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WO2012049033A1 - Procédé à cuve à laver le linge à chargement par le haut - Google Patents

Procédé à cuve à laver le linge à chargement par le haut Download PDF

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Publication number
WO2012049033A1
WO2012049033A1 PCT/EP2011/067159 EP2011067159W WO2012049033A1 WO 2012049033 A1 WO2012049033 A1 WO 2012049033A1 EP 2011067159 W EP2011067159 W EP 2011067159W WO 2012049033 A1 WO2012049033 A1 WO 2012049033A1
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WO
WIPO (PCT)
Prior art keywords
surfactant
process according
water
particle
detergent particle
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.)
Ceased
Application number
PCT/EP2011/067159
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English (en)
Inventor
Stephen Thomas Keningley
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.)
Hindustan Unilever Ltd
Unilever NV
Original Assignee
Hindustan Unilever Ltd
Unilever NV
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 Hindustan Unilever Ltd, Unilever NV filed Critical Hindustan Unilever Ltd
Priority to EP11763944.3A priority Critical patent/EP2627751B1/fr
Priority to BR112013009127-4A priority patent/BR112013009127B1/pt
Priority to CN201180049085.7A priority patent/CN103282477B/zh
Publication of WO2012049033A1 publication Critical patent/WO2012049033A1/fr
Priority to ZA2013/02655A priority patent/ZA201302655B/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/046—Salts
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/08—Silicates
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/10—Carbonates ; Bicarbonates

Definitions

  • the present invention relates to laundry cleaning methods using shaped laundry detergent particles.
  • compositions sold and used are provided as liquids and powders. Powders are a traditional format in many places and users value the effective cleaning that they provide. However, some negatives can be perceived due to the build-up of residues on articles being washed. In part, these residues are due to ash, other un-dissolved solids (for example zeolite builders) and/or due to precipitating builders. The eventual consequence of this build-up can be colour changes of articles which have been laundered.
  • Liquid detergents do not have these same residue problems, but as they are largely un-built systems, they can suffer cleaning disadvantages especially in hard-water areas. Liquids have other advantages over powders, for example they do not have the caking problems of solids.
  • W01999/32599 describes a method of manufacturing laundry detergent particles, by extrusion of a builder and surfactant to form noodles.
  • a composition with a major component of a sulphated or sulphonated anionic surfactant is fed into an extruder, mechanically worked at a temperature of at least 40 °C, preferably at least 60°C, and extruded through an extrusion head having a multiplicity of extrusion apertures.
  • the surfactant is fed to the extruder along with builder in a weight ratio of more than 1 part builder to 2 parts surfactant.
  • the extruded material apparently required further drying.
  • PAS paste was dried and extruded.
  • Such PAS noodles are well known in the prior art.
  • the noodles are typically cylindrical in shape and their length exceeds their diameter, as described in example 2.
  • EP application 09158717.0 discloses high active detergent particles with a low surface roughness produced by extrusion of an anionic surfactant rich composition, and cutting of the extruded product to form slices which are thinner than they are wide. These slices are then spray-coated with, for example, an aqueous solution of sodium carbonate, to form smooth-surfaced, free-flowing particles which may look like "lentils". It is stated in that specification that use of a builder salt such as sodium carbonate is advantageous because it buffers the pH at a level where the anionic surfactant is particularly effective, and increases the ionic strength. The particles are also said to dissolve well in water and are suitable for use in a front loading washing machine (page 6, line 19). Our related, also unpublished, EP application 09158718.8 discloses high active granules which comprise a major amount of linear alkyl benzene sulphonate.
  • coated extruded particles with a particular shape and formulation show exceptionally good cleaning and care as perceived by a panel of users.
  • the coating is formulated with sodium carbonate monohydrate the particles do not exhibit a "hot on hands" feeling when used.
  • the present invention provides a laundry process which comprises the steps of:
  • iii) from 0 to 20 wt% other ingredients, including less than 15wt% water insoluble materials including fragrance, and, wherein the inorganic salts are present on the laundry detergent particle as a coating and the surfactant is present as a core.
  • step (c) rinsing and drying said articles wherein at least step (c) is performed in a top-loading washing vessel.
  • the surfactant to builder ratio in the detergent particles is in the range 1 .5-2.5:1 , more preferably 1 .8-2.2: 1 .
  • the ratio shifts further towards high builder levels the wash liquor becomes too alkaline and as it shifts towards high surfactant levels buffering capacity is lost.
  • the builder present as a coating encasing the surfactant, which is soft and sticky, a particulate concentrate with the preferred ratio of surfactant to builder can be provided.
  • the absence of other materials (carriers for the surfactant, fillers etc) reduce the unit dose required for a wash and therefore reduces transportation costs and increases shelf-use efficiency. Environmental impact of chemicals is also reduced. Dosage will typically be significantly smaller than with conventional products, around 0.5-1 g/L of fully formulated product for top loading machines and 1 -3 g/L for hand-wash vessels.
  • the coated laundry detergent particle has a non-spherical surface. Preferably this surface is in part curved.
  • the coated laundry detergent particle may be described as disk-like, lenticular or an oblate spheroid/ellipsoid, where z and y are the equatorial diameters and x is the polar diameter. It is preferred that y and z are similar in value, although with some methods of manufacture they may differ slightly due to pressures exerted during slicing of an extruded product.
  • the particles have an axis of rotational symmetry along the polar axis.
  • the coated laundry detergent particle does not have any holes; that is to say, the coated laundry detergent particle has a topologic genus of zero.
  • y and z are independently in the range 3 to 8 mm. This moves the shape further from a sphere and increases the ratio of surface area to volume, improving solubility.
  • the thickness of coating obtainable by use of a particular coating level is significantly greater than would be achieved on typically sized detergent granules (0.5-2mm diameter sphere). This makes for a more robust coating and reduces the tendency of the surfactant to bleed through the coating and make the particles sticky. It is also the case that a significant proportion of the builder will dissolve before the surfactant starts to dissolve so that the wash liquor will be at least partially built before the surfactant is dissolved.
  • a further advantage of these relatively large particles in the top-loader is that they sink rapidly and come into contact with the impeller at an early stage in the wash.
  • this surface area to volume ratio must be greater than 3 mm "1 .
  • the coating thickness is inversely proportional to this coefficient and hence for the coating the ratio "Surface area of coated particle” divided by "Volume of coated particle” should be less than 15 mm "1 .
  • the coated laundry detergent particle is such that at least 90 to 100% of the coated laundry detergent particles in the in the average x, y and z
  • dimensions of individual particles are within a 20%, preferably 10%, variable from the largest to the smallest coated laundry detergent particle. These aggregations of particles with similar sizes show good flow properties, can be packaged in bottles and can be dosed like a liquid.
  • the detergent particles comprise from 0.0001 to 0.1 wt % dye, preferably 0.001 to 0.01 wt % dye, wherein the dye is selected: from anionic dyes; and, non-ionic dyes.
  • Dyes serve several useful functions. They may assist the user in recognising different products, and/or may act as shading agents to mask yellowness of articles being laundered. If is preferable that not all of the particles are of the same colour, and that two or more colours of particles are present, for example white and blue, white and pink or white and orange.
  • wt % refer to the total percentage in the particle as dry weights (including water of hydration where present).
  • a top loading washing vessel is any vessel which is used by end-users to launder clothes.
  • such vessels have a capacity in excess of 4 litres.
  • Such vessels include, and preferentially comprise, top loading semi-automatic and automatic washing machines, preferably with means to agitate the wash liquor within them, and, in addition or in the alternative, other vessels where the agitation is manual, preferably a bath, tub, bucket, basin, bowl or sink.
  • Machines include machines such as and similar to a Brazilian “Tanquinho".
  • the vessel is open at the top during the washing operation and at least part of the agitation is provided by hand.
  • the coated laundry detergent particle comprises between 50 to 90 wt% of a surfactant, most preferably 70 to 90 wt%.
  • a surfactant most preferably 70 to 90 wt%.
  • the nonionic and anionic surfactants of the surfactant system may be chosen from the surfactants described "Surface Active Agents" Vol. 1 , by Schwartz & Perry, Interscience 1949, Vol. 2 by Schwartz, Perry & Berch, Interscience 1958, in the current edition of "McCutcheon's Emulsifiers and Detergents” published by Manufacturing Confectioners Company or in "Tenside-Taschenbuch", H. Stache, 2nd Edn., Carl Hauser Verlag, 1981 .
  • the surfactants used are saturated.
  • Suitable anionic detergent compounds which may be used are usually water- soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
  • suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher Cs to Ci8 alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl Cg to C20 benzene sulphonates, particularly sodium linear secondary alkyl C10 to C15 benzene sulphonates; and sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum.
  • anionic surfactants are sodium lauryl ether sulfate (SLES), particularly preferred with 1 to 3 ethoxy groups, sodium do to C15 alkyl benzene sulphonates (LAS) and sodium C12 to C18 alkyl sulphates (PAS).
  • Alkyl ester suphonates such as Methyl ester sulphonates (MES) may be used in whole or part replacement for the other anionics.
  • surfactants such as those described in EP-A-328 177
  • the fatty acid soap used preferably contains from about 16 to about 22 carbon atoms, preferably in a straight chain configuration.
  • the anionic contribution from soap is preferably from 0 to 30 wt% of the total anionic.
  • At least 50 wt % of the anionic surfactant is selected from: sodium Cn to C-I 5 alkyl benzene sulphonates; and, sodium C12 to C18 alkyl sulphates. Even more preferably, the anionic surfactant is sodium Cn to C15 alkyl benzene sulphonates.
  • the anionic surfactant is present in the coated laundry detergent particle at levels between 15 to 85 wt%, more preferably 50 to 80wt% on total surfactant.
  • Nonionic Surfactants :
  • Suitable nonionic detergent compounds which may be used include, in particular, the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
  • Preferred nonionic detergent compounds are Ce to C22 alkyl phenol- ethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, and the condensation products of aliphatic Cs to C18 primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 50 EO.
  • the non-ionic is 10 to 50 EO, more preferably 20 to 35 EO.
  • Alkyl ethoxylates are particularly preferred, most particularly those with 25-35 EO, as these give a particularly good foam profile.
  • the nonionic surfactant is present in the coated laundry detergent particle at levels between 5 to 75 wt% on total surfactant, more preferably 10 to 40 wt% on total surfactant.
  • Cationic surfactant may be present as minor ingredients at levels preferably between 0 to 5 wt% on total surfactant.
  • surfactants are mixed together before being dried. Conventional mixing equipment may be used.
  • the surfactant core of the laundry detergent particle may be formed by extrusion or roller compaction and subsequently coated with an inorganic salt.
  • Foam boosters such as betaines, amine oxides and/or other zwitterionic and aphphoteric surfactants are optional as the compositions of the invention generally show adequate foaming.
  • Calcium Tolerant Surfactant System :
  • the surfactant system used is calcium tolerant and this is a preferred aspect because this reduces the need for builder.
  • Such blends are called calcium tolerant surfactant blends if they pass the test set out hereinafter.
  • the invention may also be of use for washing with soft water, either naturally occurring or made using a water softener. In this case, calcium tolerance is no longer important and blends other than calcium tolerant ones may be used. Calcium-tolerance of the surfactant blend is tested as follows:
  • the surfactant blend in question is prepared at a concentration of 0.7 g surfactant solids per litre of water containing sufficient calcium ions to give a French hardness of 40 (4 x 10 "3 Molar Ca 2+ ).
  • Other hardness ion free electrolytes such as sodium chloride, sodium sulphate, and sodium hydroxide are added to the solution to adjust the ionic strength to 0.05M and the pH to 10.
  • the adsorption of light of wavelength 540 nm through 4 mm of sample is measured 15 minutes after sample preparation. Ten measurements are made and an average value is calculated. Samples that give an absorption value of less than 0.08 are deemed to be calcium tolerant.
  • Suitable calcium tolerant co- surfactants include SLES 1 -7EO, and alkyl-ethoxylate nonionic surfactants, particularly those with melting points less than 40°C.
  • a LAS/SLES surfactant blend has a superior foam profile to a LAS nonionic surfactant blend and is therefore preferred for hand washing formulations requiring high levels of foam.
  • SLES may be used at levels of up to 30wt% of the surfactant blend.
  • the water-soluble inorganic salts are preferably selected from water soluble salts of carbonate, chloride, silicate and sulphate, or mixtures thereof, most preferably, 70 to 100 wt% sodium carbonate on total water-soluble inorganic salts.
  • the water-soluble inorganic salt is present as a coating on the particle.
  • the amount of coating should lay in the range 1 to 40 wt% of the particle, preferably 20 to 40 wt%, more preferably 25 to 35 wt% for the best results in terms of anti-caking properties of the detergent particles.
  • the coating is preferably applied to the surface of the surfactant core, by deposition from an aqueous solution of the water soluble inorganic salt.
  • aqueous solution preferably contains greater than 50g/L, more preferably 200 g/L of the salt.
  • An aqueous spray-on of the coating solution in a fluidised bed has been found to give good results and may also generate a slight rounding of the detergent particles during the fluidisation process. Drying and/or cooling may be needed to finish the process.
  • a preferred calcium tolerant coated laundry detergent particle comprises 15 to 100 wt% on surfactant of anionic surfactant of which 20 to 30 wt% on surfactant is sodium lauryl ether sulphate.
  • a highly preferred water soluble inorganic salt for inclusion in the coating is sodium carbonate monohydrate. Where, during the wash process, the coated detergent particles contact both water and the skin of the user, this confers the distinct benefit that upon exposure to water the particles do not generate as much heat as they would if the carbonate was anhydrous. This is an important preferred feature as users often mix detergent products with water by hand, and describe products which employ anhydrous sodium carbonate as having a "hot on hands" feeling.
  • the inorganic salts in the coating is 100% by weight sodium carbonate monohydrate. This gives the best protection against moisture.
  • the level of sodium carbonate monohydrate can be as low as 50% by weight of the inorganic salts in the coating.
  • Dyes are a highly preferred component of the present invention. Suitable dyes are described in Industrial Dyes edited by K.Hunger 2003 Wiley-VCH ISBN 3-527- 30426-6. Dyes for use in the current invention are selected from anionic and non-ionic dyes Anionic dyes are negatively charged in an aqueous medium at pH 7. Examples of anionic dyes are found in the classes of acid and direct dyes in the Color Index (Society of Dyers and Colourists and American Association of Textile Chemists and Colorists). Anionic dyes preferably contain at least one sulphonate or carboxylate groups. Non-ionic dyes are uncharged in an aqueous medium at pH 7, examples are found in the class of disperse dyes in the Color Index.
  • the dyes may be alkoxylated.
  • Alkoxylated dyes are preferably of the following generic form: Dye-NR-
  • R 2 group is attached to an aromatic ring of the dye.
  • Ri and R 2 are independently selected from polyoxyalkylene chains having 2 or more repeating units and preferably having 2 to 20 repeating units. Examples of polyoxyalkylene chains include ethylene oxide, propylene oxide, glycidol oxide, butylene oxide and mixtures thereof.
  • a preferred alkoxylated dye for use in the invention is:
  • the dye is selected from acid dyes; disperse dyes and alkoxylated dyes.
  • the dye is a non-ionic dye.
  • the dye is selected from those having: anthraquinone; mono-azo; bis- azo; xanthene; phthalocyanine; and, phenazine chromophores. More preferably the dye is selected from those having: anthraquinone and, mono-azo
  • the dye is added to the coating solution or slurry and agitated before applying to the core of the particle.
  • Application may be by any suitable method, preferably spraying on to the core particle as detailed above.
  • the dye may be any colour, preferable the dye is blue, violet, green or red. Most preferably the dye is blue or violet.
  • the dye is selected from: acid blue 80, acid blue 62, acid violet 43, acid green 25, direct blue 86, acid blue 59, acid blue 98, direct violet 9, direct violet 99, direct violet 35, direct violet 51 , acid violet 50, acid yellow 3, acid red 94, acid red 51 , acid red 95, acid red 92, acid red 98, acid red 87, acid yellow 73, acid red 50, acid violet 9, acid red 52, food black 1 , food black 2, acid red 163, acid black 1 , acid orange 24, acid yellow 23, acid yellow 40, acid yellow 1 1 , acid red 180, acid red 155, acid red 1 , acid red 33, acid red 41 , acid red 19, acid orange 10, acid red 27, acid red 26, acid orange 20, acid orange 6, sulphonated Al and Zn
  • phthalocyanines solvent violet 13, disperse violet 26, disperse violet 28, solvent green 3, solvent blue 63, disperse blue 56, disperse violet 27, solvent yellow 33, disperse blue 79: 1 .
  • the dye is preferably a shading dye for imparting a perception of whiteness to a laundry textile.
  • the dye may be covalently bound to polymeric species. A combination of dyes may be used.
  • the particle preferably comprises from 0 to 15 wt% water, more preferably 0 to 10 wt%, most preferably from 1 to 5 wt% water, at 293K and 50% relative humidity. This facilitates the storage stability of the particle and its mechanical properties.
  • Adjuncts The adjuncts as described below may be present in the coating or the core of the particle.
  • Fluorescent Agent The adjuncts as described below may be present in the coating or the core of the particle.
  • the coated laundry detergent particle preferably comprises a fluorescent agent (optical brightener).
  • fluorescent agents are well known and many such
  • fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts.
  • the total amount of the fluorescent agent or agents used in the composition is generally from 0.005 to 2 wt %, more preferably 0.01 to 0.1 wt %. Suitable fiuorescer for use in the invention are described in chapter 7 of Industrial Dyes edited by K. Hunger 2003 Wiley-VCH ISBN 3-527-30426-6.
  • Preferred fluorescers are selected from the classes of distyrylbiphenyls, triazinylaminostilbenes, bis(1 ,2,3-triazol-2-yl)stilbenes, bis(benzo[b]furan-2- yl)biphenyls, 1 ,3-diphenyl-2-pyrazolines and courmarins.
  • the fiuorescer is preferably sulfonated.
  • Preferred classes of fiuorescer 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.
  • Preferred fluorescers are: sodium 2 (4-styryl-3-sulfophenyl)- 2H-napthol[1 ,2-d]triazole, disodium 4,4'-bis ⁇ [(4-anilino-6-(N methyl-N-2
  • Tinopal® DMS is the disodium salt of disodium 4,4'-bis ⁇ [(4-anilino-6-morpholino- 1 ,3,5-triazin-2-yl)]amino ⁇ stilbene-2-2' disulfonate.
  • Tinopal® CBS is the disodium salt of disodium 4,4'-bis(2-sulfostyryl)biphenyl.
  • the composition comprises a perfume.
  • the perfume is preferably in the range from 0.001 to 3 wt%, most preferably 0.1 to 1 wt%.
  • CTFA Cosmetic, Toiletry and
  • perfume components there will be four or more, preferably five or more, more preferably six or more or even seven or more different perfume components.
  • perfume mixtures preferably 15 to 25 wt% are top notes. Top notes are defined by Poucher (Journal of the Society of Cosmetic Chemists 6(2):80 [1955]).
  • top-notes are selected from citrus oils, linalool, linalyl acetate, lavender, dihydromyrcenol, rose oxide and cis-3-hexanol.
  • the composition may comprise one or more polymers. Examples are:
  • carboxymethylcellulose poly (ethylene glycol), polyvinyl alcohol), polyethylene imines, ethoxylated polyethylene imines, water soluble polyester polymers polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacry late/acrylic acid copolymers.
  • One or more enzymes are preferred present in a composition of the invention.
  • the level of each enzyme is from 0.0001 wt% to 0.5 wt% protein on product.
  • enzymes include proteases, alpha-amylases, cellulases, lipases, peroxidases/oxidases, pectate lyases, and mannanases, or mixtures thereof.
  • 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 (7.
  • 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
  • lipase variants such as those described in WO 92/05249, WO 94/01541 , EP 407 225, EP 260 105, WO 95/35381 , WO 96/00292, WO 95/30744, WO 94/25578, WO 95/14783, WO 95/22615, WO 97/04079 and WO 97/07202, WO 00/60063, WO 09/107091 and WO09/1 1 1258.
  • LipolaseTM and Lipolase UltraTM LipexTM (Novozymes A/S) and LipocleanTM.
  • 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 classified as EC 3.1.1 .4 and/or EC 3.1 .1 .32 As used herein, the term
  • 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. Several types of phospholipase activity can be distinguished, including phospholipases Ai and A 2 which hydrolyze one fatty acyl group (in the sn-1 and sn-2 position, respectively) to form
  • lysophospholipid lysophospholipid
  • lysophospholipase or phospholipase B which can hydrolyze the remaining fatty acyl group in lysophospholipid.
  • Phospholipase C and phospholipase D release diacyl glycerol or
  • proteases include those of animal, vegetable or microbial origin. Microbial origin is preferred. Chemically modified or protein engineered mutants are included.
  • the protease may be a serine protease or a metallo protease, preferably an alkaline microbial protease or a trypsin-like protease.
  • Preferred commercially available protease enzymes include AlcalaseTM, SavinaseTM, PrimaseTM, DuralaseTM, DyrazymTM, EsperaseTM, EverlaseTM, PolarzymeTM, and KannaseTM, (Novozymes A/S), MaxataseTM, MaxacalTM, MaxapemTM,
  • the method of the invention may be carried out in the presence of cutinase.
  • cutinase used according to the invention may be of any origin.
  • cutinases are of microbial origin, in particular of bacterial, of fungal or of yeast origin.
  • 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. licheniformis, described in more detail in GB 1 ,296,839, or the Bacillus sp. strains disclosed in WO 95/026397 or WO 00/060060. Commercially available amylases are DuramylTM, TermamylTM, Termamyl UltraTM, NatalaseTM,
  • 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, EndolaseTM, RenozymeTM (Novozymes A/S), ClazinaseTM and Puradax HATM (Genencor International Inc.), and KAC-500(B)TM (Kao Corporation).
  • Suitable peroxidases/oxidases include those of plant, bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Examples of useful peroxidases 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). Further enzymes suitable for use are disclosed in WO2009/087524,
  • Enzyme Stabilizers are particularly preferred. It is particularly preferred to use a combination of lipase, protease and one or both of amylase and mannanase. Enzyme Stabilizers:
  • 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
  • Sequesterants e.g., WO 92/19709 and WO 92/19708.
  • Sequesterants for ions other than calcium and magnesium may be present in the coated laundry detergent particles.
  • Citrate is preferably present at a level of 5-15%wt on total particle. Citrate can be present either as the salt, or as the acid. When present as the acid evolved gas is generated on exposure of the particles to water. This can generate local turbulence which promotes dissolution and acts as a cue for cleaning.
  • Phosphonates, for example such as DequestTM 2010 can also be used as sequestering agents.
  • the coated laundry detergent particle does not contain a peroxygen bleach, e.g., percarbonate, perborate, and other peracids.
  • a peroxygen bleach e.g., percarbonate, perborate, and other peracids.
  • Preferred "chassis” formulations comprise:
  • Either of the LAS/NI based or LAS/PAS/SLES based options can be combined with citrate/citric acid at a level of 5-10 wt%.
  • Either formulation may comprise a soil release polymer, preferably a polyester material, for example Texcare SRN170 at a level of 1 -5 wt%.
  • the extruded product was cut after the die-plate using a high speed cutter set up to produce particle with a thickness of ⁇ 1.1 mm.
  • the cutter deforms the discs cut from the extruded product to give a slight difference between dimensions y and z.
  • the coating solution was fed to the spray nozzle of the Strea 1 via a peristaltic pump (Watson-Marlow model 101 U/R) at an initial rate of 3.3g/min, rising to 9.1 g/min during the course of the coating trial.
  • a peristaltic pump Wood-Marlow model 101 U/R
  • the Fluid bed coater was operated with an initial air inlet air temperature of 55°C increasing to 90°C during the course of the coating trial whilst maintaining the outlet temperature in the range 45-50°C throughout the coating process.
  • compositions of the present invention show significant improvement over the standard and while they are pourable composition they are also significantly better performing than conventional liquids.
  • SkipTM powder (ex Argentina) and the composition of the present invention was sewn into a black cotton cloth sachet. Washes were performed using the cycles mentioned in the table below. Before preparing the sachets the black cotton was prewashed 3 times at 60°C to prevent dye transfer during the black sachet test (Miele professional 350 g Robijn, 8 kg black cotton). Sachets were filled with 10 gram of the different detergent products. Results are shown below.
  • the temperature rise on dissolution of a composition of the present invention was compared with the temperature rise of commercial laundry compositions in both a tub formed from a plastics material and a glass jar. In both cases 75g of product was added to 70g of water. The temperature rise was monitored at intervals for 300 seconds. In all cases the temperature rise using the particles of the present invention was significantly less than that using the commercial products.
  • the results given below are temperatures for products as listed on the left, used with the tub.

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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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

L'invention concerne un procédé de lavage du linge qui comprend les étapes consistant à : a) se procurer des particules de détergent enrobées ayant des dimensions perpendiculaires x, y et z, où x est de 1 mm à moins de 2 mm, y est de plus de 2 mm à 8 mm et z est de plus de 2 mm à 8 mm, les particules comprenant : (i) de 50 à 90 % en poids d'agent tensio-actif choisi parmi un agent tensio-actif anionique et/ou un agent tensio-actif non ionique; (ii) de 1 à 40 % en poids de sels inorganiques solubles dans l'eau; (iii) de 0 à 20 % en poids d'autres ingrédients, comprenant moins de 15 % en poids de matières insolubles dans l'eau comprenant un parfum, les sels inorganiques étant présents sur les particules de détergent à lessive en tant qu'enrobage et l'agent tensio-actif étant présent en tant que noyau; b) dissoudre lesdites particules de détergent enrobées dans de l'eau pour former un bain de lavage; c) traiter des articles par ledit bain de lavage; d) séparer lesdits articles dudit bain de lavage, et e) rincer et sécher lesdits articles, au moins l'étape (c) étant réalisée dans une cuve de lavage à chargement par le haut.
PCT/EP2011/067159 2010-10-14 2011-09-30 Procédé à cuve à laver le linge à chargement par le haut Ceased WO2012049033A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP11763944.3A EP2627751B1 (fr) 2010-10-14 2011-09-30 Procédé à cuve à laver le linge à chargement par le haut
BR112013009127-4A BR112013009127B1 (pt) 2010-10-14 2011-09-30 Processo de lavagem de roupa
CN201180049085.7A CN103282477B (zh) 2010-10-14 2011-09-30 顶部装载洗衣容器的方法
ZA2013/02655A ZA201302655B (en) 2010-10-14 2013-04-12 Top-loading laundry vessel method

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP10187500.3 2010-10-14
EP10187500 2010-10-14

Publications (1)

Publication Number Publication Date
WO2012049033A1 true WO2012049033A1 (fr) 2012-04-19

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EP (1) EP2627751B1 (fr)
CN (1) CN103282477B (fr)
BR (1) BR112013009127B1 (fr)
WO (1) WO2012049033A1 (fr)
ZA (1) ZA201302655B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020109227A1 (fr) 2018-11-28 2020-06-04 Unilever N.V. Grosses particules

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020109227A1 (fr) 2018-11-28 2020-06-04 Unilever N.V. Grosses particules

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BR112013009127A2 (pt) 2016-07-19
EP2627751B1 (fr) 2015-06-03
CN103282477A (zh) 2013-09-04
ZA201302655B (en) 2014-06-25
EP2627751A1 (fr) 2013-08-21
BR112013009127B1 (pt) 2020-05-26
CN103282477B (zh) 2015-04-01

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