GB2367828A - Water-soluble containers containing aqueous compositions - Google Patents

Water-soluble containers containing aqueous compositions Download PDF

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Publication number
GB2367828A
GB2367828A GB0020965A GB0020965A GB2367828A GB 2367828 A GB2367828 A GB 2367828A GB 0020965 A GB0020965 A GB 0020965A GB 0020965 A GB0020965 A GB 0020965A GB 2367828 A GB2367828 A GB 2367828A
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United Kingdom
Prior art keywords
water
composition
film
aqueous composition
container
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.)
Granted
Application number
GB0020965A
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GB0020965D0 (en
GB2367828B (en
Inventor
Paul John Duffield
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.)
Reckitt Benckiser UK Ltd
Reckitt Benckiser Healthcare UK Ltd
Original Assignee
Reckitt and Colman Products Ltd
Reckitt Benckiser UK Ltd
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 Reckitt and Colman Products Ltd, Reckitt Benckiser UK Ltd filed Critical Reckitt and Colman Products Ltd
Priority to GB0020965A priority Critical patent/GB2367828B/en
Publication of GB0020965D0 publication Critical patent/GB0020965D0/en
Priority to GB0120479A priority patent/GB2368587A/en
Priority to MXPA03001581A priority patent/MXPA03001581A/en
Priority to US10/362,631 priority patent/US20040023826A1/en
Priority to ES01960955T priority patent/ES2312464T3/en
Priority to US10/364,000 priority patent/US7271141B2/en
Priority to CN01814646.5A priority patent/CN1608126A/en
Priority to AU8417501A priority patent/AU8417501A/en
Priority to JP2002521618A priority patent/JP2004507579A/en
Priority to CA002419280A priority patent/CA2419280C/en
Priority to AU8234101A priority patent/AU8234101A/en
Priority to EP01963142A priority patent/EP1311440B1/en
Priority to AU2001282341A priority patent/AU2001282341B2/en
Priority to PCT/GB2001/003827 priority patent/WO2002016222A1/en
Priority to AT01963142T priority patent/ATE493345T1/en
Priority to BR0113489-2A priority patent/BR0113489A/en
Priority to CA2420121A priority patent/CA2420121C/en
Priority to DE60143752T priority patent/DE60143752D1/en
Priority to AU2001284175A priority patent/AU2001284175B2/en
Priority to ES01963142T priority patent/ES2357884T3/en
Priority to EP01960955A priority patent/EP1311654B1/en
Priority to GB0120487A priority patent/GB2368588B/en
Priority to PL359935A priority patent/PL204786B1/en
Priority to DE60136545T priority patent/DE60136545D1/en
Priority to PCT/GB2001/003821 priority patent/WO2002016541A1/en
Priority to AT01960955T priority patent/ATE414134T1/en
Publication of GB2367828A publication Critical patent/GB2367828A/en
Application granted granted Critical
Publication of GB2367828B publication Critical patent/GB2367828B/en
Priority to ZA200301300A priority patent/ZA200301300B/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/042Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
    • C11D17/043Liquid or thixotropic (gel) compositions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65BMACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
    • B65B9/00Enclosing successive articles, or quantities of material, e.g. liquids or semiliquids, in flat, folded, or tubular webs of flexible sheet material; Subdividing filled flexible tubes to form packages
    • B65B9/02Enclosing successive articles, or quantities of material between opposed webs
    • B65B9/04Enclosing successive articles, or quantities of material between opposed webs one or both webs being formed with pockets for the reception of the articles, or of the quantities of material
    • B65B9/042Enclosing successive articles, or quantities of material between opposed webs one or both webs being formed with pockets for the reception of the articles, or of the quantities of material for fluent material
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates

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

Abstract

Water-soluble containers contain aqueous compositions having a free water content of greater than 3 wt%. The container is of thermoformed PVA film. The composition may be a dishwashing, water-softening, laundry, disinfectant, antibacterial or antiseptic. By the presence of the water in the composition the container is given a fuller appearance.

Description

IMPROVEMENTS IN OR RELATING TO AQUEOUS COMPOSITIONS The present invention relates to water-soluble containers containing aqueous compositions.
It is known to package chemical compositions which may be of a hazardous or irritant nature in water soluble or water dispersible material such as films. The package can simply be added to water in order to dissolve or disperse the contents of the package into the water.
For example, WO 89/12587 discloses a package which comprises an envelope of a water soluble or water dispersible material which comprises a flexible wall and a water-soluble or water-dispersible heat seal.
The package may contain an organic liquid comprising, for example, a pesticide, fungicide, insecticide or herbicide.
It is also known to package detergents in watersoluble or water-dispersible containers. For example, WO 94/14941 discloses a water-soluble or waterdispersible capsule containing an aqueous dishwasher detergent. The capsule is made of gelatin.
CA-A-1, 112, 534 discloses a packet made of a watersoluble material in film form enclosing within it a paste-form, automatic dishwasher-compatible detergent composition. The water-soluble material may be, for example, poly (vinyl alcohol), polyethylene oxide or methyl cellulose. Example 1 illustrates an embodiment wherein a poly (vinyl alcohol) (PVOH) film is made into a 5cm square packet by heat sealing its edges, and the packet is filled with a composition which contains 8.5 wt. % water.
In fields such as detergents for domestic use, an attractive appearance for an article is extremely
desirable. However, in the prior art such as that described above, a bag is simply formed from a single sheet of water soluble film. The film is folded and three of the edges are heat-sealed to form the bag.
The bag is then filled and the remaining edge heat sealed. This produces a rather flat, limp envelope containing the product. Furthermore there may be a lack of uniformity between different bags because of their flexible nature.
We have discovered that this type of product is not deemed to be attractive by an average consumer.
The present invention seeks to provide a water soluble container containing an aqueous composition, which container has a more attractive appearance. In particular the container should be relatively selfsupporting and look full. Ideally the container should have an attractive, rounded three-dimensional appearance.
It is known to form water-soluble containers by thermoforming a water-soluble material. For example, WO 92/17382 discloses a package containing an agrochemical such as a pesticide comprising a first sheet of non-planar water-soluble or water-dispersible material and a second sheet of water-soluble or waterdispersible material superposed on the first sheet and sealed to it by a continuous closed water-soluble or water-dispersible seal along a continuous region of the superposed sheets. It is stated to be advantageous to ensure that the package produced is evacuated of air or the contents are under reduced pressure to provide increased resistance to shock.
Furthermore, when the package contains a liquid, the liquid must be an organic liquid which must be reasonably dry and typically contains less than 2 to 3% of water to ensure that it does not attack the water-soluble package and cause leakage.
EP-A-654, 418 describes self-standing flexible pouches which may contain, for example, liquid detergent compositions for refilling other containers. In order to avoid folding of the pouch, which can lead to cracking and leakage, the bag is inflated before it is sealed.
In order to improve the strength of packages containing liquids, it is also known to provide the package with residual inflatability. Thus, for example, EP-A-524,721 describes a water-soluble package which contains a liquid, wherein the package is inflatable to a volume which is greater than the initial volume of the package. Thus the package is filled to less than its complete capacity, and the unused capacity may be partially, but not totally, filled with a gas such as air. The unused capacity which does not contain gas provides the residual inflatability.
We have now surprisingly discovered a water-soluble container which contains a liquid composition can be given an attractive three-dimensional appearance by using a thermoforming technique such as that disclosed in WO 92/17382 on a PVOH film and ensuring that the liquid composition has a water content which is greater than that used before. Immediately after the containers are prepared, they have a limp, unattractive appearance. However, after storage for a short while, for example from a few minutes to a few hours, they develop a more attractive threedimensional appearance, and also appear to look fuller. They can also be said to have a"puffed-up" appearance. Although not bound by this theory, it is believed that the water in the aqueous composition shrinks the PVOH film, which was stretched during the thermoforming process, around the liquid composition to provide the attractive appearance.
The present invention accordingly provides a watersoluble container containing an aqueous composition, wherein: a) the container comprises a thermoformed PVOH film; and b) the aqueous composition contains greater than 3 wt% free water, based on the weight of the aqueous composition.
The present invention also provides the use of a thermoformed PVOH film to package an aqueous composition containing greater than 3 wt% water, based on the weight of the aqueous composition.
The present invention further provides a process for producing a container as defined above which comprises : a) thermoforming a first PVOH film to produce a pocket; b) filling the pocket with the aqueous composition; c) placing a second PVOH film on top of the filled pocket; and d) sealing the first film and second film together.
There is no direct correlation between the actual amount of water present in a composition and the amount of free water as required in the present invention. Free water includes water which is not available to the PVOH film such as water held within a gelled matrix or water of solvation of any components present in the composition.
In order to determine the amount of free water present in a composition, a standard loss-on-drying determination test may be carried out. A sample of the composition, usually about 10 g, is weighed, and then maintained at 60 C for 3 hours under a partial
vacuum of 200 mbar (20 kPa). The sample is then reweighed, and the weight lost determined. In the present invention, the loss on drying must be greater than 3 wt%, preferably greater than 4,5, 6,7, 8,9, 10,11, or 12 wt%, even more preferably greater than 20 wt% or greater than 30 wt%.
The method of forming the container is similar to the process described in WO 92/17382. A first PVOH film is initially thermoformed to produce a non-planar sheet containing a pocket, such as a recess, which is able to retain the aqueous composition. The pocket is generally bounded by a flange, which is preferably substantially planar. The pocket may have internal barrier layers as described in, for example, WO 93/08095. The pocket is then filled with the aqueous composition, and a second PVOH film is placed on the flange and across the pocket. The second PVOH film may or may not be thermoformed. If the first film contains more than one pocket, the second film may be placed across all of the pockets for convenience. The pocket may be completely filled, or only partly filled, for example to leave an air space of from 2 to 20%, especially from 5 to 10%, of the volume of the container immediately after it is formed. Partial filling may reduce the risk of rupture of the container if it is subjected to shock and reduce the risk of leakage if the container is subjected to high temperatures.
The films are then sealed together, for example by heat sealing across the flange. Other methods of sealing the films together may be used, for example infra-red, radio frequency, ultrasonic, laser, solvent, vibration or spin welding. An adhesive such as an aqueous solution of PVOH may also be used. The seal desirably is also water-soluble.
If more than one container is formed at the same time,
the packaged compositions may then be separated from each other by cutting the flanges. Alternatively, they may be left conjoined and, for example, perforations provided between the individual containers so that they can be easily separated at a later stage, for example by a consumer.
If the containers are separated, the flanges may be left in place. However, desirably the flanges are partially removed in order to provide an even more attractive, three-dimensional appearance. Generally the flanges remaining should be as small as possible for aesthetic purposes while bearing in mind that some flange is required to ensure the two films remain adhered to each other. A flange having a width of 1 mm to 5 mm is desirable, preferably 1.5 mm to 2.5 mm, most preferably about 2 mm.
The containers may then be left for a while to attain their attractive appearance, or may be immediately packaged into boxes for retail sale, and left to attain their attractive appearance in the boxes. The containers may themselves be packaged in outer containers if desired, for example non-water soluble containers which are removed before the water soluble containers are used.
If more than one PVOH film is used for the containers, the films may be identical or different. The PVOH film may be partially or fully alcoholised or hydrolysed, for example, it may be from 40 to 100%, preferably 70 to 92%, more preferably about 88%, alcoholised or hydrolysed, polyvinyl acetate film. The film may be cast, blown or extruded. It may also be unorientated, mono-axially oriented or bi-axially oriented.
The film is generally cold water (200C) soluble, but, depending on its degree of hydrolysis, may be
insoluble in cold water at 200C and only become soluble in warm water or hot water having a
temperature of, for example, 30oC, 40oC, 500C or even 60OC. If the film is soluble in cold water, or water at a temperature of up to, say, 35 C steps must be taken to ensure that the aqueous composition contained inside the container does not dissolve the film from the inside. Steps may be taken to treat the inside surface of the film, for example by coating it with an agent such as poly (vinyl dichloride) or PTFE (polytetrafluoroethylene), or to adapt the composition to ensure that it does not dissolve the film. For example, it has been found that ensuring the composition has a high ionic strength or contains an agent which minimises water loss through the walls of the container will prevent the composition from dissolving the PVOH film from the inside. This is described in more detail in EP-A-518,689 and WO 97/27743.
It is particularly important to avoid pinholes in the film through which leakage of the contained composition may occur. It may therefore be appropriate to use a laminate of two or more layers of a different or the same PVOH film, as pinholes are unlikely to coincide in two layers of material.
When a first and second PVOH film are used to form the containers of the present invention, the first PVOH film will generally have a thickness before
thermoforming of 20 to 500 Am, especially 70 to 400 m, for example 70 to 300 Am, most preferably 70 to 160 m, especially 75 to 100 Am. The thickness of the second PVOH film may be less than that of the first film as the second film will not generally be thermoformed so localised thinning of the sheet will not occur. The thickness of the second film will generally be from 20 to 160 Am, preferably from 50 to 100 AM.
The films may be chosen, if desired, such that they have the same thickness before the first film is
thermoformed, or have the same thickness after the first sheet has been thermoformed in order to provide a composition which is encapsulated by a substantially constant thickness of film.
The containers of the present invention generally contain from 5 to 100 g of aqueous composition, especially from 15 to 40 g, depending on their intended use. For example, a dishwashing composition may weigh from 15 to 20g, a water-softening composition may weigh from 25 to 35g, and a laundry composition may weigh from 30 to 40g.
The containers may have any shape achievable by thermoforming. For example they can take the form of a cylinder, cube or cuboid, i. e. a rectangular parallelepiped whose faces are not all equal. In general, because the containers are not rigid, the sides are not planar, but rather are convex. If the container is formed from a thermoformed PVOH film and a planar PVOH film, the seam between the two films will appear nearer one face of the container rather than the other. Apart from the deformation of the container due to the shrinkage of the PVOH film discussed above, deformation may also occur at the stage of manufacture if desired. For example, if the pocket is filled with a gelled composition having a height greater than that of the pocket, the second film will be deformed when placed on top of the pocket.
In general the maximum dimension of the filled part of the container (excluding any flanges) is 5 cm. For example, a rounded cuboid container may have a length of 1 to 5 cm, especially 3.5 to 4.5 cm, a width of 1.5 to 3.5 cm, especially 2 to 3 cm, and a height of 1 to 2 cm, especially 1.25 to 1.75 cm.
The container of the present invention desirably
contains an aqueous composition which is a dishwashing, water-softening, laundry or detergent composition or a rinse aid. In this case the container is preferably suitable for use in a domestic washing machine such as a laundry washing machine or a dishwashing machine. The composition may also be a disinfectant, antibacterial or antiseptic composition intended to be diluted with water before use, or a concentrated refill composition, for example for a trigger-type spray used in domestic situations. Such a composition can simply be added to water already held in the spray container.
The composition contains greater than 3 wt% free water based on the weight of the aqueous composition, in order to ensure that the container has an attractive appearance. However, the actual amount of water present in the composition may be in excess of the amount of free water since the total water content includes water of solvation and water held within a gelled matrix. The total amount of water is generally more than 5 wt%, for example more than 10,15, 20,25 or 30 wt%. The total water content may be less than 80 wt%, for example less than 70,60, 50,40 wt%. It may, for example, contain from 30 to 65 wt% total water.
The remaining ingredients of the aqueous composition depend on the use of the composition. Thus, for example, the compositions may contain surface active agents such as an anionic, nonionic, cationic, amphoteric or zwitterionic surface active agents or mixtures thereof.
Examples of anionic surfactants are straight-chained or branched alkyl sulfates and alkyl polyalkoxylated sulfates, also known as alkyl ether sulfates. Such surfactants may be produced by the sulfation of higher C8-C20 fatty alcohols.
Examples of primary alkyl sulfate surfactants are those of formula : ROSOM wherein R is a linear C8-C hydrocarbyl group and M is a water-solubilising cation. Preferably R is C1O-C16 alkyl, for example Cl2-Cl4, and M is alkali metal such as lithium, sodium or potassium.
Examples of secondary alkyl sulfate surfactants are those which have the sulfate moiety on a "backbone" of the molecule, for example those of formula:
CH, (CH2) n (CHOSO3-M+) (CH2) mCH3 wherein m and n are independently 2 or more, the sum of m+n typically being 6 to 20, for example 9 to 15, and M is a water-solubilising cation such as lithium, sodium or potassium.
Especially preferred secondary alkyl sulfates are the (2,3) alkyl sulfate surfactants of formulae: CH2 (CH2)x (CHOSO3-M+)CH3 and CH3 (CH2)x(CHOSO3-M+)CH2CH3 for the 2-sulfate and 3-sulfate, respectively. In these formulae x is at least 4, for example 6 to 20, preferably 10 to 16. M is cation, such as an alkali metal, for example lithium, sodium or potassium.
Examples of alkoxylated alkyl sulfates are ethoxylated alkyl sulfates of the formula:
RO (C2H4OSOS 3- < wherein R is a Ca-C2o alkyl group, preferably CO-C, 8 such as a C12-C16'n is at least 1, for example from 1 to 20, preferably 1 to 15, especially 1 to 6, and M is a salt-forming cation such as lithium, sodium,
potassium, ammonium, alkylammonium or alkanolammonium.
These compounds can provide especially desirable fabric cleaning performance benefits when used in combination with alkyl sulfates.
The alkyl sulfates and alkyl ether sulfates will generally be used in the form of mixtures comprising varying alkyl chain lengths and, if present, varying degrees of alkoxylation.
Other anionic surfactants which may be employed are salts of fatty acids, for example Ca-Cl8 fatty acids, especially the sodium, potassium or alkanolammonium salts, and alkyl, for example Ce-C18, benzene sulfonates.
Examples of nonionic surfactants are fatty acid alkoxylates, such as fatty acid ethoxylates, especially those of formula: R (C, H, O) OH wherein R is a straight or branched Ce-C16 alkyl group,
preferably a Cg-Cg, for example C-C or Cl2-Cl4, alkyl group and n is at least 1, for example from 1 to 16, preferably 2 to 12, more preferably 3 to 10.
The alkoxylated fatty alcohol nonionic surfactant will frequently have a hydrophilic-lipophilic balance (HLB) which ranges from 3 to 17, more preferably from 6 to 15, most preferably from 10 to 15.
Examples of fatty alcohol ethoxylates are those made from alcohols of 12 to 15 carbon atoms and which contain about 7 moles of ethylene oxide. Such materials are commercially marketed under the trademarks Neodol 25-7 and Neodol 23-6.5 by Shell Chemical Company. Other useful Neodols include Neodol 1-5, an ethoxylated fatty alcohol averaging 11 carbon
atoms in its alkyl chain with about 5 moles of ethylene oxide ; Neodol 23-9, an ethoxylated primary Cl2-Cl3 alcohol having about 9 moles of ethylene oxide; and Neodol 91-10, an ethoxylated C9-C11 primary alcohol having about 10 moles of ethylene oxide.
Alcohol ethoxylates of this type have also been marketed by Shell Chemical Company under the Dobanol trademark. Dobanol 91-5 is an ethoxylated Cg-Cll fatty alcohol with an average of 5 moles ethylene oxide and
Dobanol 25-7 is an ethoxylated C-Cg fatty alcohol with an average of 7 moles of ethylene oxide per mole of fatty alcohol.
Other examples of suitable ethoxylated alcohol nonionic surfactants include Tergitol 15-S-7 and Tergitol 15-S-9, both of which are linear secondary alcohol ethoxylates available from Union Carbide Corporation. Tergitol 15-S-7 is a mixed ethoxylated product of a C11-C15 linear secondary alkanol with 7 moles of ethylene oxide and Tergitol 15-S-9 is the same but with 9 moles of ethylene oxide.
Other suitable alcohol ethoxylated nonionic surfactants are Neodol 45-11, which is a similar ethylene oxide condensation products of a fatty alcohol having 14-15 carbon atoms and the number of ethylene oxide groups per mole being about 11. Such products are also available from Shell Chemical Company.
Further nonionic surfactants are, for example, C-Cl8 alkyl polyglycosides, such as C12-C16 alkyl polyglycosides, especially the polyglucosides. These are especially useful when high foaming compositions are desired. Further surfactants are polyhydroxy fatty acid amides, such as C10-C18 N-(3-methoxypropyl) glycamides and ethylene oxide-propylene oxide block polymers of the Pluronic type.
Examples of cationic surfactants are those of the quaternary ammonium type.
Examples of amphoteric surfactants are CIO-C,,, amine oxides and the C12-C betaines and sulfobetaines.
The total content of surfactants in a laundry or detergent composition is desirably 60 to 95 wt%, especially 75 to 90 wt%. Desirably an anionic surfactant is present in an amount of 50 to 75 wt%, the nonionic surfactant is present in an amount of 5 to 20 wt%, the cationic surfactant is present in an amount of from 0 to 10 wt% and/or the amphoteric surfactant is present in an amount of from 0 to 10 wt%. The amounts are based on the total solids content of the composition, i. e. excluding the water which is present.
The compositions, particularly when used as laundry washing or dishwashing compositions, may also comprise enzymes, such as protease, lipase, amylase, and cellulase enzymes. Such enzymes are commercially available and sold, for example, under the registered trade marks Esperase, Alcalase, Savinase, Termanyl, Lipolase and Celluzyme by Nova Nordisk A/S. Desirably the enzymes are present in the composition in an amount of from 0.5 to 3 wt%, especially 1 to 2 wt%.
The compositions may, if desired, comprise a thickening agent or gelling agent. Suitable thickeners are polyacrylate polymers such as those sold under the trade mark CARBOPOL, or the trade mark ACUSOL by Rohm and Hass Company. Other suitable thickeners are xanthan gums. The thickener, if present, is generally present in an amount of from 0.2 to 4 wt%, especially 0.5 to 2 wt%.
Dishwasher compositions usually comprise a detergency
builder. Suitable builders are alkali metal or ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, bicarbonates, borates, polyhydroxysulfonates, polyacetates, carboxylates such as citrates, and polycarboxylates. The builder is desirably present in an amount of up to 90 wt%, preferably 15 to 90 wt%, more preferably 15 to 75 wt%, relative to the total content of the composition.
Further details'of suitable components are given in, for example, EP-A-694,059, EP-A-518,720 and WO 99/06522.
The compositions can also optionally comprise one or more additional ingredients. These include conventional detergent composition components such as further surfactants, bleaches, bleach enhancing agents, builders, suds boosters or suds suppressors, anti-tarnish and anti-corrosion agents, organic solvents, co-solvents, phase stabilisers, emulsifying agents, preservatives, soil suspending agents, soil release agents, germicides, phosphates such as sodium tripolyphosphate or potassium tripolyphosphate, pH adjusting agents or buffers, non-builder alkalinity sources, chelating agents, clays such as smectite clays, enzyme stabilizers, anti-limescale agents, colourants, dyes, hydrotropes, dye transfer inhibiting agents, brighteners, and perfumes. If used, such optional ingredients will generally constitute no more than 10 wt%, for example from 1 to 6 wt%, the total weight of the compositions.
The builders counteract the effects of calcium, or other ion, water hardness encountered during laundering or bleaching use of the compositions herein. Examples of such materials are citrate, succinate, malonate, carboxymethyl succinate, carboxylate, polycarboxylate and polyacetyl carboxylate salts, for example with alkali metal or alkaline earth metal cations, or the corresponding
free acids. Specific examples are sodium, potassium and lithium salts of oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, ClO-C22 fatty acids and citric acid. Other examples are organic phosphonate type sequestering agents such as those sold by Monsanto under the trade mark Dequest and alkylhydroxy phosphonates. Citrate salts and C12-C18 fatty acid soaps are preferred.
Other suitable builders are polymers and copolymers known to have builder properties. For example, such materials include appropriate polyacrylic acid, polymaleic acid, and polyacrylic/polymaleic and copolymers and their salts, such as those sold by BASF under the trade mark Sokalan.
The builders generally constitute from 0 to 3 wt%, more preferably from 0.1 to 1 wt%, by weight of the compositions.
Compositions which comprise an enzyme may optionally contain materials which maintain the stability of the enzyme. Such enzyme stabilizers include, for example, polyols such as propylene glycol, boric acid and borax. Combinations of these enzyme stabilizers may also be employed. If utilized, the enzyme stabilizers generally constitute from 0.1 to 1 wt% of the compositions.
The compositions may optionally comprise materials which serve as phase stabilizers and/or co-solvents.
Example are C1-C3 alcohols or diols such as methanol, ethanol, propanol and 1,2-propanediol. Cl-C3 alkanolamines such as mono-, di-and triethanolamines and mono isopropanolamine can also be used, by themselves or in combination with the alcohols.
The compositions may optionally comprise components which adjust or maintain the pH of the compositions at
optimum levels. Examples of pH adjusting agents are NaOH and citric acid. The pH may be from, for example, 1 to 13, such as 8 to 11 depending on the nature of the composition. For example, a dishwashing composition desirably has a pH of 8 to 11, a laundry composition has a pH of 7 to 9, and a water-softening composition desirably has a pH of 7 to 9.
One or more than one phase may be present. For example the container may be filled with an aqueous composition and a liquid composition which is immiscible with the aqueous composition. It may also be filled with an aqueous composition and a separate solid composition, for example in the form of a ball or pill.
The present invention will now be further explained in the following Examples.
Example 1 A dishwashing composition was prepared by mixing together the following components in the weight proportions indicated: Potassium tripolyphosphate powder 12% Sodium tripolyphosphate powder 30% Isothiazolinone 0.1% Polyacrylate thickener (Carbopol) 1% Nonionic surfactant 0.5% Sodium citrate 10% Dehardened water 46.4% A Multivac thermoforming machine operating at 6 cycles/min and at ambient conditions of 25 C and 35% RH (5% RH) was used to thermoform a PVOH film. This was Monosol M8534 obtained from Chris Craft Inc, Gary, Indiana, USA, having a degree of hydrolysis of 88% and a thickness of 100 jum. The PVOH film was thermoformed
into a rectangular mould of 39mm length, 29mm width and 16mm depth, with the bottom edges being rounded to a radius of 10mm, at 115-118 C. The thus formed pocket was filled with 10 ml of the dishwashing
composition, and a 75 m thick Monosol M8534 PVOH film was placed on top and heat sealed at 144-148 C. The thus produced containers were separated from each other by cutting the flanges. Each container was initially limp, but attained an attractive, rounded
appearance after a few minutes.
Example 2 The following formulations were prepared by mixing together the indicated components in the weight proportions indicated. In all instances the compositions were filled into containers following the procedure described in Example 1, and containers having an attractive, rounded appearance were obtained.
A laundry detergent composition: Sodium carbonate 20% Nonylphenol ethoxylate 10% Accusol 820 obtainable from Rohm and Haas Company 3.3% Sodium citrate 5% Dehardened water 61.7% An automatic dishwasher detergent : Sodium citrate 8% Van Gel ES thickener obtainable from R. T. Vanderbilt Company 4% Tetrapotassium pyrophosphate 10% Sodium tripolyphosphate 30% Anhydrous sodium metasilicate 2% Sodium xylene sulfonate 2.25%
Deceth-4-phosphate 0. 75% Dehardened water 43% A heavy duty laundry liquid : Neodol 25-7 C12-1S linear alcohol 18% Biosoft D-62 sodium alkylbenzenesulfonate 5.5% Sodium carbonate 2% Anhydrous sodium metasilicate 5% Tetrapotassium pyrophosphate 20% Sodium citrate 7.5% Carbopol ETDZ691 polymer obtainable from Goodrich 0.5% Dehardened water 41.5% A slurry-type laundry detergent : Sodium carbonate 40% Sodium citrate 4.8% Accusol 820 obtainable from Rohm and Haas 2% Accusol 810 obtainable from Rohm and Haas 4% Sodium tripolyphosphate 10% Accusol 445 obtainable from Rohm and Haas 2% Nonylphenol ethoxylate 10% Dehardened water 27.2% A dishwashing composition : Accusol 810 11% Accusol 445N 4% Sodium tripolyphosphate 20% Tetrapotassium pyrophosphate 10% Potassium silicate 29% Triton CF-32 alkylamine ethoxylate 3% Potassium citrate 5% Dehardened water 18%

Claims (11)

1. A water-soluble container containing an aqueous composition, wherein: a) the container comprises a thermoformed poly (vinyl alcohol) film; and b) the aqueous composition contains greater than 3 wt% free water, based on the weight of the aqueous composition.
2. A container according to claim 1 wherein the aqueous composition is a dishwashing, water-softening, laundry or detergent composition or is a rinse-aid.
3. A container according to any one of the preceding claims which is suitable for use in a domestic washing machine.
4. A container according to claim 1 wherein the aqueous composition is a disinfectant, antibacterial or antiseptic composition.
5. A container according to claim 1 wherein the aqueous composition is a refill composition for a trigger-type spray.
6. A container according to any one of the preceding claims wherein the aqueous composition comprises more than 6 wt% free water.
7. A container according to claim 6 wherein the aqueous composition comprises more than 20 wt% free water.
8. A container according to any one of the preceding claims which is soluble in water at room temperature (200C).
9. A container according to any one of the preceding claims which comprises two poly (vinyl alcohol) films sealed together.
10. Use of a thermoformed poly (vinyl alcohol) film to package an aqueous composition containing greater than 3 wt% free water, based on the weight of the aqueous composition.
11. A process for producing a container as defined in any one of claims 1 to 9 which comprises: a) thermoforming a first poly (vinyl alcohol) film to produce a pocket; b) filling the pocket with the aqueous composition; c) placing a second poly (vinyl alcohol) film on top of the filled pocket; and d) sealing the first film and second film together.
GB0020965A 2000-08-25 2000-08-25 Water-soluble containers containing aqueous compositions Expired - Fee Related GB2367828B (en)

Priority Applications (27)

Application Number Priority Date Filing Date Title
GB0020965A GB2367828B (en) 2000-08-25 2000-08-25 Water-soluble containers containing aqueous compositions
AT01963142T ATE493345T1 (en) 2000-08-25 2001-08-23 WATER-SOLUBLE HOT-FORMED CONTAINERS CONTAINING AQUEOUS COMPOSITIONS
DE60143752T DE60143752D1 (en) 2000-08-25 2001-08-23 WATER-RELATED HOT-MOLDED CONTAINERS CONTAINING AQUEOUS COMPOSITIONS
BR0113489-2A BR0113489A (en) 2000-08-25 2001-08-23 Water-soluble packaging containing liquid compositions
ES01960955T ES2312464T3 (en) 2000-08-25 2001-08-23 WATER SOLUBLE CONTAINERS CONTAINING LIQUID COMPOSITIONS.
US10/364,000 US7271141B2 (en) 2000-08-25 2001-08-23 Water soluble packages containing liquid compositions
CN01814646.5A CN1608126A (en) 2000-08-25 2001-08-23 Water soluble packages containing liquid compositions
AU8417501A AU8417501A (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers comprising aqueous compositions
JP2002521618A JP2004507579A (en) 2000-08-25 2001-08-23 Water-soluble package containing liquid composition
CA002419280A CA2419280C (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
AU8234101A AU8234101A (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
EP01963142A EP1311440B1 (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers comprising aqueous compositions
AU2001282341A AU2001282341B2 (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
PCT/GB2001/003827 WO2002016222A1 (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers comprising aqueous compositions
GB0120479A GB2368587A (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers for aqueous compositions
US10/362,631 US20040023826A1 (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers comprising aqueous compositions
CA2420121A CA2420121C (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers comprising aqueous compositions
DE60136545T DE60136545D1 (en) 2000-08-25 2001-08-23 WATER-SOLUBLE PACKAGING CONTAINS LIQUID COMPOSITIONS
AU2001284175A AU2001284175B2 (en) 2000-08-25 2001-08-23 Water-soluble thermoformed containers comprising aqueous compositions
ES01963142T ES2357884T3 (en) 2000-08-25 2001-08-23 WATER SOLUBLE THERMOFORMED CONTAINERS THAT INCLUDE WATER COMPOSITIONS.
EP01960955A EP1311654B1 (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
GB0120487A GB2368588B (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
PL359935A PL204786B1 (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
MXPA03001581A MXPA03001581A (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions.
PCT/GB2001/003821 WO2002016541A1 (en) 2000-08-25 2001-08-23 Water-soluble packages containing liquid compositions
AT01960955T ATE414134T1 (en) 2000-08-25 2001-08-23 WATER SOLUBLE PACKAGINGS CONTAINING LIQUID COMPOSITIONS
ZA200301300A ZA200301300B (en) 2000-08-25 2003-02-18 Water-soluble package containing liquid compositions.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB0020965A GB2367828B (en) 2000-08-25 2000-08-25 Water-soluble containers containing aqueous compositions

Publications (3)

Publication Number Publication Date
GB0020965D0 GB0020965D0 (en) 2000-10-11
GB2367828A true GB2367828A (en) 2002-04-17
GB2367828B GB2367828B (en) 2002-10-09

Family

ID=9898292

Family Applications (1)

Application Number Title Priority Date Filing Date
GB0020965A Expired - Fee Related GB2367828B (en) 2000-08-25 2000-08-25 Water-soluble containers containing aqueous compositions

Country Status (3)

Country Link
ES (1) ES2357884T3 (en)
GB (1) GB2367828B (en)
ZA (1) ZA200301300B (en)

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WO2004022692A1 (en) * 2002-08-14 2004-03-18 Henkel Kommanditgesellschaft Auf Aktien Portioned cleaning agent or detergent composition
WO2004031034A1 (en) * 2002-09-26 2004-04-15 Henkel Kommanditgesellschaft Auf Aktien Shrunken moulded detergent bodies
GB2405828A (en) * 2003-09-12 2005-03-16 Reckitt Benckiser Nv Improvements in or relating to containers using a thermoforming process
WO2005058700A1 (en) * 2003-12-19 2005-06-30 Reckitt Benckiser N.V. Injection moulded containers
WO2005121302A1 (en) * 2004-06-11 2005-12-22 Reckitt Benckiser N.V. Process for preparing water-soluble articles
WO2008087424A1 (en) * 2007-01-18 2008-07-24 Reckitt Benckiser N.V. Dosage element and a method of manufacturing a dosage element
WO2014086506A1 (en) * 2012-12-05 2014-06-12 Henkel Ag & Co. Kgaa Low-in-water to water-free liquid cleaning agents

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WO2004022692A1 (en) * 2002-08-14 2004-03-18 Henkel Kommanditgesellschaft Auf Aktien Portioned cleaning agent or detergent composition
US7375070B2 (en) 2002-08-14 2008-05-20 Henkel Kommanditgesellschaft Auf Aktien Portioned detergent composition
WO2004031034A1 (en) * 2002-09-26 2004-04-15 Henkel Kommanditgesellschaft Auf Aktien Shrunken moulded detergent bodies
DE10244803B4 (en) * 2002-09-26 2012-03-22 Henkel Ag & Co. Kgaa Shrunken detergent tablets
GB2405828A (en) * 2003-09-12 2005-03-16 Reckitt Benckiser Nv Improvements in or relating to containers using a thermoforming process
WO2005058700A1 (en) * 2003-12-19 2005-06-30 Reckitt Benckiser N.V. Injection moulded containers
WO2005121302A1 (en) * 2004-06-11 2005-12-22 Reckitt Benckiser N.V. Process for preparing water-soluble articles
EP2752481A1 (en) * 2004-06-11 2014-07-09 Reckitt Benckiser N.V. Process for preparing water-soluble articles
WO2008087424A1 (en) * 2007-01-18 2008-07-24 Reckitt Benckiser N.V. Dosage element and a method of manufacturing a dosage element
US8980817B2 (en) 2007-01-18 2015-03-17 Reckitt Benckiser N.V. Dosage element and a method of manufacturing a dosage element
US10294446B2 (en) 2007-01-18 2019-05-21 Reckitt Benckiser Finish B.V. Dosage element and a method of manufacturing a dosage element
WO2014086506A1 (en) * 2012-12-05 2014-06-12 Henkel Ag & Co. Kgaa Low-in-water to water-free liquid cleaning agents

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GB2367828B (en) 2002-10-09
ZA200301300B (en) 2004-04-02
ES2357884T3 (en) 2011-05-03

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