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
  • C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/83—Mixtures of non-ionic with anionic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/02—Anionic compounds
  • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
  • C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
  • C11D1/143—Sulfonic acid esters
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/02—Anionic compounds
  • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
  • C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
  • C11D1/146—Sulfuric acid esters
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/72—Ethers of polyoxyalkylene glycols

Definitions

• the present invention relates to built laundry detergent compositions containing anionic sulphonate or sulphate surfactants and exhibiting increased mildness to the skin.
• Heavy duty laundry detergent compositions have for many years contained an anionic sulphonate or sulphate surfactant, for example, linear alkylbenzene sulphonate (LAS) or primary alcohol sulphate (PAS), as the principal detergent-active ingredient.
• anionic surfactants are frequently used in conjunction with ethoxylated alcohol nonionic surfactants which give improved detergency on hydrophobic soils.
• the nonionic surfactants generally have alkyl chain lengths of C 12 -C 18 and degrees of ethoxylation of 1 to 10.
• anionic and anionic/nonionic surfactant systems are robust and highly efficient on a wide range of soils and under a wide range of conditions, for example, temperature and water hardness. However, they are not noted for mildness to skin. These materials are designed to interact with fatty materials like body soil and protein residues on soiled laundry, and can therefore interact with the skin to give reactions such as dryness and erythema (redness).
• the milder surfactants used to formulate products intended for prolonged skin contact, for example, shampoos and shower gels would not perform adequately in heavy duty laundry detergent compositions because of insufficient interaction with fatty materials occurring as soil.
• Alkylpolyglycosides have been widely disclosed in the art as environmentally friendly carbohydrate-derived nonionic surfactants, and are used in various detergent and personal care products. Disclosures in the prior art include EP 75 994A, EP 75 995A and EP 75 996A (Procter & Gamble), EP 238 638B (Staley/Henkel), EP 487 262A (Unilever), EP 495 176 (Huels), EP 374 702A (Kao), WO 92 06150 (P&G), WO 94 26861A (Henkel), WO 94 24242 (P&G) and WO 96 29977 (Henkel). The use of APGs as detergency builders has been disclosed in EP 976 817A (Henkel).
• WO 00 08129A discloses mild particulate laundry detergent compositions based on high-foaming anionic surfactant (for example linear alkylbenzene sulphonate) plus one or more milder cosurfactants, for example, amine oxide or cocoamidopropyl betaine.
• high-foaming anionic surfactant for example linear alkylbenzene sulphonate
• milder cosurfactants for example, amine oxide or cocoamidopropyl betaine.
• the present invention provides the use of a an alkylpolyglycoside in an amount of from 0.5 to 5 wt% to increase the mildness to skin of a built particulate laundry detergent composition containing an anionic sulphonate or sulphate detergent.
• the invention is based on the observation that use of alkylpolyglycoside (APG) at low levels to replace part of a conventional anionic/nonionic surfactant system results in a measurable increase in mildness to skin.
• APG alkylpolyglycoside
• the built particulate laundry detergent composition contains:
• Preferred detergent compositions utilising the invention contain a conventional anionic sulphonate or sulphate surfactant and a conventional nonionic surfactant, and also contain as an essential ingredient a low level of alkylpolyglycoside.
• the built particulate laundry detergent composition comprises:
• the skin-mild detergent compositions of the invention are free of enzymes, since enzymes can also cause skin irritation to sensitive individuals.
• enzymatic compositions are also within the scope of the invention.
• anionic sulphonate or sulphate surfactant (i)
• Anionic sulphonate and sulphate surfactants are well-known to those skilled in the art. Many suitable detergent-active compounds are available and are fully described in the literature, for example, in "Surface-Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
• alkylbenzene sulphonates examples include alkylbenzene sulphonates, primary and secondary alkylsulphates, particularly C 8 -C 15 primary alkyl sulphates; alkyl ether sulphates; olefin sulphonates; alkyl xylene sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
• Sodium salts are generally preferred.
• the anionic surfactant is linear alkylbenzene sulphonate or primary alcohol sulphate. More preferably the anionic surfactant is linear alkylbenzene sulphonate.
• Conventional nonionic detergent surfactants are ethoxylated alcohols of the formula R 1 - (- O - CH 2 - CH 2 ) m - OH wherein R 1 is a C 8 -C 20 hydrocarbyl chain, and the average degree of ethoxylation m is generally from 1 to 10, preferably from 3 to 8.
• the alkyl chain length is preferably in the C 12 to C 15 range.
• Alkylpolyglycosides may be represented by the general formula I RO(R'O) t (G) x in which R is a hydrocarbyl group containing from 10 to 20 carbon atoms, R' is an alkylene group containing from 2 to 4 carbon atoms, G is a saccharide residue containing 5 or 6 carbon atoms, t is in the range of from 0 to 25 and x is in the range of from 1 to 10.
• the hydrophobic group R may be aliphatic, either saturated or unsaturated, notably linear or branched alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl. However, it may include an aryl group for example alkyl-aryl, alkenyl-aryl and hydroxyalkyl-aryl.
• the preferred R group is an alkyl or alkenyl group having from 8 to 20 carbon atoms, more preferably from 8 to 16 carbon atoms.
• the most preferred R group is an alkyl group having from 12 to 14 carbon atoms.
• t in the general formula above is preferably zero, so that the -(RO) t - unit of the general formula is absent. In that case the general formula becomes RO(G) x
• R'O is an ethylene oxide residue.
• Other likely possibilities are propylene oxide and glycerol residues.
• the value of t (which may be an average value) will preferably lie in the range of from 0.5 to 10.
• the group G is typically derived from fructose, glucose, mannose, galactose, talose, gulose, allose, altrose, idose, arabinose, xylose, lyxose and/or ribose.
• the group G is provided substantially exclusively by glucose units.
• x which is an average, is usually termed the degree of polymerisation (dp). Desirably x is within the range of from 1 to 8. Preferred values of x lie within the range of from 1 to 3, especially from 1 to 1.8 and more especially from 1 to 1.6.
• R is C 8 to C 14 alkyl or alkenyl.
• R is C 8 to C 14 alkyl or alkenyl
• t is zero
• x is within the range of from 1 to 1.6.
• Most preferably R is C 12 -C 14
• t is zero
• x is 1.4.
• Commercially available products suitable for use in the compositions of the invention include the Plantacare (Trade Mark) and Glucopon (Trade Mark) ranges ex Cognis Germany; Lutensol (Trade Mark) GD 70 ex BASF; Marlosan (Trade Mark) 24 ex Hüls; and Atlas (Trade Mark) G73500 ex ICI.
• compositions of the invention also contain from 10 to 80%, preferably from 15 to 70% by weight, of detergency builder.
• the quantity of builder is in the range of from 15 to 50% by weight.
• the builder is selected from zeolite, sodium tripolyphosphate, sodium carbonate, sodium citrate, layered silicate, and combinations of these.
• the zeolite used as a builder may be the commercially available zeolite A (zeolite 4A) now widely used in laundry detergent powders.
• the zeolite may be maximum aluminium zeolite P (zeolite MAP) as described and claimed in EP 384 070B (Unilever), and commercially available as Doucil (Trade Mark) A24 from Ineos Silicas Ltd, UK.
• Zeolite MAP is defined as an alkali metal aluminosilicate of zeolite P type having a silicon to aluminium ratio not exceeding 1.33, preferably within the range of from 0.90 to 1.33, preferably within the range of from 0.90 to 1.20. Especially preferred is zeolite MAP having a silicon to aluminium ratio not exceeding 1.07, more preferably about 1.00.
• the particle size of the zeolite is not critical. Zeolite A or zeolite MAP of any suitable particle size may be used.
• phosphate builders especially sodium tripolyphosphate.
• This may be used in combination with sodium orthophosphate, and/or sodium pyrophosphate.
• inorganic builders that may be present additionally or alternatively include sodium carbonate, layered silicate, amorphous aluminosilicates.
• Organic builders that may be present include polycarboxylate polymers such as polyacrylates and acrylic/maleic copolymers; polyaspartates; monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-di- and trisuccinates, carboxymethyloxysuccinates, carboxy-methyloxymalonates, dipicolinates, hydroxyethyliminodiacetates, alkyl- and alkenylmalonates and succinates; and sulphonated fatty acid salts.
• polycarboxylate polymers such as polyacrylates and acrylic/maleic copolymers
• polyaspartates monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-di- and trisuccinates, carboxymethyloxysuccinates, carboxy-methyloxymalonates, dipicolinates, hydroxyethyliminodiacetates, alky
• Organic builders may be used in minor amounts as supplements to inorganic builders such as phosphates and zeolites.
• Especially preferred supplementary organic builders are citrates, suitably used in amounts of from 5 to 30 wt %, preferably from 10 to 25 wt %; and acrylic polymers, more especially acrylic/maleic copolymers, suitably used in amounts of from 0.5 to 15 wt %, preferably from 1 to 10 wt%.
• Builders, both inorganic and organic are preferably present in alkali metal salt, especially sodium salt, form.
• compositions may optionally contain bleaching components and other active ingredients to enhance performance and properties.
• optional ingredients may include, but are not limited to, any one or more of the following: soap, peroxyacid and persalt bleaches, bleach activators, sequestrants, cellulose ethers and esters, other antiredeposition agents, sodium sulphate, sodium silicate, sodium chloride, calcium chloride, sodium bicarbonate, other inorganic salts, proteases, lipases, cellulases, amylases, other detergent enzymes, fluorescers, photobleaches, polyvinyl pyrrolidone, other dye transfer inhibiting polymers, foam controllers, foam boosters, acrylic and acrylic/maleic polymers, citric acid, soil release polymers, fabric conditioning compounds, coloured speckles, and perfume.
• Detergent compositions according to the invention may suitably contain a bleach system.
• the bleach system is preferably based on peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, capable of yielding hydrogen peroxide in aqueous solution.
• Suitable peroxy bleach compounds include organic peroxides such as urea peroxide, and inorganic persalts such as the alkali metal perborates, percarbonates, perphosphates, persilicates and persulphates.
• Preferred inorganic persalts are sodium perborate monohydrate and tetrahydrate, and sodium percarbonate.
• sodium percarbonate having a protective coating against destabilisation by moisture Sodium percarbonate having a protective coating comprising sodium metaborate and sodium silicate is disclosed in GB 2 123 044B (Kao).
• the peroxy bleach compound is suitably present in an amount of from 5 to 35 wt%, preferably from 10 to 25 wt%.
• the peroxy bleach compound may be used in conjunction with a bleach activator (bleach precursor) to improve bleaching action at low wash temperatures.
• the bleach precursor is suitably present in an amount of from 1 to 8 wt%, preferably from 2 to 5 wt%.
• Preferred bleach precursors are peroxycarboxylic acid precursors, more especially peracetic acid precursors and peroxybenzoic acid precursors; and peroxycarbonic acid precursors.
• An especially preferred bleach precursor suitable for use in the present invention is N,N,N',N'-tetracetyl ethylenediamine (TAED).
• TAED N,N,N',N'-tetracetyl ethylenediamine
• peroxybenzoic acid precursors in particular, N,N,N-trimethylammonium toluoyloxy benzene sulphonate.
• a bleach stabiliser may also be present.
• Suitable bleach stabilisers include ethylenediamine tetraacetate (EDTA) and the polyphosphonates such as Dequest (Trade Mark), EDTMP.
• EDTA ethylenediamine tetraacetate
• Dequest Trade Mark
• EDTMP Dequest (Trade Mark)
• enzymes are preferably absent, in other embodiments detergent enzymes may be present.
• Suitable enzymes include the proteases, amylases, cellulases, oxidases, peroxidases and lipases usable for incorporation in detergent compositions.
• detergency enzymes are commonly employed in granular form in amounts of from about 0.1 to about 3.0 wt%. However, any suitable physical form of enzyme may be used in any effective amount.
• Antiredeposition agents for example cellulose esters and ethers, for example sodium carboxymethyl cellulose, may also be present.
• compositions may also contain soil release polymers, for example sulphonated and unsulphonated PET/POET polymers, both end-capped and non-end-capped, and polyethylene glycol/polyvinyl alcohol graft copolymers such as Sokolan (Trade Mark) HP22.
• soil release polymers for example sulphonated and unsulphonated PET/POET polymers, both end-capped and non-end-capped, and polyethylene glycol/polyvinyl alcohol graft copolymers such as Sokolan (Trade Mark) HP22.
• soil release polymers for example sulphonated and unsulphonated PET/POET polymers, both end-capped and non-end-capped, and polyethylene glycol/polyvinyl alcohol graft copolymers such as Sokolan (Trade Mark) HP22.
• soil release polymers for example sulphonated and unsulphonated PET/POET polymers, both end-capped and non-end-capped, and polyethylene glycol/polyviny
• Powders of low to moderate bulk density may be prepared by spray-drying a slurry, and optionally postdosing (dry-mixing) further ingredients.
• “Concentrated” or “compact” powders may be prepared by mixing and granulating processes, for example, using a high-speed mixer/granulator, or other non-tower processes.
• Tablets may be prepared by compacting powders, especially "concentrated” powders.
• Model formulation solutions were prepared containing the ingredients shown in the table below. The solutions were buffered to a pH of 10.5 which is typical for wash liquors. weight % Total surfactant 0, 0.7, 1.0 or 2.0 Zeolite MAP 0.18 Sodium carbonate 0.11 Sodium citrate 0.03 Water to 100%
• Example 3 Comparative Example F: laundry detergent powder formulations
• a typical wash liquor based on the formulation of Example 3 (prepared by dissolving 115 g of formulation in 14.5 litres of water) is significantly milder than one based on the formulation of Comparative Example F.

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• Chemical & Material Sciences (AREA)
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• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Wood Science & Technology (AREA)
• Organic Chemistry (AREA)
• Detergent Compositions (AREA)

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Citations (9)

• 2001
  • 2001-10-10 GB GBGB0124306.2A patent/GB0124306D0/en not_active Ceased
• 2002
  • 2002-09-11 AT AT02256296T patent/ATE314449T1/de not_active IP Right Cessation
  • 2002-09-11 DE DE60208290T patent/DE60208290T2/de not_active Expired - Lifetime
  • 2002-09-11 ES ES02256296T patent/ES2252397T3/es not_active Expired - Lifetime
  • 2002-09-11 EP EP02256296A patent/EP1302531B1/de not_active Revoked

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