EP1237997A1 - Elastische formteile und deren anwendung - Google Patents

Elastische formteile und deren anwendung

Info

Publication number
EP1237997A1
EP1237997A1 EP00967305A EP00967305A EP1237997A1 EP 1237997 A1 EP1237997 A1 EP 1237997A1 EP 00967305 A EP00967305 A EP 00967305A EP 00967305 A EP00967305 A EP 00967305A EP 1237997 A1 EP1237997 A1 EP 1237997A1
Authority
EP
European Patent Office
Prior art keywords
article
water
matrix
elastic
mixture
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.)
Withdrawn
Application number
EP00967305A
Other languages
English (en)
French (fr)
Inventor
Matthew Grady Mcgoff
Hossam The Chimes Lodge TANTAWY
Christopher Charles Driffield
Scott Edward Stephens
Andrew Edward Bayly
Didier Marcel Corrand
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.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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
Priority claimed from GB9923344A external-priority patent/GB2355014A/en
Priority claimed from GB9923393A external-priority patent/GB2355008A/en
Priority claimed from GB0010599A external-priority patent/GB2361928A/en
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of EP1237997A1 publication Critical patent/EP1237997A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0208—Tissues; Wipes; Patches
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/10—Washing or bathing preparations
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34—Auxiliary operations
    • B29C44/3461—Making or treating expandable particles
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/30—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by mixing gases into liquid compositions or plastisols, e.g. frothing with air
    • 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
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0094—High foaming compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • 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
    • 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
    • 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
    • C11D3/3776—Heterocyclic compounds, e.g. lactam
    • 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
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38672—Granulated or coated enzymes
    • 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
    • C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/40—Specific cleaning or washing processes
    • C11D2111/42—Application of foam or a temporary coating on the surface to be cleaned

Definitions

  • the present invention relates to elastic articles, typically beads, particles or tablets, comprising a matrix of a polymeric material, a plasticiser and/ or water and an active ingredient, such as detergent ingredients, typically to be delivered to an aqueous environment.
  • the invention also relates to compositions containing the elastic articles and methods for making the elastic articles.
  • compositions such as cleaning products and personal-care products, cosmetics and pharmaceuticals, often comprise active ingredients which are to be delivered to water or which are required to be active in aqueous conditions, but which are sensitive to moisture, temperature changes, light and/or air during storage.
  • these compositions often contain ingredients which may react with one another. Therefore, such ingredient or actives are often protected or separated from one another by coating agents or encapsulating agents.
  • coating agents For example enzymes, used in detergents, are often incompatible with alkaline or acid materials, bleaches, moisture and light and thus coated to protect them. Because the active materials generally need to be delivered in aqueous conditions, the coating materials need to be chosen such that the coating and actives dissolve or disperse well in water.
  • the resulting elastic articles have been found to be very impact resistant, thus resulting in reduced braking-up or abrasion during handling and reduced dust formation.
  • elastic particles or beads with enzymes can thus be obtained which are safer and more efficient to handle.
  • these articles can be made such that they still deliver the actives very efficiently to liquid, e.g.aqueous, environments.
  • the article is in the form of a foam article, which is air-stable under normal humidity storage conditions, but unstable upon contact with water, to thus deliver the actives.
  • the elastic article is useful in any product, in particular useful in cleaning products, pharmaceutical products, personal-care products, cosmetic products and fabric-care products.
  • the invention relates to an elastic article comprising a) an active ingredient; b) a matrix formed from a polymeric material and a plasticiser, provided that when the plasticiser consist of water, the level of water is at least 3% by weight of the article (based on free-moisture level), whereby the article is capable of delivering the active to a liquid environment, and whereby the matrix has a glass transition temperature (Tg) below 50°C, preferably below 40°C, and whereby the active ingredient may be present in the matrix, or may be outside the matrix.
  • Tg glass transition temperature
  • the matrix has a Tg of less than 20°C or even from -20°C or even -10°C to 10°C or even to 0°C, and preferably the matrix has such an elasticity that it has an elastic modulus of less than IGN.m "2 , preferably less than 0.5 or even O. lGNm "2 .
  • the active ingredient is present in the matrix, for example that the polymer material and active ingredient are homogeneously mixed within the matrix, or for example, it may be preferred that the matrix is in the form of a coating or layer around the active ingredient.
  • the elastic article preferably releases the active ingredient or part thereof upon contact with water, the article and the matrix preferably partially or completely disintegrating, dispersing, denaturing and/ or dissolving upon contact with water.
  • the elastic article is preferable an elastic foam article.
  • the elastic article may preferably be in the form of particles or beads.
  • the active ingredients are cleaning actives, personal-care or cosmetic actives or pharmaceutical actives.
  • the elastic article may also contain mixtures of active ingredients, which may be particularly useful to improve the storing of active ingredients which can react with one another. By use of the elastic article, it can be achieved that such ingredients only become active once released into the aqueous conditions.
  • the article may comprise full compositions, or only some or one active ingredients to be incorporated in such compositions.
  • the invention also relates to processes for making the elastic article, and compositions comprising the elastic article.
  • the invention also relates to the use of elastic articles according to the invention to deliver active ingredients to an aqueous environment, preferably the active ingredients being detergent active ingredients and the aqueous environment being the wash water.
  • the elastic article can be such that delayed release of the active ingredient to the aqueous environment can be achieved.
  • the invention also relates to the use of an elastic article according to the invention to incorporate enzymes in compositions, preferably detergent compositions
  • the elastic article of the invention comprises a matrix comprising, and formed from, a polymeric material and a plasticiser and optionally other materials
  • the matrix may comp ⁇ se the active ingredient, or part thereof, or the active ingredient may be present outside the matrix, for example enclosed by the matrix (the matrix coating or encapsulating the active ingredient)
  • the polymer material and the active ingredient may be intimately mixed or even homogeneously mixed, in which case a so-called monophase elastic article is obtained, which has uniform physical and chemical properties
  • it may be preferred that the active ingredient and the polymeric material are present in the matrix in a non-homogeneous form, forming a multiphase elastic article, whereby on a microstructure level one or more of the active ingredients is present in lower or higher amounts in one area of the matrix than in an other area of the component, and thus lower or higher than the average obtained by intimate mixing
  • the active ingredient is piesent in the core or an inner shell oi layer of the article, enclosed by the matrix It may also be piefe ⁇ ed that part of the matrix forms a core or inner shell oi layer of the article, which is then enclosed by a layer of the active ingredient and then preferably by another layer of the matrix material
  • the elastic article comprises preferably at least 1% by weight of the active ingredients, more preferably from 5% to 70%, more preferably at least 10% by weight of the matrix, more preferably from 15% or even 20% or even 25% to 50%
  • the elastic article comprises preferably from 10% to 99% by weight of the matrix, more preferably at least 20% or even 30% to 99%, more preferably from 20% or 30% to 90% to 80% by weight
  • the plasticiser may consist of water, provided that it is then present at a level of at least 3% by weight of the article (based on free-moisture level).
  • at least a plasticiser other than water is present, as described below in more detail.
  • the matrix has a glass transition temperature Tg, as defined below, of less than 50°C, preferably less than 40°C preferably less than 20°C or even less than 10°C or even less than 0°C.
  • Tg glass transition temperature
  • the glass transition temperature is above -20°C or even above -10°C.
  • the Tg of the matrix when used herein is the Tg of the polymeric matrix as present in the article, which thus may be a mixture of polymeric material and plasticiser alone, or a mixture of polymeric material, plasticiser and active ingredient, and in either case, optional additional ingredients may be present (such as stabilisers, densification aids, fillers, lubricants etc., as described herein).
  • the glass transition temperature as used herein is as defined text book 'Dynamic Mechanical Analysis' (page 53, figure 3.11c on page 57), being the temperature of a material (matrix) where the material (matrix) changes from glassy to rubbery, namely where chains gain enough mobility to slide by each other.
  • the Tg of the matrix of the article of the invention can be measured in the Perkin-Elmer DMA 7e equipment, following the directions in operations manual for this equipment, generating a curve as illustrated in the book Dynamic Mechanical Analysis - page 57, figure 3-1 lc.
  • the Tg is the temperature or log Frequency as measured with this equipment, between the glass and 'leathery region', as defined in that text.
  • the matrix and preferably the elastic article as a whole, has a specific elasticity and flexibility, because of its specific glass transition temperature.
  • the elasticity can be defined by the elastic modulus of the matrix, or even the article, which again can be defined by the Young's modulus.
  • This can be calculated from strain or stress mechanical tests as known in the art, for example by using Perkin-Elmer DMA 7e equipment following the manufacturer's experimental procedure over a specific % static strain range, namely in the range of 10-40% static strain. This represents a maximum strain as could be applicable during normal manufactering or handling.
  • the elastic modulus as defined herein is the maximum modulus as measured with this equipment in the range of 10% to 40% static strain. For example a piece of matrix (or article) of 1 cm 3 can be used in the testing with this equipment.
  • the matrix herein typically has an elastic modulus or Young's modulus of less than 4 GN.m “2 , or typically less than 2 GN.m “2 , even more preferentially less than 1 GN.m “2 , but typically even less than 0.5 GN.m “ 2, or even less than 0.1 GN.m “ 2, or even less than 0.01 GN.m “2 , as measured with the Perkin-Elmer DMA 7e equipment.
  • a matrix herein which contains gas bubbles, e.g. formed by processes involving the introduction of air in the matrix has an elastic modulus below 0.1 GN.m “2 or even 0.01 GN.m “2 or even below 0.005 GN.m “2 or even below 0.0001 GN.m “2 .
  • the matrix is flexible, such that it has a relative yield strain greater than 2%, and preferably greater than 15% or even greater than 50%, as measured with the Perkin- Elmer DMA 7e equipment. (The yield strain is in this measurement the limit deformation of a piece of matrix at which the it deforms irreversible).
  • This can for example be measured by use of Perkin-Elmer DMA 7e equipment.
  • the matrix is preferably flexible to such an extend that when a matrix sample having a cross section of a specific length, for example 1cm, is stretched with a static force applied along the axis of that cross section, the static force being variable, but at least equivalent to twice atmospheric pressure, the change of this length after removal of the force is at least 90%) to 110% of the original length.
  • a matrix sample having a cross section of a specific length for example 1cm
  • the static force being variable, but at least equivalent to twice atmospheric pressure
  • this length of the cross section after this experiment is preferably from 90%) to 110%> of the original length of the cross section, preferably from 95%> to 105% or even from 98% to 100%.
  • the elastic modulus or Young's modulus is related to the relative density, namely
  • the elastic article of he invention is typically used to deliver actives to aqueous environment. Then, the elastic article, and preferably the matrix thereof, is unstable when brought into contact with water. This occurs such that the active ingredients or part thereof, present in the article is delivered to the water. Preferably the article or part thereof denatures, disintegrates, preferably disperses or dissolves in water.
  • the active ingredient is delivered rapidly and that the elastic article is such that the polymeric material of the matrix of the article disperses or dissolves rapidly; preferably at least 10%> of the polymeric material, by weight, is dissolved or dispersed in 30 minutes after contacting the article with water, or more preferably at least 30% or even at least 50% or even at least 70% or even at least 90% (introduced in the water at a 1% by weight concentration). It may even be preferred that this happens within 20 minutes or even 10 minutes or even 5 minutes after contacting the elastic article with the water.
  • the dissolution or dispersion can be measured by the method described herein after for measuring the dissolution and dispersion of polymers.
  • the elastic article is such that the total volume of the article is changed, preferably reduced, with at least 10%>, compared to the initial total volume, as for example can be determined when 1 cm 3 of the article is added to 100 ml of demineralised water upon and stirred for 5 minutes at a speed of 200rpm, at a temperature of 25°C.
  • the change, or preferably reduction, in total volume is at least 20% or even at least 40%) or even at least 60%> or even at least 90%> or even about 100%, e.g. because it may be preferred that substantially the whole article is disintegrated, dispersed or preferably dissolved into the water quickly.
  • Acetone is for example used when found to be neither denaturing and/or not interacting with the polymeric material in the matrix of the elastic article herein, for example when this is PVA.
  • Other neutral organic medium can be used according to the nature of the article under investigation; the inert solvent is such that the article is substantially not dissolved, dispersed, disintegrated or denatured by the solvent.
  • the cylinder is air sealed and left to rest for 1 minute so that the solvent penetrates the whole elastic article.
  • the change in volume is measured and taken as the original volume V, of the foam specimen.
  • the article is then removed from the solvent and left to dry in air so that the solvent evaporates.
  • the article is then placed in a 250 ml beaker containing 100 ml of demineralised water, maintained at 25°C, under stirring at 200 rpm with the help of a magnetic stirrer, for 5 minutes.
  • the remaining of the article specimen, if any, is filtered off with a 60mm mesh copper filter and placed in an oven at a temperature and for a period such that residual water is removed.
  • the dried remaining article is re-introduced in the measuring cylinder which volume of acetone had been re-adjusted to 50 ml.
  • the matrix of the elastic article has preferably a relative density p of from 0.01 to 0.95, more preferably from 0.05 to 0.9 or even from 0.1 to 0.8 or even form 0.3 to 0.7.
  • the relative density is the ratio of the density of the matrix or the article (p ), to the sum of the partial densities of all the bulk materials used to form the matrix, or the article (p s ).
  • the matrix or even the article as a whole is preferably in the form of a foam and preferably such that it forms an interconnected network of open and or closed cells, in particular a network of solid struts or plates which form the edges and faces of open and/ or closed cells.
  • the spacing inside the cells can contain part of the active ingredient and/ or a gas, such as air.
  • the ratio of the closed cells to open cells in the matrix of the article, or the article as a whole is more than 1 : 1, preferably more than 3:2 or even more than 2: 1 or even more than 3: 1.
  • the preferred foamed article or foamed matrix is typically air-stable or stable upon contact with air, which means herein that the bulk volume of the article or matrix thereof substantially remains the same when exposed to air.
  • the elastic article or the matrix thereof retains from 75%o to 125% or even from 90%> to 110% or even from 95%> to 100% of its bulk volume under the above storage conditions whereby the humidity is 80%).
  • the bulk volume change can be measured by any conventional method.
  • a digital image recorder system containing a digital camera coupled to a personal computer itself equipped with calibrated image analyser software.
  • a 1cm specimen of the article or the matrix thereof is obtained and introduced in an open beaker having a diameter of 9 cm and stored for 24 hours at the above conditions. After 24 hours, the size in all three dimensions is measured with the image analysis recorder system. Each specimen measurement is repeated three times, and the average bulk volume change is calculated in %>.
  • the elastic article or matrix thereof is such that, when in the form of particles of a mean particle size of 2000 microns or less, these particles also retain from 75% to 125% or even from 90% to 110% or even from 95% to 100% of their bulk volume.
  • This can for example be measured by placing 20 grams of such particles, or a weight comprising more than 500 particles, in a volumetric beaker having a diameter of 9 cm.
  • the beaker is taped lightly on its base until the elastic particles re-arrange themselves in a stable position with a horizontal top surface. The volume is measured.
  • the open beaker with the elastic particles is then carefully placed in the incubator for 24 hours, set to the desired %>RH and temperature.
  • the bulk volume after the 24 hours is measured and the change of bulk volume is calculated in %.
  • Any polymeric material can be used to form the matrix herein, provided it has itself a Tg as defined above or more typically, it can be formed into a matrix of the Tg as defined above by using a suitable amount of plasticiser.
  • the polymer material comprises or consists of amorphous polymer(s).
  • the polymeric material may consist of a single type of homologous polymer or may be a mixture of polymers. Mixtures of polymers may in particular be beneficial to control the mechanical and/or dissolution properties of the elastic article, depending on the application thereof and the requirements thereof.
  • the polymeric material comprises a water-dispersible or more preferably a water-soluble polymer.
  • Preferred water-dispersable polymers herein have a dispersability of at least 50%, preferably at least 75% or even at least 95%, as measured by the method set out hereinafter using a glass-filter with a maximum pore size of 50 microns; more preferably the polymer herein is a water-soluble polymer which has a solubility of at least 50%>, preferably at least 75% or even at least 95%>, as measured by the method set out hereinafter using a glass-filter with a maximum pore size of 20 microns, namely:
  • Gravimetric method for determining water-solubility or water-dispersability of polymers 50 grams ⁇ 0.1 gram of polymer is added in a 400 ml beaker, whereof the weight has been determined, and 245ml ⁇ 1ml of distilled water is added. This is stirred vigorously on magnetic stirrer set at 600 rpm, for 30 minutes. Then, the water-polymer mixture is filtered through a folded qualitative sintered-glass filter with the pore sizes as defined above (max. 20 or 50 microns). The water is dried off from the collected filtrate by any conventional method, and the weight of the remaining polymer is determined (which is the dissolved or dispersed fraction). Then, the % solubility or dispersability can be calculated.
  • PVP and derivatives thereof
  • PEG and derivatives thereof
  • PVA and derivatives thereof
  • such polymers have a level of hydrolysis of at least 50%>, more preferably at least 70% or even from 85% to 95%.
  • the polymer can have any average molecular weight, preferably from about 1000 to 1,000,000, or even form 4000 to 250,000 or even form 10,000 to 200,000 or even form 20,000 to 75,000. Highly preferred may be polymeric material having a weight average molecular weight of from 30,000 to 70,000.
  • Cross-linking agents may be added to modify the properties of the matrix and the resulting article as appropriate. Borate may be useful in the matrix.
  • the polymer material can be adjusted.
  • polymers may be included in the material, which have high molecular weights typically above 50,000 or even above 100,000, and vise versa.
  • polymers of varying level of hydrolyses may be used.
  • the cross-linking of the polymers may be increased and/ or the molecular weight may be increased.
  • the polymer used in the elastic article herein has a secondary function, for example a function in the composition wherein article is to be incorporated.
  • the polymer in the polymeric material is a dye transfer inhibiting polymer, dispersant etc.
  • plasticiser which is suitable to aid the formation of a matrix as defined herein can be used. Mixtures of plasticiser may also be used. Preferably, when water is used, an additional plasticiser is present.
  • the plasticiser or at least one of the plasticisers has a boiling point above 40°C, preferably above 60°C, or even above 95°C, or even above 120°C, or even above 150°C.
  • Preferred plasticisers include glycerol or glycerine, glycol derivatives including ethylene glycol, digomeric polyethylene glycols such as diethylene glycol, triethylene glycol and tetraethylene glycol, polyethylene glycol with a weight average M.W.
  • the plasticiser is preferably present at a level of at least 0.5%> by weight of the article, preferably by weight of the matrix, provided that when water is the only plasticiser it is present at a level of at least 3% by weight of the article, or preferably by weight of the matrix.
  • the plasticiser is present at a level of 1% to 35% by weight of the article or matrix, more preferably 2% to 25% or even to 15% or even to 10% or even to 8% by weight of the article or by weight of the matrix.
  • the exact level will depend on the polymeric material and plasticiser used, but should be such that the matrix of the article has the desired Tg.
  • the level is preferably 1% to 10% by weight of the matrix, while when glycerine or ethylene glycol or other glycol derivatives are used, higher levels may be preferred, for example 2% to 15% by weight of the article or matrix.
  • the ratio of plasticiser to polymeric material in the matrix is preferably 1 to 100, more preferably 1 to 70 or 1 to 50, more preferably 1 to 30 or even 1 to 20, again depending on he type of plasticiser and polymeric material used.
  • the ratio is preferably around 1 : 15 to 1 :8, a preferred ratio being around 10: 1.
  • the active ingredient can be any material which is to be delivered to a liquid environment, or preferably an aqueous environment and preferably an ingredient which is active in an aqueous environment.
  • the article when used in cleaning compositions the article can contain any active cleaning ingredients.
  • the articles may also comprise compositions, such as cleaning composition or personal care compositions.
  • the active ingredient is typically a moisture sensitive ingredient, a temperature sensitive ingredient, an oxidizeable ingredient, a volatile ingredient, or a combination thereof.
  • the active ingredient may be biological viable material, hazardous or toxic material an agricultural ingredient such as an agrochemical, a pharmaceutical ingredient such as a medicine or drug, or a cleaning ingredient.
  • active ingredients such as enzymes, perfumes, bleaches, bleach activators, fabric softeners, fabric conditioners, surfactants, such as liquid nonionic surfactant, conditioners, antibacterial agents, effervescence sources, brighteners, photo-bleaches and mixtures thereof.
  • Another active ingredient is a perhydrate bleach, such as metal perborates, metal percarbonates, particularly the sodium salts.
  • organic peroxyacid bleach precursor or activator compound preferred are alkyl percarboxylic precursor compounds of the imide type include the N-,N,N ⁇ N ⁇ tetra acetylated alkylene diamines wherein the alkylene group contains from 1 to 6 carbon atoms, particularly those compounds in which the alkylene group contains 1 , 2 and 6 carbon atoms such as tetraacetyl ethylene diamine (TAED), sodium 3,5,5-tri-methyl hexanoyloxybenzene sulfonate (iso-NOBS), sodium nonanoyloxybenzene sulfonate (NOBS), sodium acetoxybenzene sulfonate (ABS) and pentaacetyl glucose, but also amide substituted alkyl peroxyacid precursor compounds
  • Highly preferred active ingredient for use in the elastic article herein are one or more enzymes.
  • Preferred enzymes include the commercially available lipases, cutinases, amylases, neutral and alkaline proteases, cellulases, endolases, esterases, pectinases, lactases and peroxidases conventionally incorporated into detergent compositions. Suitable enzymes are discussed in US Patents 3,519,570 and 3,533,139.
  • Preferred commercially available protease enzymes include those sold under the tradenames
  • amylases include, for example, ⁇ -amylases obtained from a special strain of B licheniformis, described in more detail in GB-
  • Preferred commercially available amylases include for example, those sold under the tradename Rapidase by Gist-Brocades, and those sold under the tradename Termamyl, Duramyl and BAN by Novo Industries A/S. Highly preferred amylase enzymes maybe those described in PCT/ US 9703635, and in WO95/26397 and WO96/23873.
  • the lipase may be fungal or bacterial in origin being obtained, for example, from a lipase producing strain of Humicola sp., Thermomyces sp. or Pseudomonas sp.
  • Pseudomonas pseudoalcaligenes or Pseudomas fluorescens Lipase from chemically or genetically modified mutants of these strains are also useful herein.
  • a preferred lipase is derived from Pseudomonas pseudoalcaligenes, which is described in Granted European Patent, EP-B-0218272.
  • Another preferred lipase herein is obtained by cloning the gene from Humicola lanuginosa and expressing the gene in Aspergillus oryza, as host, as described in European Patent Application, EP-A-0258 068, which is commercially available from Novo Industri A/S, Bagsvaerd, Denmark, under the trade name Lipolase. This lipase is also described in U.S. Patent 4,810,414, Huge-Jensen et al, issued March 7, 1989.
  • the elastic article of the invention can be made by any process of making a polymer matrix of the defined Tg from a polymeric material and a plasticiser, and combining an active ingredient with such a matrix.
  • Preferred processes involve chemically or physically introducing a gas in a mixture of the polymeric material and plasticiser and optionally the active ingredient.
  • a preferred process for making the article herein comprising the step of a) obtaining a mixture of a polymeric material and a plasticiser, preferably water and an additional plasticiser; b) chemically or physically introducing gas in said mixture of polymeric material and water; c) prior to step b) and/or simultaneously with step b) and/ or subsequently to step b), addition of the active ingredient to the mixture of polymer material and water; d) shaping of articles of the resulting mixture of step c); whereby one or more of steps a) to d) are followed or accompanied by removal of part of the water, if present.
  • Step c) preferably comprises the step of obtaining a body comprising the active ingredient or part thereof and enclosing said body with the mixture of step b).
  • the mixture is preferably an aqueous mixture or slurry and after or in step b), c) and/ or d), part of the water is removed such that the resulting article comprises 3% by weight of free-moisture, or more.
  • the article comprises open and/ or closed cells and the process comprising the steps of a) formation of a mixture of the polymeric material, the active material, a plasticiser and a liquid, whereby the liquid and the plasticiser may be the same compound; b) shaping of bodies from the mixture of claim b) and b) evaporation of the liquid or part thereof to form spacings in the mixture which form the inner area of the cells of the article, whereby step c) is preferably conducted by freeze drying or by heating the bodies, thereby causing the liquid or part thereof to evaporate.
  • Step b) may also be conducted by submitting the mixture of a) to pressure, preferably under mixing and/ or increasing the temperature, and subsequently removing the pressure or part thereof, thereby causing the liquid to evaporate.
  • an extrusion process can be used.
  • the mixture of the polymeric material, plasticiser, preferably including water, and optionaly the active ingredient is introduced in an extruder, wherein the mixture is further mixed and heated, due to the mixing or due to applying heat, preferably such that the mixture therein forms a melt, and then dropping the pressure at the exit point where the extruded mixture (which can be formed into the desired form, for example granules) exits the extruder, whereby the liquid or part thereof evaporates, or preferably the water evaporates as steam from the extruded mixture.
  • Step b) in the process may also be conducted by heating the mixture to cause the liquid or part thereof to evaporate, resulting in the formation of spacings, as above. This can preferably done by feeding the mixture into a spray drying tower, preferably such that the mixture is fed through spray nozzles which form droplets of the mixture, and spray drying the droplets at conventional, resulting in granules of the elastic article.
  • drying steps are preferably followed by a drying step or an additional drying step to remove excess liquid or part thereof, such as water.
  • the drying step is at least done after the polymer matrix is formed, and optionally after the active ingredient is added, preferably as final step in the process.
  • the drying step is done preferably such that the final elastic article is of about the same volume after the drying step as before the drying step.
  • the drying step is preferably done by freeze-drying, whereby the solvent, e.g. water, is removed under vacuum and reduced temperatures. Also useful can be slow fluid bed drying or oven drying at modestly increased temperatures, such as 40- 80°C, or even 40-60°C .
  • Preferred processes involve at least the step of formation of a mixture of polymeric material and a liquid, preferably a solution of polymeric material and a solvent, preferably comprising water, and adding a plasticiser (or as the case may be, additional plasticiser) to this. If the presence of the active ingredient in the matrix is required, this is also added to the mixture of polymeric material solvent and palsticiser. Alternatively, or in addition, it may be preferred that the matrix is formed around the active material, preferably a core of the active material and carrier material.
  • Shaping steps include granulation steps such as atomisation or spray-drying, extrusion, micro pastillisation. Freeze drying is a preferred process to dry the bodies to form the articles.
  • a first preferred process is as follows:
  • the required amount of a solution of the polymer material is obtained, and for example (introduced) in a mix tank.
  • the required amount of (a solution of) the active material for example an enzyme solution is added and the required amount of plasticiser is added, and optionally other additional ingredients, such as stabilisers, fillers, densification agents etc.
  • a gas such as air can be introduced into the solution, by any of the methods above, preferably physically, by high sheer mixing.
  • particles are formed from this mixture by atomisation, preferably using a Positive Displacement pump to transfer the mixture solution to a spray nozzle (s), preferably using either single or multi-fluid nozzles to create liquid droplets.
  • a Positive Displacement pump to transfer the mixture solution to a spray nozzle (s), preferably using either single or multi-fluid nozzles to create liquid droplets.
  • the liquid droplets are then frozen, preferably by passing through a refrigeration media (can include liquid nitrogen, freon, refrigeration oils). Then, the frozen particles are transferred to a vacuum chamber, preferably having a temperature (as measured on the surface of the particles) below 0°C.
  • a refrigeration media can include liquid nitrogen, freon, refrigeration oils.
  • the frozen particles are preferably collected from the spray column and transferred without raising the temperature.
  • the temperature of the walls and contact trays of the freeze dryer are preferably maintained below OC to keep the particles frozen.
  • a vacuum is applied, and the frozen ice crystals will sublimate a gas form, resulting in cells in the particle.
  • the total drying degree can be controlled with the level of vacuum, and contact temperature of the chamber walls and trays.
  • the particles After the particles have been dried to the desired moisture content, they will be free flowing. Then preferably, the particles can be classified via a variety of screens and or process equipment.
  • the atomizing nozzle should preferably be located in a spray column with sufficient height to accomplish droplet freezing while gravity falling.
  • the nozzle type can be of various designs - single fluid pressure nozzle, spinning insert, sonic, or multi-fluid nozzle.
  • the important aspect is to disrupt the liquid stream to form discrete liquid droplets. As these droplets fall with gravity, they need to be cooled to freezing.
  • the freezing media is preferably non-aqueous gas or liquid which can provide rapid freezing of the liquid droplets.
  • the actual temperatures for cooling these droplets to form particles is preferably below 0°C and preferably below -20°C.
  • a gas preferably CO 2 gas
  • the mixture is introduced in a spray drying tower, as above, thereby forming spray-dried foamed particles, which can be classified if necessary.
  • a gas preferably CO 2 gas
  • the inlet temperature in the tower is about 130°C and the outlet temperature about 75°C and the spray rate is 12.5g/min.
  • a Niro Mobil Minor with two fluid nozzles can be used hereby.
  • the resulting particle may be already of the required form, or may be submitted to further freeze drying under vacuum.
  • Another preferred process is as follows:
  • a solution of the polymer material is obtained (or alternatively, a powdered polymer can be used provided a liquid is added) and for example introduced in a mix tank. Then the required amount of plasticiser is added, and optionally other additional ingredients, such as stabilisers, fillers, densification agents etc. This is agitated to become a homogeneous mixture.
  • a gas such as air can be introduced into the solution, by any of the methods above, preferably physically, by high sheer mixing.
  • particles comprising the active ingredient and optionally other ingredients, such as fillers or carriers are prepared, for example by fluid bed coating, by charging first 'cores' (typically when the actives care enzymes, these core particles are sugar or starch particles), to a fluid bed and spraying the active material or a solution of the active material onto these cores and then drying any solvent such as water from the active solution off with warm fluidizing air.
  • first 'cores' typically when the actives care enzymes, these core particles are sugar or starch particles
  • the polymeric mixture above is introduced onto these active/cores , for example via a positive displacement pump leading to an atomizing nozzle inside the fluid bed as described above. More than one nozzle can be used and it may be preferred that different ingredients are added to the core via different nozzles.
  • the fluidizing air needs is preferably below 0°C, preferably around -20°C. Then, the fluidizing air freezes the polymeric mixture/solution onto the outside of the active-core. This is a critical parameter to control and typically the air temperature must be below 0°C in order to quickly freeze the polymeric mixture/solution onto the core particles.
  • the frozen particles thus obtained are transferred to a vacuum chamber, as above, and also classification may take place.
  • the required amount of a solution of the polymer material (or solid polymer and a suitable amount of liquid) is obtained, and for example introduced in a mix tank.
  • the required amount of (a solution of) the active material for example an enzyme solution is added (into the mix tank) and the required amount of plasticiser is added, and optionally other additional ingredients, such as stabilisers, fillers, densification agents.
  • a gas such as air can be introduced into the solution, by any of the methods above, preferably physically, by high sheer mixing.
  • the polymeric solution is pumped from the mix tank into an extruder or into a cavity with a die plate at the end.
  • gas can be injected into the mixture and for example be dispersed via a mechanical shear mixer or a static mixer.
  • the change in pressure creates a slight puffing or swelling in the extrudate.
  • the extrudate is then cut to the correct length with either a die face cutter or with some other device (eg. heated wire, rotating plug cutter, etc.).
  • the extrudates can optionally go through additional rounding steps to become more spherical. Process equipment that can accomplish this function include (rotating pans, agglomeration pans, marumirizers, tumbling drums, mixing drums, etc.) .
  • a paste is prepared by mixing 75g PVOH, 15g Citric acid, 2g PEO and 22.5 g glycerol in a Braun mixer, high sheer, namely set at full speed for 40seconds: then 80g H2O and 80g enzyme was added and mixed at high sheer, namely set at full speed until a smooth foam had formed, approximately within 2mins.
  • the foam was extruded from a 10ml syringe onto a plastic sheet. This was left for 24 hours to dry. Once dry the foam strips were cut into approximately 1 - 2mm sections to form particles of the formula (dry) 63.2 polyvinyl alcohol, 19% glycerol, 12.7
  • the resulting particles had an elastic modulus of 0.00016GN.m " ".
  • the resulting particles give 0%> dusting when tested in a stressed Heubach test, which indicated a very good impact robustness.
  • the stressed Heubach test is performed as known in the art, using equipment as supplied by Heubach Engineering GMbH, Germany, with the stressed modification of the rotation speed of the impeller being 75 + 1 rpm and the balls being of Tungsten carbide and 82 grams each.).
  • a highly preferred process involves shaping particles of mixtures as described above by use of a mould; whereby mixtures as described herein are introduced in a mould and subsequently dried (freeze dried). Also preferred is such a process which uses pastille making equipment, whereby mixtures as described above, preferably comprising also introduced gas, are forced through a rotating perforated drum onto a moving conveyor belt, shaping into pastilles (droplets or particles). When dry or hardened, the thus formed particles or beads are removed from the conveyor belt by a scraper.
  • the first step is to make a mixture of polymeric material and plasticiser, a liquid component, and optionally the active ingredient.
  • gas is introduced into this mixture as described herein. This must preferably be free from large undissolved particles which may block up the perforations in the drum.
  • the mixture is preferably in the temperature range 0-50°C.
  • the mixture is pumped into a manifold that enters the rotating perforated drum and is parallel to the longitudinal axis of the drum.
  • the mixture is pumped into the inner of the drum and, as the drum rotates, is brought into contact with an internal scraper bladed lying in contact and along the length of the inner surface of the perforated drum, parallel to the feed manifold.
  • the distance of the outside surface of the perforated drum is within the height of the desired particle height (which is less than the diameter of the perforations) but not touching a moving conveyor belt or a rotating smooth surfaced drum at the point where the internal scraper is in contact with the inner surface of the perforated drum, the tangential speed of the perforated drum matched by the speed of the conveyor belt or the tangential speed of the smooth surfaced drum.
  • the perforations which are typically in the size range 300 - 2000 ⁇ m (but may be smaller or larger)
  • the rotation of the perforated drum shears the feed material away from the material on the smooth surface thus leaving a droplet, or pastille, which will form the required particle.
  • pastilles can be set by either chilling or by evaporation of some or all of the solvent fluid. If chilling is required the temperature of the conveyor belt or smooth surfaced drum may be in the range ambient to -20°C. If evaporation of a solvent is required, then this can be achieved by heat conduction from the conveyor belt which may be in the range ambient to 70°C, by drying air (which may be heated up to 200°C to reduce drying time) passing over the surface of the pastilles, or both.
  • the resulting particles had a elastic modulus of O.OOlGN.m "2 .
  • the resulting particles give 0% dusting when tested in a stressed Heubach test, which indicated a very good impact robustness.
  • the stressed Heubach test is performed as known in the art, using equipment as supplied by Heubach Engineering GMbH, Germany, with the stressed modification of the rotation speed of the impeller being 75 + 1 rpm and the balls being of Tungsten carbide, 82 grams each.
  • Anoliier example of making foamed articles of the invention, in the form of tablets, beads or particles, is as follows:
  • Apparatus Microbalance, graduated 100ml flask, Kenwood " chefs food processor with provided whisk and mixing bowl, glass or plastic moulds, spatula.
  • Glycerol 99 %, Aldrich chemicals
  • Citric Acid Aldrich, Citric Acid, USP Anhydrous
  • distilled water dry ice (or solid phase CO 2 ), thermally insulated box.
  • the active ingredients for example from 2-10 gram of enzyme, are progressively added to the foam under a maintained mechanical mixing so that a uniform active foam is obtained.
  • Any active ingredient can be added in step 5, at any level, normally up to about 50 grams, for example fabric softeners, bleaching species, nonionic surfactants.
  • foamed articles of the invention in the form of tablets, beads or particles, is as follows:
  • Any active ingredient can be added in step 4, at any level, normally up to about 50 grams, for example fabric softeners, bleaching species, nonionic surfactants.
  • the gas introduced is carbon dioxide, CO 2 . This was done my introducing actual CO 2 gas into the polymer material/ plasticiser but this could equally be done by ingredients (such as effervescence sources) which chemically form CO 2 in the mixture.
  • the elastic article can be made into any form, by any conventional shaping method, some methods being described in detail above. Preferred may be that the elastic article is in the form of a particles, including pastilles and beads or in the form of tablets.
  • the particles can be made by any granulation method, for example by granulation techniques such as atomisation, use of moulds or pastillisation equipment, grinding larger shapes of the elastic article, spray-drying, extrusion, as also described above.
  • Preferred elastic particles herein have a mean particle size of from 10 to 5000 microns, more preferably from 50 to 4000 microns or even to 2000 microns, even more preferably from 100 to 1500 microns or even form 200 or even 300 microns to 1000 microns.
  • the article herein may have a layered structure, having for example, a core of the active ingredient, enclosed by a layer of matrix, optionally coated or for example, a core of (part of) the matrix, enclosed with a layer of the active and then coated, for example with more of the matrix.
  • the elastic article may also be in the form of a sheet, which can be obtained by any method, preferably by forming the sheet in a mould, as described above. When the elastic article is in the form of a sheet, the sheet can have any dimension and can be subsequently reduced in size as required. It may be preferred that the sheet has a mean thickness of from of from 0.01 to 400 microns, more preferably from 0.05 to 200 microns, or even more preferably from 0.1 to 100 microns, or even 0.1 to 50 microns. Additional Ingredients
  • the elastic article of the invention may preferably contain additional ingredients, such as process aids, stabilisers, lubricant, dispensing aids, pH regulators, solubi sers, including hydrotropes and disintegrating aids, densification aids, dyes, whitening agents, fillers, antioxidants and scavengers, perfumes
  • additional ingredients such as process aids, stabilisers, lubricant, dispensing aids, pH regulators, solubi sers, including hydrotropes and disintegrating aids, densification aids, dyes, whitening agents, fillers, antioxidants and scavengers, perfumes
  • Preferred additional agents aie in particular effervescence sources, in particular based on organic carboxylic acids and carbonate sources may be the use of citric acid, malic acid, maleic acid, fumaric acid or mixtures thereof, and for example salts (sodium) of percarbonate, carbonate and/ or bicaibonate These may for example be comprised in the matrix Preferred may be that the acid is present in the matrix and the carbonate in a different layer or coie, or vise versa It has been found that in particular the presence of an acidic material improves the dissolution and/or dispersion of the elastic article of the invention upon contact with water, and can also reduce or prevent interactions, leading to for example precipitation, of the polymeric mate ⁇ al in the elastic article with cationic species present in the aqueous medium.
  • Phosphonate-based such as Chelating agents may also be preferred additional ingredients
  • Preferred may also be to incorporate (m the polymer mate ⁇ al) disintegrating polymers or water-swelleable polymers, which aid dissolution of the article.
  • these may form part of the polymeric matrix herein. Examples of such aids are described in EP851025-A and EP466484-A.
  • Perfumes are also preferred ingredients of the article herein.
  • Surfactants may also be added to the article, including certain nonionic surfactants which may also give a lub ⁇ cation affect. It may be preferred that inorganic salts or silicates are present, including zeolites and/ or phosphates.
  • Preferred additional ingredients are also ammonium compounds such as ammonium sulfate, ammonium citrate, and also granular urea, guanidine hydrochloride, gaunidine carbonate, guanidine sulfonate, granular thiourea dioxide,
  • Colouring agent such as iron oxides and hydroxydes, azo-dyes, natural dyes, are also preferred , preferably present at levels of 0.001% and 10%> or even 0.01 to 5% or even 0.05 to 1 % by weight of the article.
  • Highly preferred additional ingredients include urea and/ or inorganic salts.
  • cross-linking agents changing the crosslinking degree of the polymer material in the matrix.
  • Borate may be useful.
  • the article is coated with a coating agent, as known in the art, by any coating process.
  • a coating agent as known in the art, by any coating process.
  • Preferred may be coating agents containing organic acids or salts, inorganic salts, additional polymers, having Tg of higher than 60°C, typically higher than 70°C.
  • the elastic article comprises (as pH-controller or dissolution aid) an acid such as citric acid, acetic acid, acetic acid glacial, fumaric acid, hydrochloric acid, malic acid, maleic acid, tartaric acid, nitric acid, phosphoric acid, sulfuric acid, pelargonic acid, lauric acid.
  • Buffering agent which also boric acid, sodium acetate, sodium citrate, acetic acid, potassium phosphates and the likes.
  • the component of the invention preferably comprises additional ingredients which can improve the dissolution properties of the article herein.
  • Preferred additional ingredient which improve the dissolution of the article herein preferably comprise; a sulfonated compound such as C]-C 4 alk(en)yl sulfonates, Cj-C aryl sulfonates, di iso butyl benzene sulphonate, toluene sulfonate, cumene sulfonate, xylene sulfonate, salts thereof such as sodium salts thereof, derivatives thereof, or combinations thereof, preferably di iso butyl benzene sulphonate, sodium toluene sulfonate, sodium cumene sulfonate, sodium xylene sulfonate, and combinations thereof; and/or a C]-C 4 alcohol such as methanol, ethanol, propanol such as iso-propanol, and derivatives thereof, and combinations thereof, preferably ethanol and/or iso-propanol; and/or a C 4 -
  • the component of the invention preferably comprises additional ingredients which can improve the stability of the active ingredient of the article herein.
  • additional ingredients are typically capable of stabilising the active ingredient of the component herein, this is especially preferred when the active ingredient(s) comprise an oxidative or moisture sensitive active ingredient, such as one or more enzymes. These additional ingredients may also stabilise the matrix of the component herein, and thus indirectly stabilise the active ingredient. These stabilising ingredients are defined herein as "stabilising agents”.
  • the stabilising agent is preferably a compound which stabilises the active ingredient, or matrix, from oxidative and/or moisture degradation during storage.
  • the stabilising agent may be, or comprise, a foam matrix stabiliser.
  • the stabilising agent may be, or comprise, an active ingredient stabiliser, especially an enzyme stabiliser. Stabilising agents which are capable of stabilising the active ingredient indirectly by keeping the foam matrix of the article stable, herein referred to as "foam stabiliser”.
  • Foam stabilisers preferably comprise a surfactant such as a fatty alcohol, fatty acid, alkanolamide, amine oxide, or derivatives thereof, or combinations thereof.
  • the foam stabiliser may comprise betaine, sulfobetaine, phosphine oxide, alkyl sulfoxide, derivatives thereof, or combinations thereof.
  • Other preferred foam stabilisers comprises one or more anions or cations such as mono-, di-, tri- valent, or other multivalent metal ions, preferred are salts of sodium, calcium, magnesium, potassium, aluminium, zinc, copper, nickel, cobalt, iron, manganese and silver, preferably having an anionic counterion which is a sulphate, carbonate, oxide, chloride, bromide, iodide, phosphate, borate, acetate, citrate, and nitrate, and combinations thereof.
  • anions or cations such as mono-, di-, tri- valent, or other multivalent metal ions
  • salts of sodium, calcium, magnesium, potassium, aluminium, zinc, copper, nickel, cobalt, iron, manganese and silver preferably having an anionic counterion which is a sulphate, carbonate, oxide, chloride, bromide, iodide, phosphate, borate, acetate, citrate, and nitrate, and combinations thereof.
  • the foam stabiliser may comprise finely divided particles, preferably finely divided particles having an average particle size of less than 10 micrometers, more preferably less than 1 micrometer, even more preferably less than 0.5 micrometers, or less than 0.1 micrometers.
  • Preferred finely divided particles are aluminosilicates such as zeolite, silica, or electrolytes described hereinbefore being in the form of finely divided particles.
  • the foam stabiliser may comprise agar-agar, sodium alginate, sodium dodecyl sulfate, polyethylene oxide, guar gum, polyacrylate, or derivatives thereof, or combinations thereof.
  • the foam stabiliser may be coating which is separate to the matrix of the article herein.
  • the foam stabiliser typically partially encloses, preferably completely encloses, the article herein or the active ingredient thereof.
  • the coating is typically contacted to, preferable in such a manner as to form a coat on, the active ingredient prior to said active ingredient being contacted to the polymeric material or the plasticiser of the matrix, and preferably being incorporated in the article herein.
  • the coating may typically be contacted to, preferable in such a manner as to form a coat on, the article herein subsequent to the polymeric material and the plasticiser forming the matrix, and preferably subsequent to the active ingredient contacting said matrix or being incorporated in the article herein.
  • Preferred coating comprises polymers, typically selected from polyvinyl alcohols and derivatives thereof, polyethylene glycols and derivatives thereof, polyvinyl pyrrolidone and derivatives thereof, cellulose ethers and derivatives thereof, and copolymers of these polymers with one another or with other monomers or oligomers. Most preferred are PVP (and derivatives thereof) and/ or PEG (and derivatives thereof) and most preferably PVA (and derivatives thereof) or mixtures of PVA with PEG and/ or PVP (or derivatives thereof). These polymers do not form the matrix of the article herein. Thus, these polymers are different to the polymeric materials of the foam matrix.
  • a preferred coating comprises compounds such as glycerol or glycerine, glycol derivatives including ethylene glycol, digomeric polyethylene glycols such as diethylene glycol, triethylene glycol and tetraethylene glycol, polyethylene glycol with a weight average M.W.
  • Preferred stabilising agents that are capable of stabilising the active ingredient directly, especially if said active ingredient comprises one or more enzymes, are defined herein as “active stabilisers” or “enzyme stabilisers”.
  • active stabilisers interact directly with, and stabilise, the active ingredient.
  • Typical active stabilisers for use herein preferably comprise a surfactant.
  • surfactants for use herein are those described hereinbefore as surfactants suitable for use as matrix stabilisers.
  • surfactants suitable for use herein may comprise surfactants such as sodium alky(en)yl sulfonates, sodium alkoxysulfonates, preferred alkoxysulfonates are those comprising from 10 to 18 carbon atoms in any conformation, preferably linear, and having an average ethoxylation degree of from 1 to 7, preferably from 2 to 5.
  • Suitable active stabilisers comprise boric acid, formic acid, acetic acid, and salts thereof. These acid salts preferably comprise counerions such as calcium and/or sodium.
  • Preferred active stabilisers comprise cations such as calcium and or sodium.
  • cations such as calcium and or sodium.
  • active stabilisers comprise small peptide chains averaging from 3 to 20, preferably from 3 to 10 amino acids, which interact with and stabilise the active ingredient, especially enzyme(s).
  • nucleic acid molecules typically comprising from 3 to 300, preferably from 10 to 100 nucleotides.
  • nucleic acid molecules are deoxyribonucleic acid and ribonucleic acid.
  • the nucleic acid molecules may be in the form of a complex with other molecules such as proteins, or may form a complex with the active ingredient of the article herein, especially enzyme(s).
  • Active stabilisers suitable for use herein, especially when the article herein comprises a bleach comprise anti-oxidants and/or reducing agents such as thiosulphate, methionine, urea, thiourea dioxide, guanidine hydrochloride, guanidine carbonate, guanidine sulfamate, monoethanolamine, diethanolamine, triethanolamine, amino acids such as glycine, sodium glutamate, proteins such as bovine serum albumin and casein, tert- butylhydroxytoluene, 4-4,-butylidenebis (6-tert-butyl-3-methyl-phenol), 2,2'-butlidenebis (6-tert-butyl-4-methylphenol), (monostyrenated cresol, distyrenated cresol, monostyrenated phenol, distyrenated phenol, 1,1 -bis (4-hydroxy-phenyl) cyclohexane, or derivatives thereof, or a combination thereof.
  • active stabilisers may comprise a reversible inhibitor of the active ingredient.
  • a reversible inhibitor of the active ingredient especially if the active ingredient comprises one or more enzymes, may form a complex with, and improve the stability of, said active ingredient, and thus, stabilises the active ingredient during storage.
  • the active ingredient is released, typically into a liquid environment, the reversible inhibitor dissociates from the active ingredient and the active ingredient is then able to perform the desired action it is designed or intended to perform.
  • Active stabilisers suitable for use herein may comprise sugars, Typical sugars for use herein include those selected from the group consisting of sucrose, glucose, fructose, raffmose, trehalose, lactose, maltose, derivatives thereof, and combinations thereof.
  • the active stabiliser may also comprise sugar alcohols such as sorbitol, mannitol, inositol, derivatives thereof, and combinations thereof.
  • the active stabiliser is in the form of a coating or barrier which at least partially encloses the article herein or the active ingredient thereof, preferably completely encloses the article herein or the active ingredient thereof, especially an enzyme.
  • compositions comprising the elastic article
  • the elastic article may be incorporated in any compositions which requires active ingredients to be protected against moisture during storage, against chemical reactions with other ingredients, migration or phase separation of ingredients, or protection against physical forces.
  • the elastic article is useful in cleaning compositions, fabric care compositions, personal care compositions, cosmetic compositions, pharmaceutical compositions. These compositions may are typically solid. They may comprise any additional ingredients, including additional amounts of the active ingredients or polymeric material described above.
  • the cleaning compositions typically contain one or more components selected from surfactants, effervescence sources, bleach catalysts, chelating agents, bleach stabilisers, alkalinity systems, builders, phosphate-containing builders, organic polymeric compounds, enzymes, suds suppressors, lime soap, dispersants, soil suspension and anti-redeposition agents, soil releasing agents, perfumes, dyes, dyed speckles, brighteners, photobleaching agents and additional corrosion inhibitors.
  • the article preferably comprise at least one or more softening agents, such as quaternary ammonium compounds and/ or softening clays, and preferably additional agent such as anti-wrinkling aids, perfumes, chelants, fabric integrity polymers.
  • softening agents such as quaternary ammonium compounds and/ or softening clays
  • additional agent such as anti-wrinkling aids, perfumes, chelants, fabric integrity polymers.
  • compositions comprise one or more other ingredient which can reduce dermatitis or compounds which can help the healing of the skin, metal-containing compounds, in particular zinc- containing compounds, vitamins and cortisone 's, and also compounds to soften the skin such as vaseline, glycerin, triethyleneglycol, lanolin, paraffin and another group of polymers extensively employed by pharmaceutical and cosmetic manufactures, as also described herein.
  • compositions, cosmetic compositions and personal care compositions can be of any form and purpose. Preferred are pharmaceutical powders and tablets.
  • the elastic article can also be incorporated in absorbing articles, for example to release the actives of the elastic article to the skin whereto the absorbing articles is applied, when in contact with water, such as body fluids, for example diapers, wipes, catamenials, plaster, bandages.

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  • Emergency Medicine (AREA)
  • Dispersion Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Detergent Compositions (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
EP00967305A 1999-10-05 2000-10-04 Elastische formteile und deren anwendung Withdrawn EP1237997A1 (de)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
GB9923344A GB2355014A (en) 1999-10-05 1999-10-05 Foams and compositions containing these foams
GB9923393 1999-10-05
GB9923393A GB2355008A (en) 1999-10-05 1999-10-05 Foam matrix coating material
GB9923344 1999-10-05
GB0010599 2000-05-03
GB0010599A GB2361928A (en) 2000-05-03 2000-05-03 Elastic packaging or binder material
PCT/US2000/027333 WO2001025323A1 (en) 1999-10-05 2000-10-04 Elastic articles and uses thereof

Publications (1)

Publication Number Publication Date
EP1237997A1 true EP1237997A1 (de) 2002-09-11

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Application Number Title Priority Date Filing Date
EP00967305A Withdrawn EP1237997A1 (de) 1999-10-05 2000-10-04 Elastische formteile und deren anwendung

Country Status (8)

Country Link
EP (1) EP1237997A1 (de)
JP (1) JP2003511502A (de)
CN (1) CN1408005A (de)
AU (1) AU7752500A (de)
BR (1) BR0014498A (de)
CA (1) CA2385164A1 (de)
MX (1) MXPA02003447A (de)
WO (1) WO2001025323A1 (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6617026B2 (en) 2000-10-02 2003-09-09 Novozymes A/S Particles containing active in visco-elastic liquids
US7070820B2 (en) 2000-10-02 2006-07-04 Novozymes A/S Coated particles containing an active
CN1209452C (zh) * 2000-10-02 2005-07-06 诺和酶股份有限公司 粘弹性液体中含有活性物质的微粒
GB2374082A (en) * 2001-04-04 2002-10-09 Procter & Gamble Particles for a detergent product
DK1414956T3 (da) 2001-06-22 2008-03-03 Genencor Int Höjt påvirkningsresistente granula
DE10159499A1 (de) * 2001-12-04 2003-10-02 Henkel Kgaa Wasch- und/oder Reinigungsartikel
AU2003206382B2 (en) * 2002-01-03 2008-01-24 Smithkline Beecham Corporation Novel pharmaceutical dosage forms and method for producing same
EP1490485B1 (de) 2002-03-27 2015-03-04 Novozymes A/S Granulate mit filamentösen schichten
US7419947B2 (en) 2002-03-27 2008-09-02 Novozymes A/S Process for preparing granules with filamentous coatings
CN101153089B (zh) * 2007-09-06 2010-12-01 四川大学 聚乙烯醇极性泡沫塑料及其制备方法
CN110305521A (zh) * 2019-05-28 2019-10-08 桐乡市宏源化工厂(普通合伙) 一种无刺激性气味的泡沫稳定剂及其制备方法

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Publication number Priority date Publication date Assignee Title
JPS5011401B1 (de) * 1970-06-02 1975-05-01
JP2958954B2 (ja) * 1988-02-29 1999-10-06 東洋紡績株式会社 感光性樹脂組成物
US5458884A (en) * 1992-09-10 1995-10-17 Britton; Peter Bioerodible device for administering active ingredients
JP3278922B2 (ja) * 1992-09-16 2002-04-30 凸版印刷株式会社 パルプ発泡シートおよびその製造方法
WO1998012291A2 (en) * 1996-09-18 1998-03-26 The Procter & Gamble Company Laundry additive particle having multiple surface coatings

Non-Patent Citations (1)

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Title
See references of WO0125323A1 *

Also Published As

Publication number Publication date
JP2003511502A (ja) 2003-03-25
MXPA02003447A (es) 2002-08-20
CA2385164A1 (en) 2001-04-12
AU7752500A (en) 2001-05-10
BR0014498A (pt) 2002-06-11
CN1408005A (zh) 2003-04-02
WO2001025323A1 (en) 2001-04-12

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