CN105745314A - Laundry compositions - Google Patents
Laundry compositions Download PDFInfo
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- CN105745314A CN105745314A CN201480064997.5A CN201480064997A CN105745314A CN 105745314 A CN105745314 A CN 105745314A CN 201480064997 A CN201480064997 A CN 201480064997A CN 105745314 A CN105745314 A CN 105745314A
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
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- 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
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
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- 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
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
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- Oil, Petroleum & Natural Gas (AREA)
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- Health & Medical Sciences (AREA)
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- Detergent Compositions (AREA)
Abstract
The invention is directed to liquid laundry compositions containing (a) surfactant, (b) a fabric softening anionic silicone, and, (c) a cationic polymer, wherein the anionic group(s) on the fabric softening anionic silicone are not located on a terminal position on the longest linear silicone chain, wherein the weight ratio of the silicone to the cationic polymer is from 5:1 to 1 :1, and wherein the liquid detergent composition has a pH of from 6 to 10; and to the use of said composition to soften fabrics.
Description
Invention field
The present invention relates to laundry composition.The laundry composition softened is carried out more particularly it relates to be in the suds.
Background of invention
Laundry detergent has been adopted to clean textile fabric traditionally, including medicated clothing.After the washing, fabric is likely to generally make us feeling coarse.In order to prevent this point, coarse particularly in what experience after multiple cycles of washing, the technology that has been developed over is to increase the pliability of fabric, including the conditioner composition added when rinsing and the softening system being added into composition of detergent.
Fabric-softening polysiloxanes has been used for being provided pliability by laundry detergent composition for fabric.But, in unacceptable turbid mixed (haze), the problem that there is preparation stability.
Summary of the invention
In the first aspect, the present invention relates to liquid laundry detergent compositions, it comprises:
The surfactant of (a) 5 to 40wt.%；
The fabric-softening anion polysiloxane of (b) 0.05 to 5wt.%；With
The cationic polymer of (c) 0.05 to 2.5wt.%,
Wherein the anionic group on fabric-softening anion polysiloxane (one or more) is not on the end position on the linear silicones chain grown most.
Wherein polysiloxanes is 5:1 to 1:1 with the weight ratio of cationic polymer；Further, wherein liquid detergent composition has the pH of 6 to 10.
Preferably, the anionic group on fabric-softening anion polysiloxane (one or more) is positioned at from least 5, the end position on the longest linear silicones chain Si atom.
Preferably, anion polysiloxane has 1,000 to 100,000, more preferably 2, and 000 to 50,000, even more preferably from 5,000 to 50,000, most preferably 10, the molecular weight of 000 to 50,000.Preferably, anion polysiloxane has the anionic group content of at least 1mol%, preferred 2mol%.
Preferably, anion polysiloxane includes carboxyl polysiloxanes.
Preferably, by polysiloxanes in the form of an emulsion, more preferably with the form of non-ionic emulsion, be added into preparation most preferably with branched nonionic emulsifying agent.
Preferably, the pH of liquid detergent composition is that pH6.5 to 9.5, most preferably pH7 are to 9, for instance for pH7.5 to 8.5.
The preferred levels of cationic polymer is 0.1 to 2wt.%, more preferably 0.1 to 1wt.%, most preferably 0.1 to 0.75wt.%；And the preferred levels of anion polysiloxane is to exist with the level of 0.1 to 2.5wt.%, preferably 0.1 to 2wt.%.
Preferably, cationic polymer is Cationic polysaccharide polymer.
Preferred Cationic polysaccharide polymer is cation guar gum and cationic cellulose polymer.It particularly preferably is the hydroxyether cellulosic (i.e. quaternised hydroxyethyl cellulose) modified by introducing cation group.
Optionally but preferably, described compositions comprises the composition selected from fatty acid or its salt, dope dye (shadingdye), enzyme, antiredeposition polymer, dye transfer inhibiting polymers, builder, chelating agen, opacifier (sunscreen), fluorescent agent, aromatic (perfume) and/or soil release polymer further.
In second aspect, the invention provides the purposes for softening fabrics of the compositions according to the first aspect of the invention.
Detailed Description Of The Invention
As used herein, term " comprising " represent include (including), by ... constitute (madeupof), by ... form (composedof), by ... composition (consistingof) and/or substantially by ... composition (consistingessentiallyof).
Unless otherwise stated, all percentage ratios of citation are wt.%, based on the total amount in laundry composition.
The present invention relates to the laundry composition comprising surfactant, cationic polymer and fabric-softening anion polysiloxane, wherein the anionic group on fabric-softening anion polysiloxane (one or more) is not on the end position of polysiloxanes.
The form of the present invention
The present invention can be adopted as any one (such as gel and waterborne liquid) in the various ways of liquid laundry compositions.Preferably, they are that master washes (mainwash) product.It can adopt can be the dilutable or not dilutable form for the main laundry composition washed.Laundry composition can be such as isotropic liquid or surfactant-structured liquid.The particularly preferred form of the present invention includes the product of composition, detergent/softening agent, to provide " be in the suds and soften ".
Preferably, the pH of liquid detergent composition is that pH6.5 to 9.5, most preferably pH7 are to 9, for instance pH7.5 to 8.5.
Surfactant
Composition of detergent comprises surfactant.
Preferably, this surfactant includes nonionic surfactant and anion surfactant.
If it does, nonionic surfactant preferably includes alcohol ethoxylate.
Alcohol ethoxylate is formed by the reaction of primary alconol or secondary alcohol and oxirane.Generally, aliphatic series C is made8To C18Primary or secondary linear or branched alcohols with ethylene oxide is to produce the mole reaction needed for alcohol ethoxylate.Preferred alcohol ethoxylate have 2 to 40, preferably 3 to 30, more preferably 5 to 20 be connected to the ethylene oxide unit of aliphatic chain.
Surfactant can be selected from " SurfaceActiveAgents ", rolls up 1, Schwartz&Perry, Interscience1949, volume 2, Schwartz, Perry&Berch, Interscience1958, " McCutcheon'sEmulsifiersandDetergents " latest edition published by ManufacturingConfectionersCompany or " Tenside-Taschenbuch ", H.Stache, the second edition, CarlHauserVerlag, the surfactant described in 1981.Preferably, the surfactant of use is saturated.
Operable suitable nonionic detergent compounds is particularly including the product with the hydrophobic group compound (such as aliphatic alcohol, acid, amide or alkyl phenol) with hydrogen atoms and alkylene oxide (especially independent oxirane or the oxirane together with expoxy propane).Specific nonionic detergent compounds is C6To C22Alkylphenol-ethylene oxide condensate, is generally 5 to 25 EO of per molecule, i.e. 5 to 25 ethylene oxide units, and aliphatic series C8To C18The condensation product of primary or secondary linear or branched alcohols with ethylene oxide, is generally 5 to 40 EO.
Operable suitable anionic detergent compounds can be the water-soluble alkali metal salts of organo-sulfate and sulphonic acid ester; described organo-sulfate and sulphonic acid ester have the alkyl comprising about 8 to about 22 carbon atoms, and term alkyl is for including the moieties of higher acyl.The example of suitable synthetic anionic detergent compound is alkyl sodium sulfate and potassium, especially by the senior C that sulphation is such as produced by fatty oil or Oleum Cocois8To C18Those of alcohol acquisition, alkyl C9To C20Benzene sulfonic acid sodium salt and potassium, particularly linear secondary alkyl C10To C15Benzene sulfonic acid sodium salt；And alkyl glyceryl ether sulphates, the especially ether of those higher alcohols derived from fatty oil or Oleum Cocois and the synthol derived from oil.Preferred anionic detergent compounds is C11To C15Sodium alkyl benzene sulfonate and C12To C18Alkyl sodium sulfate.The salt of the sulphonic acid ester comprised as hydrotropic agent (hydrotrobe) can be considered as anion surfactant as defined herein extraly.Be also applicable to be such as described in EP-A-328177 (Unilever) demonstrate resistance to those saltouing surfactant, at the alkyl polyglucoside surfactant described in EP-A-070074, and alkyl monoglycosides.
The total amount of the surfactant existed in the composition is 5 to 40wt.%.This surfactant level is preferably at least 6wt.%, more preferably at 10wt.%.It is highly preferred that the total amount of surfactant is 12.5 to 40wt.%, preferably 15 to 35wt.%.
Preferred surfactant system includes anion and nonionic surfactant.
Nonionic detergent preferably exists with the amount of 2 to 40wt.%, preferably 5 to 35wt.%, more preferably 6 to 20wt.%.
Preferred nonionic surfactant is the C of the ethoxylation (ethoxylation) with average 7 to 9 moles12To C15Alkyl chain.
Anion surfactant preferably exists with the amount of 4 to 40wt.%, preferably 5 to 35wt.%, more preferably 6 to 20wt.%.
Preferred anion surfactant is: linear alkylbenzene sulfonate (LAS), have the lauryl ether sodium sulfonate of the ethoxylation of 1 to 3 mole (on average), primary alkyl sulfonate, methyl ether sulfate and secondary alkyl sulfonate or its mixture.
For the purpose of the level explaining the surfactant existed in the formulation, the level of surfactant does not include fatty acid and their salt.
Except aforesaid nonionic and anion surfactant, it is also possible to there is other surfactant, for instance both sexes, amphion and cationic surfactant.
Fabric-softening anion polysiloxane
Polysiloxanes and their chemical property are described in such as TheEncyclopediaofPolymerScience, and the 11st volume, in the 765th page.
Described compositions comprises the fabric-softening anion polysiloxane of the level with 0.05 to 5wt.%, preferably 0.1 to 2.5wt.%, more preferably 0.1 to 2wt.%.
The example of fabric-softening anion polysiloxane is introduced into the polysiloxanes of carboxyl, sulfuric ester, sulfo group (sulphonic), phosphate ester and/or phosphonate ester degree of functionality (functionality).
Preferred anion polysiloxane is carboxy-functionalized polysiloxanes.
For the present invention disclosed herein, anion polysiloxane can acid or the form of anion.Such as carboxy-functionalized polysiloxanes, it can exist with the form of carboxylic acid or carboxylate anion.
One example of commercially available material is: from the X22-3701E of ShinEtsu.
Preferably, anion polysiloxane has 1,000 to 100,000, more preferably 2, and 000 to 50,000, even more preferably from 5,000 to 50,000, most preferably 10, the molecular weight of 000 to 50,000.
Preferably, anion polysiloxane has the anionic group content of at least 1mol%, preferred 2mol%.
Anionic group (one or more) on fabric-softening anion polysiloxane is not on the end position of linear silicones chain grown most.
This represents that described compositions comprises anion polysiloxane, and wherein anionic group is positioned at except the somewhere except the end of polysiloxane chain.Term " end position " and " end at polysiloxane chain " are for showing not find anionic functionality in the terminal (terminus) of the longest linear silicones chain.
When polysiloxanes is straight chain character, then they have 2 ends.Fabric-softening anion polysiloxane used herein comprises the anionic group on the end position being not at polysiloxanes.
Some polysiloxanes are side chain character.When for this situation, term " end position " and " end at polysiloxane chain " do not find anionic functionality for showing in the terminal of the longest linear silicones chain.
Those of the anionic group of the chain middle position that preferred anion polysiloxane is included on poly-silica.It is therefore preferred that the anionic group (one or more) on fabric-softening anion polysiloxane is positioned at from least 5, the end position on the longest linear silicones chain Si atom.
Preferably, the anionic group on fabric-softening anion polysiloxane (one or more) is positioned at from least 5, the end position on the longest linear silicones chain Si atom.
Preferably, polysiloxanes is added into preparation in the form of an emulsion, more preferably with the form of non-ionic emulsion.It is highly preferred that this emulsion is prepared by nonionic emulsifier, more preferably branched nonionic emulsifying agent such as EcosurfEH-3 (DowChemical) or Berol840 (AkzoNobel).
The weight ratio of polysiloxanes and cationic polymer is 5:1 to 1:1.
Cationic polymer
Described compositions comprises cationic polymer with the level of 0.05 to 2.5wt.%, preferably 0.1 to 2wt.%, more preferably 0.1 to 1wt.%, most preferably 0.1 to 0.75wt.%.
This term refers to the polymer with overall positive charge.
Preferably, cationic polymer is selected from: Cationic polysaccharide polymer, glycopolymers non-with the cation with cationic protonated amine or quaternary ammonium functionality, the non-glycopolymers of described cation is derived from comprising homopolymer or the copolymer of the monomer of amino or quaternary nitrogen functional group, and it is polymerized by least one in following monomeric species: acrylate, methacrylate, acrylamide, Methacrylamide；Allylic (includes diallyl and methacrylic)；Aziridine (ethyleneimine)；And/or vinyl monomer kind, and mixture.
More preferably, cationic polymer is selected from the polymer of cationic cellulose polymer, cationic guar polymer, cation quaternary diallyl ammonium, (methyl) acrylate, (methyl) acrylic acid diethylamino ethyl ester or (methyl) tbutylaminoethylacrylate are with their quaternary amine or the homopolymer of protonated amines form or copolymer, and mixture.
Most preferably, cationic polymer is Cationic polysaccharide polymer.
It is highly preferred that Cationic polysaccharide polymer is cation guar gum or cationic cellulose polymer.Most preferably, cationic polymer is cationic cellulose polymer, for instance quaternised hydroxyethyl cellulose.
Described compositions can comprise single cationic polymer or the mixture of the cationic polymer from identical or different kind, and namely said composition can comprise Cationic polysaccharide polymer and the non-polysaccharide polymer of cation.The suitable non-polysaccharide polymer of commercial cation preferably but not exclusively takes from those in Polyquarternium series, being such as Polyquat5,6,7,11,15,16,28,32,37 and 46, it is commercially available with Flocare, Merquat, Salcare, Mirapol, Gafquat and Luviquat trade name.The non-polysaccharide of cation can be used when not following polyquaternary ammonium salt (Polyquaterium) nomenclature.
Cationic polysaccharide polymer
Term " Cationic polysaccharide polymer " refers to the polymer with polysaccharide skeleton and overall positive charge.The polymer that polysaccharide is made up of the monosaccharide monomers linked together by glycosidic bond.
The cationic polymer based on polysaccharide existed in the present compositions has modified polysaccharide skeleton, and modified some free hydroxyl groups being in that to make extra chemical group and polysaccharide skeleton react modified cellulose monomer units is provided overall positive charge.
Being suitable for the preferred kind of the Cationic polysaccharide polymer of the present invention is those of the polysaccharide skeleton that has and be modified to introduce quaternary ammonium salt.Preferably, quaternary ammonium salt is connected to polysaccharide skeleton by ethoxy or hydroxypropyl.Preferably, the charged nitrogen of quaternary ammonium salt has one or more alkyl substituent.
Preferably the cationic polymer based on polysaccharide has based on guar gum or based on cellulosic skeleton.It is most preferred based on cellulosic cationic polymer.
Guar gum is the galactomannan with the mannose backbone that β-Isosorbide-5-Nitrae connects, and described skeleton has to α-1, the branch point of 6 galactose units connected.
Suitable cationic guar derivative, such as guar hydroxypropyltrimonium ammonium chloride, its instantiation includes the Jaguar series available commercially from Rhone-PoulencIncorporated and the N-Hance series available commercially from AqualonDivisionofHercules, Inc.
The example being preferably based on the cationic polymer of guar gum is guar gum 2-hydroxyl-3-(trimethyl ammonium) propyl ether salt.
Cellulose is the polysaccharide having glucose as monomer whose, and it is the straight chain polymer of the D-glucopyranose units connected via β-Isosorbide-5-Nitrae glycosidic bond especially, and is the polymer of linear non-branching.
Example cationic cellulose polymer is the salt of the epoxide reactive hydroxyethyl cellulose replaced with trimethyl ammonium, it is called polyquaternary ammonium salt 10 (Polyquatemium10) according to the international nomenclature of cosmetic composition in the art, and available commercially from AmercholCorporation (subsidiary of TheDowChemicalCompany), the polymer as PolymerLR and JR series is commercially available.Other polymer is commercially available by TheDowChemicalCompany with SoftCAT trade name.Other suitable type of cationic cellulose includes the polymeric quaternary ammonium salts of the epoxide reactive hydroxyethyl cellulose replaced with lauryl dimethyl ammonium, and it is called polyquaternary ammonium salt 24 according to the international nomenclature of cosmetic composition in the art.
The representative instance of preferred cationic cellulose polymer includes coco dimethyl ammonium hydroxypropyl oxygen ethyl cellulose, Lauryldimonium Hydroxypropyl base oxygen ethyl cellulose, ammonium chloride hydroxypropyl oxygen ethyl cellulose and ammonium chloride hydroxyethyl cellulose；Cellulose 2-ethoxy 2-hydroxyl 3-(trimethyl ammonium) propyl ether salt (cellulose2-hydroxyethyl2-hydroxy3-(trimethylammonio) propylethersalt), polyquaternary ammonium salt-4, Polyquaternium-10, polyquaternary ammonium salt-24 and Polyquaternium-67, or its mixture.
It is highly preferred that cationic cellulose polymer is quaternised hydroxyether cellulosic cationic polymer.These are commonly called Polyquaternium-10.Commercially available with trade name UCARE by TheDowChemicalCorporation for suitable commercial cationic cellulose polymer product used according to the invention.
Other cationic polymerization species
The cationic polymer based on non-polysaccharide can also be used.The non-glycopolymers of suitable cation includes having those of cationic protonated amine or quaternary ammonium functionality, the non-glycopolymers of described cation is derived from comprising homopolymer or the copolymer of the monomer of amino or quaternary nitrogen functional group, and it is polymerized by least one in following monomeric species: acrylate, methacrylate, acrylamide, Methacrylamide；Allylic (includes diallyl and methacrylic)；Aziridine；And/or vinyl monomer kind, and mixture.
The non-glycopolymers of preferred cation includes the polymer of cation quaternary diallyl ammonium with (methyl) acrylate, (methyl) acrylic acid diethylamino ethyl ester or (methyl) tbutylaminoethylacrylate with their quaternary amine or the homopolymer of protonated amines form or copolymer, and mixture.
Other the suitable cationic polymer used in the composition includes l-vinyl-2-pyrrolidone and the copolymer (being referred to as polyquaternary ammonium salt-16) of 1-vinyl-3-methylimidazole salt；The copolymer (being referred to as polyquaternary ammonium salt-11) of l-vinyl-2-pyrrolidone and dimethylaminoethyl methacrylate；The polymer of cation quaternary diallyl ammonium, including the copolymer (being known respectively as polyquaternary ammonium salt 6 and polyquaternary ammonium salt 7) of such as dimethyl diallyl ammonium chloride homopolymer, acrylamide and dimethyl diallyl ammonium chloride；Acrylic acid ampholyte copolymer, including the terpolymer (being referred to as polyquaternary ammonium salt 39) of the copolymer (being referred to as polyquaternary ammonium salt 22) of acrylic acid and dimethyl diallyl ammonium chloride, acrylic acid and dimethyl diallyl ammonium chloride and acrylamide, and the terpolymer of acrylic acid and Methacrylamide hydroxypropyltrimonium chloride and methacrylate (being referred to as polyquaternary ammonium salt 47).
The monomer that preferred cation replaces is dialkyl amido pi-allyl acrylamide (dialkylaminoallcylacrylamide), dialkyl amido allyl methacrylamide (dialkylaminoallcylmethacrylamide) and the combination thereof that cation replaces.
The counter ion counterionsl gegenions of cationic polymer are freely selected from following halogen ion: chloride ion, bromide ion and iodide ion；Or selected from hydroxyl, phosphate radical, sulfate radical, bisulfate ion, ethyl sulphate, methylsulfate, formate and acetate.
Many aforesaid cationic polymers can synthesize with many different molecular weights and be purchased.Preferably, the molecular weight of cationic polymer is 10,000 to 2,000,000 dalton, more preferably 100,000 to 1,000,000 dalton, even more preferably from 250,000 to 1,000,000 dalton.
Optional member
Composition of detergent can optionally comprise one or more in following optional member: fatty acid or its salt, dope dye, enzyme, antiredeposition polymer, dye transfer inhibiting polymers, builder, chelating agen, opacifier, fluorescent agent, aromatic, and/or soil release polymer.
Fatty acid
Described compositions can also comprise fatty acid or soap, for instance soap.Example includes C6-C22Fatty acid and sodium salt, potassium salt and ammonium salt.For the purpose of the level explaining the surfactant existed in the formulation, the level of surfactant does not include fatty acid and their salt.
Fatty acid exists with the level of 0.25 to 12wt.%, preferably 0.5 to 10wt.%.
Builder and chelating agen
Composition of detergent can also optionally comprise Organic detergent builders or the chelating agen material of low relative levels.Example includes alkali metal, citrate, succinate, malonate, carboxymethyl succinates, carboxylate, multi-carboxylate and many acetyl group carboxylate (polyacetylcarboxylate).Instantiation includes oxygen disuccinic acid, mellic acid., benzene polycarboxylic acid, ethylenediaminetetraacetic acid, DTPA, alkyl-or the sodium salt of alkenyl succinic acid, nitrilotriacetic acid(NTA) and citric acid, potassium salt and lithium salts.Other example is DEQUESTTM, Thermophos the organic phospho acid salt form chelating agen sold, and alkane hydroxyethylidene diphosphonic acid salt (alkanehydroxyphosphonate).
Other suitable organic washing-assisting detergent includes polymer and the copolymer of the known higher molecular weight with builder capacity.Such as, such material includes suitable polyacrylic acid, poly, and poly propenoic acid maleic acid and their salt, for instance by BASF with title SOKALANTMThose sale.Another kind of suitable builder is sodium carbonate.
If used, builder material can account for about 0.5% to the 20wt% of described compositions, preferred 1wt% to 10wt%.Preferred builder level is less than the 10wt% of described compositions and is preferably smaller than 5wt%.
Preferably, laundry wash agent formulation is that phosphate free helps the laundry wash agent formulation washing (built), namely comprises less than the phosphate of 1wt.%.
Dope dye
Dope dye deposits to fabric during the washing or rinse step of washing process, provides visible chrominance (hue) for fabric.Hobby according to consumer, it is possible to complete the toning to white garments by any color.Blue and purple is particularly preferred tone, and it is therefore preferable that the mixture of dyestuff or dyestuff is to provide those of blueness or violet hue in white fabrics.The dope dye used is blueness or purple preferably.
Dope dye chromophore is preferably selected from: monoazo, bisazo, triphenyl methane, three benzodiazines (triphenodioxazine), phthalocyanine, naphthalene lactams, azine and anthraquinone.Most preferably monoazo, bisazo, azine and anthraquinone.
Most preferably, dyestuff is with at least one sulfonate group (sulfonategroup).
Preferred dope dye is selected from direct dyes, acid stain, hydrophobic dye, the dye of positive ion and reactive dye (reactivedye).
If comprised, dope dye is to be present in described compositions with 0.0001 to 0.01wt%.
Fluorescent agent
Described compositions preferably comprises fluorescent agent (fluorescent whitening agent).Fluorescent agent is known, and many such fluorescent agents are commercially available.Generally, these fluorescent agents are the alkali metal salts with them, for instance the form of sodium salt is supplied and uses.The total amount of the fluorescent agent (one or more) used in the composition is generally 0.005 to 2wt.%, more preferably 0.01 to 0.1wt.%.The preferred kind of fluorescent agent is: two-styrylbiphenyl compounds, such as Tinopal (trade mark) CBS-X, two-amine stilbene two-sulfoacid compound, for instance TinopalDMSpureXtra and Blankophor (trade mark) HRH, and pyrazoline compounds, for instance BlankophorSN.Preferred fluorescent agent is: 2-(4-styryl-3-sulfo group phenyl)-2H-naphthols [1, 2-d] 1-Sodium-1,2,4-Triazole (sodium2-(4-styryl-3-sulfophenyl)-2H-napthol [1, 2-d] trazole), 4, double, two { [(4-anilino--6-(N-methyl-N-2-ethoxy) amino-1 of 4'-, 3, 5-triazine-2-base)] amino } stilbene-2-2' disulfonate, 4, double, two { [(4-anilino--6-the morpholinyl-1 of 4'-, 3, 5-triazine-2-base)] amino } stilbene-2-2' disulfonate, with 4, double, two (2-sulfostyryl) the biphenyl disodium of 4'-.
Aromatic
Preferably, described compositions comprises aromatic.Aromatic is preferably 0.001 to 3wt.%, most preferably 0.1 to 1wt.%.The many suitable example of aromatic provides in CTFA (Cosmetic, the ToiletryandFragranceAssociation) 1992InternationalBuyersGuide published by CFTAPublications and the OPD1993ChemicalsBuyersDirectory80thAnnualEdition published by SchnellPublishingCo.
Commonly multiple fragrance components is present in preparation.In the present compositions, it is contemplated that will there is four kinds or more, preferably five kinds or more, more preferably six kinds or more or even seven kinds or more different fragrance components.
In fragrance blend, it is preferable that 15 to 25wt.% is head fragrant (topnote).Head is fragrant by Poucher defined (JournaloftheSocietyofCosmeticChemists6 (2): 80 [1955]).Preferred head perfume (or spice) is selected from tangerine oil, linalool, linalyl acetate, lavandula angustifolia, dihydromyrcenol, rose oxide and cis-3-hexanol.
Preferably laundry treatment compositions does not comprise peroxygen bleach, for instance SODIUM PERCARBONATE, Dexol and peracid.
Polymer
Described compositions can comprise one or more polymer.By helping the transfer making dirt scattered (retail) and/or prevention dyestuff in solution or suspension, polymer can help to cleaning process.Polymer can also contribute to decontamination process.Describe dye transfer, antiredeposition and soil release polymer in further detail below.
Described compositions can comprise one or more polymer.Example is carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, PEG, poly-(vinyl alcohol), ethoxylated polyamine, polycarboxylate such as polyacrylate, maleic acid/acrylic copolymer and lauryl methacrylate/acrylic copolymer.
Dye transfer inhibitor
Modern detergent compositions generally uses polymer as so-called " dye transfer inhibitor ".These polymer prevent the migration of dyestuff, especially during long soak time.Generally, such dye transfer inhibitor includes polyvinylpyrrolidonepolymers polymers, polyamines N-oxide polymer, NVP and the copolymer of N-vinyl imidazole, manganese phthalocyanine, peroxidase, and mixture, and it generally exists with the level of 0.01 to the 10wt.% of the total amount based on laundry composition.
Antiredeposition polymer
Antiredeposition polymer is designed to suspend or dispersion dirt.Typically, antiredeposition polymer is ethoxylation and/or propoxylated polyethylene imine or polycarboxylate/salt material, such as based on acrylic acid homopolymer or copolymer, its can trade mark ACUSOL available from DowChemical, with Alcosperse available from Akzonobel or with Sokolan available from BASF.
Soil release polymer
The example of suitable soil release polymer includes gathering (vinyl esters), for instance C1-C6The graft copolymer of vinyl esters, it is preferable that be grafted to poly-(vinyl acetate) on polyalkylene oxide backbones.This kind of commercially available detergent includes the material of SOKALAN type, for instance SOKALANHP-22, and it is available from BASF (Germany).Other suitable soil release polymer different types of includes commercially available material ZELCON5126 (from DuPont) and MILEASET (from ICI).If it does, soil release polymer can be comprised based on the level of 0.01 to the 10wt.% of the total amount in laundry composition.Other example of soil release polymer is terephthalic acid/diol copolymer, and it is sold with trade name Texcare, Repel-o-tex, Gerol, Marloquest, Cirrasol.
Hydrotropic agent
If being the form of liquid, then liquid detergent composition can optionally comprise hydrotropic agent, and it can stop Formation of liquid crystals.Therefore, hydrotropic it is added with the clarification that helps compositions/transparent.Suitable hydrotropic agent includes but not limited to propylene glycol, ethanol, glycerol, urea, benzene sulfonate, toluene fulfonate, xylenesulfonate or cumene sulfonate.Suitable salt includes but not limited to sodium, potassium, ammonium, monoethanolamine, triethanolamine.Sulfonate may be considered as anion surfactant as defined herein.Preferably, hydrotropic agent is selected from propylene glycol, xylenesulfonate, ethanol and urea to provide optimum performance.Hydrotropic amount is generally 0 to 30%, preferably 0.5 to 30%, more preferably 0.5 to 30%, most preferably 1 to 15%.
Enzyme
Enzyme can also be present in preparation.Preferred enzyme includes protease, lipase, pectin lyase, amylase, at, cellulase, mannase.If it does, can with known enzyme stabilizers, for instance boric acid makes described enzyme stable.
Embodiment
Prepare following base formulation A-F, and be shown in Table 1.These demonstrate the compositions having across the level of a series of component and the surfactant system of ratio.
Table 1
| A | B | C | D | E | F | |
| Neodol 25-7 | 6.28 | 2.51 | 12.52 | 7.63 | 18.76 | 11.28 |
| LAS acid | 13.04 | 5.16 | 8.52 | 5.07 | 4.31 | 2.87 |
| SLES 3EO | 8.71 | 3.57 | 6.01 | 3.56 | 3.01 | 1.39 |
| Propylene glycol | 15.00 | 15.00 | 15.00 | 15.00 | 15.00 | 15.00 8 --> |
| Fatty acid | 2.51 | 1.00 | 2.51 | 1.51 | 2.00 | 1.51 |
| Cationic polymer (LR400) | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 |
| Triethanolamine | 2.44 | 0.80 | 2.52 | 1.53 | 2.53 | 1.49 |
| Aromatic | 1.00 | 1.00 | 1.00 | 1.00 | 1.00 | 1.00 |
| Proxel GXL | 0.11 | 0.11 | 0.11 | 0.11 | 0.11 | 0.11 |
| Reactive polysiloxanes | 1 | 1 | 1 | 1 | 1 | 1 |
| NaOH (to pH) | 8-8.5 | 8-8.5 | 8-8.5 | 8-8.5 | 8-8.5 | 8-8.5 |
| Water | To 100 | To 100 | To 100 | To 100 | To 100 | To 100 |
The method preparing preparation
In ambient temperature (about 22oC), under, use Janke&KunkelIKARW20 overhead type stirrer, with the shear rate of 150rpm, water and hydrotropic agent are mixed 2-3 minute.Before adding surfactant and fatty acid, add salt and alkali matter (alkalis) and mix 5 minutes.Slight heat release will be shown at this azeotropic mixture.< after 30 ° of C, add cationic polymer (LR400 added as an aqueous solution) solution and any remaining ingredient, such as aromatic, preservative, dyestuff and polysiloxanes allowing to cool to.Add described polysiloxanes with 1wt.%, and it is added in the form of an emulsion.
Test 4 kinds of polysiloxanes, the PDMS of a kind of standard and 3 kinds of anion polysiloxanes from Shin-Etsu:
·100CstPDMS(‘X’)
The carboxyl polysiloxanes that X22-3710E (1) chain is intermediate modified, it has vertically or pendant is in the carboxyl of main silicone matrix
X22-162C (' Y ') both-end carboxyl polysiloxanes, it has the carboxyl at each end position place at main silicone matrix
X22-3710 (' Z ') monofocal end carboxyl polysiloxanes, it has the carboxyl at an end position place at main silicone matrix
Polysiloxanes 1 is according to the present invention, and polysiloxanes X, Y and Z are as a comparison.
Stability/turbid mixed measurement
4 kinds of polysiloxanes are formulated in every kind in 6 kinds of preparations (A-F).Fetch the sample from every kind of preparation and add it to 1cm cuvette, and being measured by UV-Vis, taking the reading under 500nm.This UV-Vis measurement provides the turbid mixed level of product.Relatively low reading shows less turbid mixed.
Table 2
| Preparation | Polysiloxanes X | Polysiloxanes 1 | Polysiloxanes Y | Polysiloxanes Z |
| A | 0.574 | 0.067 | 0.218 | Unstable |
| B | 1.346 | 0.074 | 1.283 | Unstable |
| C | 0.817 | 0.058 | 0.475 | Unstable |
| D | 1.630 | 0.038 | 1.813 | Unstable |
| E | 0.903 | 0.025 | 0.490 | Unstable |
| F | 1.715 | 0.434 | 1.661 | Unstable |
Result from table 2, be clear that compared to non-anion polysiloxane (polysiloxanes X) and the anion polysiloxane (polysiloxanes Y and Z) with terminal anionic group, functionalized by anion substituent in the middle of chain and do not comprise in addition the anion polysiloxane (polysiloxanes 1) of terminal anionic polysiloxane group reduce turbid mixed in demonstrate best stability.
Claims (11)
1. liquid laundry detergent compositions, it comprises:
The surfactant of (a) 5 to 40wt.%；
The fabric-softening anion polysiloxane of (b) 0.05 to 5wt.%；With
The cationic polymer of (c) 0.05 to 2.5wt.%,
Wherein the one or more anionic groups on fabric-softening anion polysiloxane are not on the end position on the linear silicones chain grown most；With
Wherein liquid detergent composition has the pH of 6 to 10.
2. compositions according to claim 1, wherein said one or more anionic groups on fabric-softening anion polysiloxane are positioned at from least 5, the end position on the longest linear silicones chain Si atom.
3. the compositions according to any one of claim 1 or claim 2, wherein said anion polysiloxane has 1,000 to 100,000, preferably 2, and 000 to 50,000, even more preferably from 5,000 to 50,000, most preferably 10, the molecular weight of 000 to 50,000；And/or described anion polysiloxane has the anionic group content of at least 1mol%, preferred 2mol%.
4. the compositions according to aforementioned any one of claim, wherein said anion polysiloxane includes carboxyl polysiloxanes.
5. the compositions according to aforementioned any one of claim, is wherein added into preparation by described polysiloxanes with emulsion, preferred non-ionic emulsion, the more preferably form of use branched nonionic emulsifying agent.
6. the compositions according to aforementioned any one of claim, the pH of wherein said liquid detergent composition is that pH6.5 to 9.5, most preferably pH7 are to 9, for instance for pH7.5 to 8.5.
7. the compositions according to aforementioned any one of claim, wherein said cationic polymer exists with the level of 0.1 to 2wt.%, preferably 0.1 to 1wt.%, more preferably 0.1 to 0.75wt.%；And described anion polysiloxane exists with the level of 0.1 to 2.5wt.%, preferably 0.1 to 2wt.%.
8. the compositions according to aforementioned any one of claim, wherein said cationic polymer is Cationic polysaccharide polymer, it is preferable that cation guar gum and/or cationic cellulose polymer.
9. compositions according to claim 8, wherein said Cationic polysaccharide polymer is cationic cellulose polymer, it is preferable that quaternised hydroxyethyl cellulose.
11. the compositions according to aforementioned any one of claim, wherein said compositions comprises the composition selected from fatty acid or its salt, dope dye, enzyme, antiredeposition polymer, dye transfer inhibiting polymers, builder, chelating agen, opacifier, fluorescent agent, aromatic and/or soil release polymer further.
12. the compositions according to any one of claim 1 to 11 is for the purposes of softening fabrics.
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| Application Number | Priority Date | Filing Date | Title |
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| EP13194579 | 2013-11-27 | ||
| EP13194579.2 | 2013-11-27 | ||
| PCT/EP2014/074345 WO2015078692A1 (en) | 2013-11-27 | 2014-11-12 | Laundry compositions |
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| EP (1) | EP3074495B1 (en) |
| CN (1) | CN105745314B (en) |
| BR (1) | BR112016011675B1 (en) |
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| WO2018028928A1 (en) | 2016-08-10 | 2018-02-15 | Unilever Plc | Laundry composition |
| EP3497196B1 (en) | 2016-08-10 | 2020-01-29 | Unilever PLC | Laundry composition |
| WO2018060056A1 (en) * | 2016-09-29 | 2018-04-05 | Unilever Plc | Laundry composition |
| EP3519546B1 (en) * | 2016-09-29 | 2020-03-18 | Unilever PLC | Laundry composition |
| WO2018146256A1 (en) * | 2017-02-13 | 2018-08-16 | Unilever Plc | Use of a silicone in a laundry composition |
| CN110291179B (en) | 2017-02-13 | 2021-11-16 | 联合利华知识产权控股有限公司 | Laundry adjunct composition |
| CN110352232A (en) | 2017-02-13 | 2019-10-18 | 荷兰联合利华有限公司 | Laundry composition additive |
| EP3580318B1 (en) | 2017-02-13 | 2023-05-10 | Unilever IP Holdings B.V. | Method of delivering a laundry composition |
| MX2020005977A (en) * | 2017-12-06 | 2020-08-24 | Kao Corp | Soil release agent. |
| US11814607B2 (en) | 2018-03-02 | 2023-11-14 | Conopco, Inc. | Laundry additive composition comprising a soil release polymer/silicone mixture |
| WO2019166477A1 (en) * | 2018-03-02 | 2019-09-06 | Unilever Plc | Laundry composition |
| WO2019166476A1 (en) * | 2018-03-02 | 2019-09-06 | Unilever Plc | Laundry composition |
| EP3759206B1 (en) * | 2018-03-02 | 2024-04-03 | Unilever IP Holdings B.V. | Method of softening a laundry composition |
| US11939555B2 (en) | 2018-09-06 | 2024-03-26 | Dow Global Technologies Llc | Fabric care composition |
| WO2020091988A1 (en) | 2018-10-29 | 2020-05-07 | Dow Global Technologies Llc | Fabric care composition with silicone |
| WO2021118774A1 (en) * | 2019-12-13 | 2021-06-17 | Rohm And Haas Company | Fabric care composition |
| US11220657B2 (en) | 2019-12-31 | 2022-01-11 | Henkel IP & Holding GmbH | Solid perfume composition delivering softening |
| US11447722B2 (en) | 2020-01-30 | 2022-09-20 | Henkel Ag & Co. Kgaa | Detergent composition for textile softening and anti-redeposition |
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| CN1145025A (en) * | 1994-03-02 | 1997-03-12 | 花王株式会社 | Hair cosmetic composition |
| US20040103483A1 (en) * | 2002-11-04 | 2004-06-03 | The Procter & Gamble Company | Fabric treatment compositions comprising oppositely charged polymers |
| US20060030513A1 (en) * | 2004-08-03 | 2006-02-09 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Softening laundry detergent |
| CN101939406A (en) * | 2008-02-05 | 2011-01-05 | 株式会社资生堂 | Cleansing composition |
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| EP0070074B2 (en) | 1981-07-13 | 1997-06-25 | THE PROCTER & GAMBLE COMPANY | Foaming surfactant compositions |
| GB8803036D0 (en) | 1988-02-10 | 1988-03-09 | Unilever Plc | Liquid detergents |
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2014
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1145025A (en) * | 1994-03-02 | 1997-03-12 | 花王株式会社 | Hair cosmetic composition |
| US20040103483A1 (en) * | 2002-11-04 | 2004-06-03 | The Procter & Gamble Company | Fabric treatment compositions comprising oppositely charged polymers |
| US20060030513A1 (en) * | 2004-08-03 | 2006-02-09 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Softening laundry detergent |
| CN101939406A (en) * | 2008-02-05 | 2011-01-05 | 株式会社资生堂 | Cleansing composition |
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| BR112016011675B1 (en) | 2021-11-30 |
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| WO2015078692A1 (en) | 2015-06-04 |
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| CN105745314B (en) | 2018-09-14 |
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