionic surfactant.
  • the present invention provides a domestic method of treating a textile, the method comprising the steps of:
  • the surfactant used is preferably as preferred for the composition aspects of the present invention.
  • Domestic methods are preferably conducted in a domestic washing machine or by hand washing.
  • the temperature of the wash is preferably from 285 to 313K.
  • the main wash time is preferably 5 to 45 minutes.
  • the textile is preferably an item of clothing, bedding or table cloth.
  • Preferred items of clothing are cotton containing shirts, skirts, dresses trousers, underwear and jumpers.
  • Linear alkyl benzene sulfonate Weights of Linear alkyl benzene sulfonate are calculated as the protonated form.
  • the linear alkyl benzene sulfonate has an alkyl chain length of C8 to C15, preferably C12 to C14.
  • Linear alkyl benzene sulphonate may be obtained, by sulphonating commercially available linear alkyl benzene (LAB); suitable LAB includes low 2-phenyl LAB, such as those supplied by Sasol under the tradename Isochem® or those supplied by Petresa under the tradename Petrelab®, other suitable LAB include high 2-phenyl LAB, such as those supplied by Sasol under the tradename Hyblene®.
  • Another suitable route is alkyl benzene sulphonate that is obtained by DETAL catalyzed process, preferably having 8 to 15 carbon atoms. Other synthesis routes, such as HF, may also be suitable.
  • Weights of alkyl ether sulfate are calculated as the protonated form, Ri-(OCH2CH2) m - OSO3H.
  • Ri is C10 to C22 saturate or unsaturated linear alkyl chain, more preferably a saturated C12 to C16 linear alkyl chain, most preferably C12 linear alkyl chain (lauryl).
  • the ratio (wt% alkyl ether sulfate)/(wt% linear alkyl benzene sulfonate) is from 0.5 to 2, more preferably 0.7 to 1 .2.
  • Weights of alkyl ether carboxylic acid are calculated as the protonated form, R2-(OCH2CH2) n - OCH2COOH . They may be used as salt version for example sodium salt, or amine salt.
  • the alkyl chain, R2 may be linear or branched, preferably it is linear.
  • the alkyl chain, R2, may be aliphatic or contain one cis or trans double bond.
  • the alkyl ether carboxylic acid is most preferably of the structure:
  • Alkyl ether carboxylic acid are available from Kao (Akypo ®), Huntsman (Empicol®) and Clariant (Emulsogen ®).
  • the sodium salt of the alkyl ether carboxylate may be used.
  • Zwitterionic surfactants are preferably absent from the formulation.
  • Zwitterionic surfactants contain a charges group with a formal positive and a formal negative charge.
  • the aqueous liquid laundry detergent composition comprises less than 0.1 wt% of a zwitterionic surfactant; most preferably 0 wt% of a zwitterionic surfactant.
  • Typical examples of zwitterionic surfactants are carbobetaines and amine oxides.
  • the aqueous liquid laundry detergent may comprise Non-ionic surfactant, preferably an alkyl ethoxylated non-ionic surfactant.
  • Suitable nonionic detergent compounds which may be used include, in particular, the reaction products of compounds having an aliphatic hydrophobic group and a reactive hydrogen atom, for example, polyaryllphenols, aliphatic alcohols, acids or amides, especially ethylene oxide either alone or with propylene oxide.
  • the preferred nonionic detergent compounds are the condensation products of aliphatic Cs to Cis primary or secondary linear or branched alcohols with ethylene oxide.
  • the alkyl ethoxylated non-ionic surfactant is a C12 to C15 primary alcohol with a mole average ethoxylation of 7EO to 9EO units.
  • the weight fraction of alkyl ether sulphate/non-ionic surfactant is preferably greater than 3.
  • the aqueous liquid laundry detergent may comprises from 0 to 4 wt% of further surfactants, for example, those described in Anionic Surfactants: Organic Chemistry edited by
  • Suitable further anionic detergent compounds are; alkyl sulphates, especially those obtained by sulphating linear or branched Cs to Cis alcohols; soaps; alkyl (preferably methyl) ester sulphonates, and mixtures thereof. Soaps are particularly preferred in the aqueous liquid laundry detergent composition at levels of 0.5 to 1 .5 wt%. Weights refer to protonated forms.
  • the alkoxylated polyethyelene imine comprises a polyethyleneimine (PEI) backbone wherein the modification of the polyethyleneimine backbone is intended to leave the polymer without quaternisation.
  • PEI polyethyleneimine
  • Such materials may be represented as PEI(X)YAO where X represents the molecular weight of the unmodified PEI and Y represents the average moles of alkoxylation (AO) per available NH in the unsubstituted polyethyleneimine backbone.
  • Y is preferably from 7 to 40 more preferably it is in the range from 16 to 26, most preferably 18 to 22.
  • X is selected to be from about 300 to about 10000 weight average molecular weight and is preferably from 500 to 800.
  • the alkoxylation is preferably selected from ethoxylation or propoxylation, or a combination of the two, Ethoxylation is most preferred.
  • the alkoxy chains may be capped with groups selected from: H; CH3; SO3 " ; CH2COO " ; PO3 2" ; C2H5; n-propyl, i-propyl; n-butyl; t-butyl; and, sulfosuccinate, most preferably H.
  • alkoxylated PEI is PEI(600)20EO.
  • PEI(600)10EO7PO PEI(1600)19EO
  • PEI80024EO16PO PEI(600)10EO7PO
  • PEI(1600)19EO PEI(1600)19EO
  • PEI80024EO16PO PEI(600)10EO7PO
  • PEI(1600)19EO PEI(1600)19EO
  • PEI80024EO16PO PEI(600)10EO7PO
  • PEI(1600)19EO PEI(1600)19EO
  • PEI80024EO16PO PEI80024EO16PO
  • polymerisation of an alkene bearing a substituent sulfonate group with an alkene bearing a polyoxyalkylene chain and an alkene bearing a carboxy substituents in a weight ratio of from 5:1 to 1 :5 with the alkoxylated polyethyelene imine may be added.
  • the copolymer is obtainable by polymerisation of 5-15wt% 3-allyloxy-2-hydroxypropane sulfonate with 30 to 45 wt% of 3-methylbut-3-en-1-ol which has been reacted with 20 to 40 moles of ethylene oxide; and 25 to 55% acrylic acid or salts thereof.
  • Such polymers are described in WO2016/045518 (Nippon Shokubai).
  • Terephthalate Polyester Soil Release Polymer comprise polymers of aromatic dicarboxylic acids and alkylene glycols (including polymers containing polyalkylene glycols), as described in WO2009/153184, EP2692842 and WO2014/019903.
  • Terephthalate Polyester Soil Release Polymer examples include the REPEL-O-TEX® line of polymers supplied by Rhodia, including REPEL-O-TEX® SRP6 and REPEL-O-TEX® SF-2.
  • Other suitable soil release polymers include TexCare® polymers, including TexCare® SRA- 100, TexCare® SRA-300, TexCare® SRN-100, TexCare® SRN-170, TexCare® SRN-240, TexCare® SRN-300, and TexCare® SRN-325, all supplied by Clariant.
  • Preferred structure are -[(Z) a -0-OC-Ar-CO-] b and (Z) a -0-OC-[Ar-CO-0-C 3 H 6 -0-OC]b-Ar-CO- 0-(Z) a , where Ar is selected from 1 ,4 substituted phenylene and 1 ,3 substituted phenylene substituted in the 5 position with a sulphonates (SO3 " ) group; Z is selected from
  • ethoxy;propoxy; and mixtures of ethoxy and propoxy; a is from 5 to 100 and b from 2 to 40.
  • C3H6 is i-propyl.
  • the alkoxy chains are capped with groups selected from H; CH3; SO3 " ; CH2COO " ; PO3 2" ; C2H5; n-propyl, i-propyl; n-butyl; t-butyl; and, sulfosuccinate.
  • the Terephthalate Polyester Soil Release Polymer is:
  • c is from 4 to 9; d is from 1 to 3; e is from 40 to 50.
  • composition may comprise one or more further polymers. Examples are:
  • carboxymethylcellulose poly (ethylene glycol), polyvinyl alcohol), polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
  • Polymers present to prevent dye deposition may be present, for example
  • Such polymers are preferably present at levels of less than 2 wt%.
  • a particularly preferred additional polymer is that obtained by the amination of the reaction product of a 2,2-bis-alkyl substituted 1 ,3 propanediol with 2 to 10 moles of an alkenyloxide, preferably selected from ethylene oxide, propylene oxide and mixtures thereof.
  • the amination of the alkoxylate 1 ,3-diol may be carried out with ammonia or reductive cyanoethylation.
  • Preferred 1 ,3-diol's are 2-butyl-2-ethyl-1 ,3-propanediol, 2,2-dimethyl-1 ,3- propanediol.
  • Such polyetheramines are described in WO2016/048674 (BASF).
  • composition is preferably devoid of silicone polymers and polymers bearing quaternised N groups.
  • the detergent compositions may also optionally contain relatively low levels of organic detergent builder or sequestrant material.
  • organic detergent builder or sequestrant material examples include the alkali metal, citrates, succinates, malonates, carboxymethyl succinates, carboxylates, polycarboxylates and polyacetyl carboxylates.
  • Specific examples include sodium, potassium and lithium salts of oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, ethylene diamine tetra-acetic acid, diethylenetriamine-pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid, and citric acid.
  • DEQUESTTM organic phosphonate type sequestering agents sold by Monsanto and alkanehydroxy phosphonates.
  • suitable organic builders include the higher molecular weight polymers and copolymers known to have builder properties.
  • such materials include appropriate polyacrylic acid, polymaleic acid, and polyacrylic/polymaleic acid copolymers and their salts, such as those sold by BASF under the name SOKALANTM.
  • the aqueous liquid laundry detergent formunation comprise from 0.1 % to 2.0 wt% builder and sequesterant material. Citrate is most preferred.
  • Shading Dyes for use in laundry detergents preferably have an extinction coefficient at the maximum absorption in the visible range (400 to 700nm) of greater than 5000 L mol "1 cm -1 , preferably greater than 10000 L mol "1 cm -1 .
  • the dyes are blue or violet in colour.
  • Preferred shading dye chromophores are azo, azine, anthraquinone, and triphenylmethane.
  • Preferred mono-azo dyes contain a heterocyclic ring and are most preferably thiophene dyes.
  • Alkoxylated thiophene dyes are discussed in WO/2013/142495 and WO/2008/087497
  • Azine dye are preferably selected from sulphonated phenazine dyes and cationic phenazine dyes.
  • Preferred examples are acid blue 98, acid violet 50, dye with CAS-No 72749-80-5, acid blue 59.
  • the shading dye is present in the composition in range from 0.0001 to 0.5 wt %, preferably 0.001 to 0.1 wt%. Depending upon the nature of the shading dye there are preferred ranges depending upon the efficacy of the shading dye which is dependent on class and particular efficacy within any particular class. As stated above the shading dye is a blue or violet shading dye. A mixture of shading dyes may be used.
  • the shading dye is most preferably a reactive blue anthraquinone dye, such as C.I. reactive blue 49, covalently linked to an alkoxylated polyethyleneimine.
  • the alkoxylation is preferably selected from ethoxylation and propoxylation, most preferably propoxylation.
  • 80 to 95 mol% of the N-H groups in the polyethylene imine are replaced with iso-propyl alcohol groups by propoxylation.
  • the polyethylene imine before reaction with the dye and the propoxylation has a molecular weight of 600 to 1800.
  • the inventive aqueous liquid laundry detergent composition reduces the staining on neat contact of the composition with fabric.
  • proteases hydrolyse bonds within peptides and proteins, in the laundry context this leads to enhanced removal of protein or peptide containing stains.
  • suitable proteases families include aspartic proteases; cysteine proteases; glutamic proteases;
  • proteases aspargine peptide lyase; serine proteases and threonine proteases.
  • protease families are described in the MEROPS peptidase database (http://merops.sanger.ac.uk/). Serine proteases are preferred. Subtilase type serine proteases are more preferred.
  • the term "subtilases" refers to a sub-group of serine protease according to Siezen et al., Protein Engng. 4 (1991 ) 719-737 and Siezen et al. Protein Science 6 (1997) 501 -523.
  • Serine proteases are a subgroup of proteases characterized by having a serine in the active site, which forms a covalent adduct with the substrate.
  • the subtilases may be divided into 6 subdivisions, i.e. the Subtilisin family, the Thermitase family, the Proteinase K family, the Lantibiotic peptidase family, the Kexin family and the Pyrolysin family.
  • subtilases are those derived from Bacillus such as Bacillus lentus, B.
  • subtilase variants may comprise the mutations: S3T, V4I, S9R, A15T, K27R, * 36D,
  • protease is a subtilisins (EC 3.4.21.62).
  • subtilases are those derived from Bacillus such as Bacillus lentus, B.
  • subtilis alkalophilus, B. subtilis, B. amyloliquefaciens, Bacillus pumilus and Bacillus gibsonii described in; US7262042 and WO09/021867, and subtilisin lentus, subtilisin Novo, subtilisin Carlsberg, Bacillus licheniformis, subtilisin BPN', subtilisin 309, subtilisin 147 and subtilisin 168 described in WO89/06279 and protease PD138 described in (WO93/18140).
  • the subsilisin is derived from Bacillus, preferably Bacillus lentus, B. alkalophilus, B. subtilis, B.
  • subtilisin is derived from Bacillus gibsonii or Bacillus Lentus.
  • Suitable commercially available protease enzymes include those sold under the trade names names Alcalase®, Blaze®; DuralaseTm, DurazymTm, Relase®, Relase® Ultra, Savinase®, Savinase® Ultra, Primase®, Polarzyme®, Kannase®, Liquanase®, Liquanase® Ultra, Ovozyme®, Coronase®, Coronase® Ultra, Neutrase®, Everlase® and Esperase® all could be sold as Ultra® or Evity® (Novozymes A/S). Those sold under the tradename Maxatase®, Maxacal®, Maxapem®, Properase®,
  • BLAP Henkel/ Kemira
  • BLAP R BLAP with S3T + V4I + V199M + V205I + L217D
  • BLAP X BLAP with S3T + V4I + V205I
  • BLAP F49 BLAP with S3T + V4I + A194P + V199M + V205I + L217D
  • One or more further enzymes are preferred present in a laundry composition of the invention and when practicing a method of the invention.
  • the level of each enzyme in the laundry composition of the invention is from 0.0001 wt% to 0.1 wt% protein.
  • the further enzyme is selected from: alpha-amylases; lipases; and, cellulases, most preferably an alpha-amylase (EC number 3.2.1.1. ).
  • Suitable lipases include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Examples of useful lipases include lipases from Humicola (synonym Thermomyces), e.g. from H. lanuginosa (T. lanuginosus) as described in EP 258 068 and EP 305 216 or from H. insolens as described in WO 96/13580, a Pseudomonas lipase, e.g. from P. alcaligenes or P. pseudoalcaligenes (EP 218 272), P. cepacia (EP 331 376), P. stutzeri (GB 1 ,372,034), P.
  • lipase variants such as those described in WO 92/05249,
  • LipolaseTM and Lipolase UltraTM LipexTM and LipocleanTM (Novozymes A/S).
  • the method of the invention may be carried out in the presence of phospholipase classified as EC 3.1.1 .4 and/or EC 3.1.1.32.
  • phospholipase is an enzyme which has activity towards phospholipids.
  • Phospholipids such as lecithin or phosphatidylcholine, consist of glycerol esterified with two fatty acids in an outer (sn-1 ) and the middle (sn-2) positions and esterified with phosphoric acid in the third position; the phosphoric acid, in turn, may be esterified to an amino-alcohol.
  • Phospholipases are enzymes which participate in the hydrolysis of phospholipids.
  • phospholipases Ai and A2 which hydrolyze one fatty acyl group (in the sn-1 and sn-2 position, respectively) to form lysophospholipid
  • lysophospholipase or phospholipase B
  • Phospholipase C and phospholipase D release diacyl glycerol or phosphatidic acid respectively.
  • the method of the invention may be carried out in the presence of cutinase classified in EC 3.1 .1 .74.
  • the cutinase used according to the invention may be of any origin.
  • Preferably cutinases are of microbial origin, in particular of bacterial, of fungal or of yeast origin.
  • Suitable amylases include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included.
  • Amylases include, for example, alpha- amylases obtained from Bacillus, e.g. a special strain of B. lichen iformis, described in more detail in GB 1 ,296,839, or the Bacillus sp.
  • Suitable cellulases include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Suitable cellulases include cellulases from the genera Bacillus, Pseudomonas, Humicola, Fusarium, Thielavia, Acremonium, e.g. the fungal cellulases produced from Humicola insolens, Thielavia terrestris, Myceliophthora
  • thermophila and Fusarium oxysporum disclosed in US 4,435,307, US 5,648,263, US 5,691 ,178, US 5,776,757, WO 89/09259, WO 96/029397, and WO 98/012307.
  • Commercially available cellulases include CelluzymeTM, CarezymeTM, CellucleanTM, EndolaseTM, RenozymeTM (Novozymes A/S), ClazinaseTM and Puradax HATM (Genencor International Inc.), and KAC-500(B)TM (Kao Corporation). CellucleanTM is preferred.
  • Suitable peroxidases/oxidases include those of plant, bacterial or fungal origin. Chemically modified or protein engineered mutants are included.
  • peroxidases examples include peroxidases from Coprinus, e.g. from C. cinereus, and variants thereof as those described in WO 93/24618, WO 95/10602, and WO 98/15257.
  • Commercially available peroxidases include GuardzymeTM and NovozymTM 51004 (Novozymes A/S).
  • Any enzyme present in the composition may be stabilized using conventional stabilizing agents, e.g., a polyol such as propylene glycol or glycerol, a sugar or sugar alcohol, lactic acid, boric acid, or a boric acid derivative, e.g., an aromatic borate ester, or a phenyl boronic acid derivative such as 4-formylphenyl boronic acid, and the composition may be formulated as described in e.g., WO 92/19709 and WO 92/19708.
  • a polyol such as propylene glycol or glycerol
  • a sugar or sugar alcohol lactic acid, boric acid, or a boric acid derivative, e.g., an aromatic borate ester, or a phenyl boronic acid derivative such as 4-formylphenyl boronic acid
  • a polyol such as propylene glycol or glycerol
  • a sugar or sugar alcohol lactic acid, boric acid, or
  • alkyi groups are sufficiently long to form branched or cyclic chains, the alkyi groups encompass branched, cyclic and linear alkyi chains.
  • the alkyi groups are preferably linear or branched, most preferably linear.
  • the composition preferably comprises a fluorescent agent (optical brightener).
  • fluorescent agents are well known and many such fluorescent agents are available commercially.
  • these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts.
  • Preferred classes of fluorescer are: Di-styryl biphenyl compounds, e.g. Tinopal (Trade Mark) CBS-X, Di-amine stilbene di-sulphonic acid compounds, e.g. Tinopal DMS pure Xtra and Blankophor (Trade Mark) HRH, and Pyrazoline compounds, e.g. Blankophor SN.
  • Di-styryl biphenyl compounds e.g. Tinopal (Trade Mark) CBS-X
  • Di-amine stilbene di-sulphonic acid compounds e.g. Tinopal DMS pure Xtra and Blankophor (Trade Mark) HRH
  • Pyrazoline compounds e.g. Blankophor SN.
  • Preferred fluorescers are: sodium 2 (4-styryl-3-sulphophenyl)-2H-napthol[1 ,2-d]triazole, disodium 4,4'-bis ⁇ [(4-anilino-6-(N methyl-N-2 hydroxyethyl) amino 1 ,3,5-triazin-2- yl)]amino ⁇ stilbene-2-2' disulophonate, disodium 4,4'-bis ⁇ [(4-anilino-6-morpholino-1 ,3,5- triazin-2-yl)]amino ⁇ stilbene-2-2' disulphonate, and disodium 4,4'-bis(2-sulphostyryl)biphenyl.
  • the total amount of the fluorescent agent or agents used in the composition is preferably from 0.0001 to 0.5 wt %, more preferably 0.005 to 2 wt %, most preferably 0.05 to 0.25 wt %.
  • the aqueous solution used in the method has a fluorescer present.
  • the fluorescer is present in the aqueous solution used in the method preferably in the range from 0.0001 g/l to 0.1 g/l, more preferably 0.001 to 0.02 g/l.
  • the composition comprises a perfume.
  • the perfume is preferably in the range from 0.001 to 3 wt %, more preferably 0.05 to 0.5 wt%, most preferably from 0.1 to 1 wt %.
  • CTFA Cosmetic, Toiletry and Fragrance
  • the perfume comprises at least one note (compound) from: alpha-isomethyl ionone, benzyl salicylate; citronellol; coumarin; hexyl cinnamal; linalool; Pentanoic acid, 2- methyl-, ethyl ester; octanal; benzyl acetate; 1 ,6-octadien-3-ol, 3,7-dimethyl-, 3-acetate; cyclohexanol, 2-(1 , 1 -dimethylethyl)-, 1 -acetate; delta-damascone; beta-ionone; verdyl acetate; dodecanal; hexyl cinnamic aldehyde; cyclopentadecanolide; benzeneacetic acid,
  • Useful components of the perfume include materials of both natural and synthetic origin. They include single compounds and mixtures. Specific examples of such components may be found in the current literature, e.g., in Fenaroli's Handbook of Flavor Ingredients, 1975, CRC Press; Synthetic Food Adjuncts, 1947 by M. B. Jacobs, edited by Van Nostrand; or Perfume and Flavor Chemicals by S. Arctander 1969, Montclair, N.J. (USA).
  • compositions of the present invention it is envisaged that there will be four or more, preferably five or more, more preferably six or more or even seven or more different perfume components.
  • top notes are defined by Poucher (Journal of the Society of Cosmetic Chemists 6(2):80 [1955]).
  • Preferred top-notes are selected from citrus oils, linalool, linalyl acetate, lavender, dihydromyrcenol, rose oxide and cis-3-hexanol.
  • Perfume top note may be used to cue the whiteness and brightness benefit of the invention.
  • perfume may be encapsulated, typical perfume components which it is advantageous to encapsulate, include those with a relatively low boiling point, preferably those with a boiling point of less than 300, preferably 100-250 Celsius. It is also
  • perfume ingredients which have a low CLog P (ie. those which will have a greater tendency to be partitioned into water), preferably with a CLog P of less than 3.0.
  • These materials, of relatively low boiling point and relatively low CLog P have been called the "delayed blooming" perfume ingredients and include one or more of the following materials: allyl caproate, amyl acetate, amyl propionate, anisic aldehyde, anisole, benzaldehyde, benzyl acetate, benzyl acetone, benzyl alcohol, benzyl formate, benzyl iso valerate, benzyl propionate, beta gamma hexenol, camphor gum, laevo-carvone, d- carvone, cinnamic alcohol, cinamyl formate, cis-jasmone, cis-3-hexenyl acetate,
  • compositions of the present invention it is envisaged that there will be four or more, preferably five or more, more preferably six or more or even seven or more different perfume components from the list given of delayed blooming perfumes given above present in the perfume.
  • perfumes with which the present invention can be applied are the so-called aromatherapy' materials. These include many components also used in perfumery, including components of essential oils such as Clary Sage, Eucalyptus, Geranium,
  • the laundry treatment composition does not contain a peroxygen bleach, e.g., sodium percarbonate, sodium perborate, and peracid.
  • a peroxygen bleach e.g., sodium percarbonate, sodium perborate, and peracid.
  • the indefinite article “a” or “an” and its corresponding definite article “the” as used herein means at least one, or one or more, unless specified otherwise.
  • the pH of the aqueous liquid laundry detergent composition is preferably from 6.5 to 8.5, most preferably 6.8 to 7.5.
  • the pH may be obtained by the addition of an alkali, such as NaOH, trialkyl amine or an alkanolamine.
  • control base aqueous laundry detergent formulation was made:
  • the EPEI Ethoxylated PolyEthylene Imine
  • the EPEI was a PEI of 600 molecular weight with 20 moles of ethoxylate per NH on the base PEI; it is available as Sokalan HP20 ex BASF.
  • the SRP (Soil Removal Polymer) used was:
  • the SRP is as described in WO2014/019903 (Unilever).
  • the viscosity of the formulation were measured using a Paar Physica MCR300 is a commercial stress rheometer.
  • the formulation was remade with the addition of non-ionic surfactant and alkyl ether carboxylate surfactant. The results are given in the table below.
  • the non-ionic used was a C12-C15 linear alcohol alcohol with 7 moles of ethoxylation).
  • the oleyl ether carboxylate used has 10 moles of ethoxylation.
  • the lauryl ether carboxylate used had 10 moles of ethoxylation.
  • protease Coronase ® ex Novoymes, Bagsvaerd, Danmark
  • amylase Novalase ® ex Novoymes, Bagsvaerd, Danmark

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  • 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)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

La présente invention concerne un polymère de polyéthylène-imine alcoxylé et une formulation de tensioactif à utiliser avec du linge domestique.
PCT/EP2017/053800 2016-04-08 2017-02-20 Composition de détergent à lessive WO2017174252A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP17708995.0A EP3440170B1 (fr) 2016-04-08 2017-02-20 Composition de détergent pour lessive
CN201780020519.8A CN109072131A (zh) 2016-04-08 2017-02-20 洗衣洗涤剂组合物
BR112018070472-5A BR112018070472B1 (pt) 2016-04-08 2017-02-20 Composição de detergente líquida aquosa para lavagem de roupas e método doméstico de tratamento de um tecido

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EP16164555 2016-04-08
EP16164555.1 2016-04-08

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CN (1) CN109072131A (fr)
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018206202A1 (fr) * 2017-05-10 2018-11-15 Unilever Plc Composition de détergent à lessive
WO2020260006A1 (fr) * 2019-06-28 2020-12-30 Unilever Plc Compositions détergentes
EP3833730B1 (fr) 2018-08-10 2022-02-16 Unilever Global Ip Limited Détergent
WO2022063708A1 (fr) 2020-09-24 2022-03-31 Unilever Ip Holdings B.V. Composition
US20220372397A1 (en) * 2019-06-28 2022-11-24 Conopco, Inc., D/B/A Unilever Detergent composition
US20220372400A1 (en) * 2019-06-28 2022-11-24 Conopco, Inc., D/B/A Unilever Detergent composition

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023067073A1 (fr) * 2021-10-21 2023-04-27 Unilever Ip Holdings B.V. Compositions détergentes

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5269960A (en) * 1988-09-25 1993-12-14 The Clorox Company Stable liquid aqueous enzyme detergent
US6090768A (en) * 1998-06-10 2000-07-18 Reckitt & Colman Inc. Germicidal liquid laundry detergent compositions including optical brighteners
WO2013087284A1 (fr) * 2011-12-12 2013-06-20 Unilever Plc Compositions pour lessiver
WO2014060235A2 (fr) * 2012-10-17 2014-04-24 Unilever Plc Compositions détergentes pour le linge

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2880074B1 (fr) * 2012-07-31 2016-06-29 Unilever Plc. Compositions alcalines de détergent liquide pour la lessive comprenant des polyesters
CN108884415A (zh) * 2016-03-21 2018-11-23 荷兰联合利华有限公司 洗衣洗涤剂组合物

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5269960A (en) * 1988-09-25 1993-12-14 The Clorox Company Stable liquid aqueous enzyme detergent
US6090768A (en) * 1998-06-10 2000-07-18 Reckitt & Colman Inc. Germicidal liquid laundry detergent compositions including optical brighteners
WO2013087284A1 (fr) * 2011-12-12 2013-06-20 Unilever Plc Compositions pour lessiver
WO2014060235A2 (fr) * 2012-10-17 2014-04-24 Unilever Plc Compositions détergentes pour le linge

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018206202A1 (fr) * 2017-05-10 2018-11-15 Unilever Plc Composition de détergent à lessive
CN110914397A (zh) * 2017-05-10 2020-03-24 荷兰联合利华有限公司 洗衣洗涤剂组合物
EP3622047B1 (fr) 2017-05-10 2020-12-16 Unilever PLC, a company registered in England and Wales under company no. 41424 of Composition détergente liquide pour le lavage
CN110914397B (zh) * 2017-05-10 2021-04-13 荷兰联合利华有限公司 洗衣洗涤剂组合物
EP3833730B1 (fr) 2018-08-10 2022-02-16 Unilever Global Ip Limited Détergent
WO2020260006A1 (fr) * 2019-06-28 2020-12-30 Unilever Plc Compositions détergentes
US20220372397A1 (en) * 2019-06-28 2022-11-24 Conopco, Inc., D/B/A Unilever Detergent composition
US20220372400A1 (en) * 2019-06-28 2022-11-24 Conopco, Inc., D/B/A Unilever Detergent composition
WO2022063708A1 (fr) 2020-09-24 2022-03-31 Unilever Ip Holdings B.V. Composition

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BR112018070472B1 (pt) 2023-04-18
EP3440170A1 (fr) 2019-02-13
BR112018070472A2 (pt) 2019-01-29
AR108173A1 (es) 2018-07-25
EP3440170B1 (fr) 2020-04-08
CN109072131A (zh) 2018-12-21

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