WO2022207198A1 - Unité de détergent en monodose - Google Patents

Unité de détergent en monodose Download PDF

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Publication number
WO2022207198A1
WO2022207198A1 PCT/EP2022/054722 EP2022054722W WO2022207198A1 WO 2022207198 A1 WO2022207198 A1 WO 2022207198A1 EP 2022054722 W EP2022054722 W EP 2022054722W WO 2022207198 A1 WO2022207198 A1 WO 2022207198A1
Authority
WO
WIPO (PCT)
Prior art keywords
detergent
outer packaging
underside
tablets
detergent tablets
Prior art date
Application number
PCT/EP2022/054722
Other languages
German (de)
English (en)
Inventor
Till Überrück
Peter Schmiedel
Original Assignee
Henkel Ag & Co. Kgaa
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 Henkel Ag & Co. Kgaa filed Critical Henkel Ag & Co. Kgaa
Priority to EP22710015.3A priority Critical patent/EP4314230A1/fr
Publication of WO2022207198A1 publication Critical patent/WO2022207198A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • 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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047—Detergents in the form of bars or tablets
    • C11D17/0052—Cast detergent 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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047—Detergents in the form of bars or tablets
    • C11D17/0065—Solid detergents containing builders
    • C11D17/0073—Tablets
    • C11D17/0078—Multilayered tablets
    • 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
    • C11D17/0047—Detergents in the form of bars or tablets
    • C11D17/0065—Solid detergents containing builders
    • C11D17/0073—Tablets
    • C11D17/0086—Laundry tablets

Definitions

  • the application was based on the object of providing detergent portion units that can be produced using simplified processes, have high product and storage stability, can be made up easily using very small amounts of packaging materials and are an appealing olfactory, visual and/or haptic appeal.
  • the detergent portion units should have a high product performance and be easy and safe to handle for the consumer.
  • the outer packaging is resealable.
  • adhesive, snap-in, snap-in or plug-in elements are suitable as closure elements, with adhesive and plug-in elements being particularly preferred.
  • closure elements are plug-in closures or removable adhesive closures.
  • the outer packaging is made of cardboard.
  • the advantages of cardboard lie in the great variability of the types and grammages available.
  • Preferred cardboards have a grammage of 150 to 400 g/m 2 .
  • the outer packaging has, for example, a water-insoluble cover film, preferably a polyethylene cover film.
  • Water-insoluble cover films are generally suitable for preventing or at least reducing the entry of water or water vapor through the outer packaging into the interior of the outer packaging.
  • water-insoluble cover films are preferably only applied to the outside or inside of the outer packaging. Full-surface coverage is preferred to effectively limit the ingress of moisture.
  • the three-dimensional form of the detergent shaped body can in principle be freely selected; its lateral surface can, for example, be convex, concave or planar. At the same time, however, certain spatial configurations have proven to be particularly advantageous against the background of the producibility, storage and use of the gel bodies.
  • the underside of the detergent tablet has no corners.
  • Preferred gel bodies are therefore characterized by oval undersides or alternatively by ellipsoidal or round, preferably round, undersides.
  • Corresponding detergent tablets with a non-angular underside are also preferred by many consumers because of their appearance. Preference is therefore given, for example, to detergent tablets which have an underside and an upper side which are connected to one another by a cylindrical lateral surface.
  • angular undersides are advantageous since such detergent tablets can be cut up without residues and can be packed in a space-saving manner.
  • preferred detergent tablets therefore have angular undersides, in particular triangular, quadrangular or hexagonal undersides.
  • detergent tablets which have an upper side that is plane-parallel to the underside have also proven to be advantageous.
  • the detergent tablet has an underside and an upper side which have the same geometric shape, the underside and the upper side having the same surface area.
  • Corresponding detergent tablets can, as already described above, be produced in a simple manner, for example by casting plates and then cutting the plates into individual detergent tablets.
  • these detergent shaped bodies can be spatially aligned more easily than gel bodies with a lower body symmetry due to the geometric identity of the top and bottom sides. This applies in particular to detergent tablets which at the same time have an upper side that is plane-parallel to the underside.
  • detergent tablets of this type are circular cylinders, elliptical cylinders, parallelepipeds, rhombohedrons, right or oblique prisms, cuboids or cubes.
  • the group of circular cylinders and elliptical cylinders includes the vertical circular cylinders and elliptical cylinders as well as the oblique circular cylinders and elliptical cylinders.
  • Detergent tablets are preferred due to their simple production by separating them from a sheet in the form of vertical circular cylinders, vertical elliptical cylinders, right prisms, right parallelepipeds or cubes.
  • the detergent shaped bodies are in the form of tablets or comprise tablets.
  • Particularly preferred detergent tablets are cuboid.
  • the cuboid shaped detergent bodies comprise an underside, an upper side and a lateral surface connecting the underside and the upper side. It has also proven advantageous for the stability of the tableted detergent tablets if the edges delimiting the underside and the upper side are chamfered. In order to increase the stability of these shaped bodies, it may also be advisable to round off the edges of the lateral surfaces connecting the undersides and the top sides.
  • the detergent shaped body comprises b1) a dimensionally stable gel body and b2) an encapsulating substance in the form of a tablet, which partially covers the surface of the dimensionally stable gel body.
  • Gel bodies are bodies that exhibit elastic deformation behavior under the action of force. Objects are considered dimensionally stable if they have an inherent dimensional stability that enables them to assume a non-disintegrating three-dimensional shape under the usual conditions of manufacture, storage, transport and handling by the consumer, with this three-dimensional shape also changing over longer periods under the conditions mentioned Time, preferably 4 weeks, particularly preferably 8 weeks and in particular 32 weeks, not changed, i.e. under the usual conditions of production, storage, transport and handling by the consumer in the spatial-geometric shape caused by the production , that is, does not flow.
  • the gel body and the enveloping substance are preferably adhesively bonded to one another.
  • the gel body preferably occupies at least 50% by volume, preferably at least 60% by volume, of the detergent supply form.
  • detergent tablets are preferred in which the gel component forms at least 16%, preferably at least 25% and in particular at least 30% of the total surface area of the detergent tablet.
  • the coating substance covers 10 to 70%, preferably 30 to 65% and in particular 40 to 60% of the surface of the gel body.
  • the water-soluble coating substance covers the surface of the gel body on two opposite sides of the gel body, since this makes it easier for the consumer to handle the detergent portion unit.
  • this type of surface covering has advantages with regard to the packaging of the detergent portion units, in particular when packaging several detergent portion units together, for example when the detergent portion units are stacked in an outer packaging.
  • detergent portion units in which the gel body has an underside and an upper side and the water-soluble coating substance at least partially covers both the underside and the upper side of the gel body. Both the underside and the upper side of the gel body are preferably covered to an extent of at least 40%, preferably at least 60% and in particular at least 80%.
  • the gel body has an underside and an upper side, and the water-soluble coating substance covers both the underside and the upper side of the gel body over the entire surface.
  • the detergent portion units according to the invention are particularly suitable for the formulation of surfactant-containing compositions, since these compositions tend to adhere and stick to a particular extent, for example, when exposed to moisture.
  • the gel body therefore contains 30 to 70% by weight, preferably 40 to 60% by weight and in particular 45 to 55% by weight of surfactant.
  • the gel bodies For the manufacturability and the subsequent dissolving power of the gel bodies, it has proven to be advantageous if they contain 15 to 35% by weight, preferably 20 to 30% by weight, of an aqueous-organic solvent.
  • Preferred gel bodies also contain dye.
  • Preferred detergent dosage units comprise a transparent gel body.
  • Those gel bodies are referred to as “transparent” which have a transmission in the wavelength range from 410 to 800 nm at at least one wavelength, preferably at 600 nm, above 20%, preferably above 30% and in particular above 35%. The transmission is determined by means of VIS spectrometry at a sample temperature of 20° C. and a cuvette length of 10 mm.
  • low-molecular gel formers with a molar mass of up to 2000 g/mol in the gel body, with their proportion by weight of the total weight of the gel body preferably being less than 5% by weight 0.1 to 5% by weight and particularly preferably 0.1 to 2.5% by weight.
  • the low molecular weight gelling agent has a solubility in water of less than 0.1 g/L (20° C.).
  • the solubility of the organic gelator compound is determined at 20°C in double-distilled, demineralized water.
  • gel formers are preferably suitable which have a structure containing at least one hydrocarbon structural unit with 6 to 20 carbon atoms (preferably at least one carbocyclic, aromatic structural unit) and additionally an organic structural unit covalently bonded to the aforementioned hydrocarbon unit, the at least two groups selected from -OH, -NH-, or mixtures thereof.
  • gel bodies are characterized in that said gel bodies contain at least one benzylidene alditol compound of the formula (GB-I) as gel former
  • n 0 or 1
  • m 0 or 1
  • both said benzylidene alditols in the L configuration or in the D configuration or a mixture of both are suitable according to the invention. Because of their natural availability, the benzylidene alditol compounds in the D configuration are preferably used according to the invention.
  • the alditol skeleton of the benzylidene alditol compound according to formula (GB-I) contained in the shaped body is composed of D-glucitol, D-mannitol, D-arabinitol, D-ribitol, D-xylitol, L -glucitol, L-mannitol, L-arabinitol, L-ribitol or L-xylitol.
  • Those gel bodies which are characterized in that R 1 , R 2 , R 3 , R 4 , R 5 and R 6 according to the benzylidene alditol compound of the formula (GB-I) independently of one another are a hydrogen atom, methyl, ethyl, chlorine are particularly preferred , fluorine or methoxy, preferably a hydrogen atom.
  • n according to the benzylidene alditol compound of the formula (GB-I) is preferably 1.
  • m according to the benzylidene alditol compound of formula (GB-I) preferably represents 1.
  • the gel body very particularly preferably contains at least one compound of the formula (GB-11) as the benzylidene alditol compound of the formula (GB-I) wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as defined in formula (I).
  • R 1 , R 2 , R 3 , R 4 , R 5 and R 6 independently represent a hydrogen atom, methyl, ethyl, chlorine, fluorine or methoxy, preferably a hydrogen atom.
  • the benzylidene alditol compound of formula (GB-I) is selected from 1,3:2,4-di-0-benzylidene-D-sorbitol; 1,3:2,4-di-0-(p-methylbenzylidene)-D-sorbitol; 1,3:2,4-di-O-(p-chlorobenzylidene)-D-sorbitol; 1,3:2,4-di-0-(2,4-dimethylbenzylidene)-D-sorbitol; 1,3:2,4-di-0-(p-ethylbenzylidene)-D-sorbitol; 1,3:2,4-di-0-(3,4-dimethylbenzylidene)-D-sorbitol or mixtures thereof.
  • Preferred gel bodies contain at least one 2,5-diketopiperazine compound of the formula (GB-II) as gel former wherein
  • R 1 , R 2 , R 3 and R 4 independently represent a hydrogen atom, a
  • R 5 represents a hydrogen atom, a linear (Ci to C6) alkyl group, a branched (C3 to Cio) alkyl group, a (C3 to C6) cycloalkyl group, a (C2-C6) alkenyl group, a (C2-C6 )- alkynyl group, a (Ci-C 4 )-hydroxyalkyl group, a (Ci-C 4 )-alkoxy-(Ci-C 4 )-alkyl group, a (C1-C 4 )-acyloxy-(Ci-C 4 )- alkyl group, an aryloxy-(Ci-C 4 )-alkyl group, a 0-(aryl-(Ci-C 4 )-alkyl)oxy-(Ci-C 4 )-alkyl group, a (Ci-C 4 )-alkylsulfanyl- (Ci-C 4 ) alkyl group, an ary
  • R 3 and R 4 according to formula (GB-II) stand for a hydrogen atom.
  • R 2 , R 3 and R 4 according to formula (GB-II) stand for a hydrogen atom.
  • Very particularly preferred shaped bodies according to the invention therefore contain at least one 2,5-diketopiperazine compound of the formula (GB-IIa) wherein R 1 and R 5 are as defined under formula (GB-II) (vide supra).
  • radical R 1 according to formula (GB-II) and according to formula (GB-IIa) binds in the para-position of the phenyl ring.
  • the numbers 3 and 6 positioned on the ring atoms in formula (GB-IIb) mark only the positions 3 and 6 of the diketopiperazine ring, as are generally used within the scope of the invention for naming all 2,5-diketopiperazines according to the invention.
  • the 2,5-diketopiperazine compounds of formula (GB-II) have centers of chirality at least at the carbon atoms in positions 3 and 6 of the 2,5-diketopiperazine ring.
  • the Numbering of the ring positions 3 and 6 was illustrated as an example in formula (GB-IIb).
  • the 2,5-diketopiperazine compound of the formula (GB-II) of the compositions according to the invention is preferably the configuration isomer 3S,6S, 3R,6S, 3S based on the stereochemistry of the carbon atoms in the 3- and 6-positions of the 2,5-diketopiperazine ring ,6R, 3R,6R or mixtures thereof, particularly preferably 3S,6S.
  • Preferred gel bodies contain at least one 2,5-diketopiperazine compound of the formula (GB-II) as gelling agent, selected from 3-benzyl-6-carboxyethyl-2,5-diketopiperazine, 3-benzyl-6-carboxymethyl-2,5- diketopiperazine, 3-Benzyl-6-(p-hydroxybenzyl)-2,5-diketopiperazine, 3-Benzyl-6-iso-propyl-2,5-diketopiperazine, 3-Benzyl-6-(4-aminobutyl)-2, 5-diketopiperazine, 3,6-di(benzyl)-2,5-diketopiperazine, 3,6-di(p-hydroxybenzyl)-2,5-diketopiperazine, 3,6-di(p-(benzyloxy)benzyl)- 2,5-diketopiperazine, 3-benzyl-6-(4-imidazolyl)methyl-2,5-diketopiperazine
  • the gel bodies according to the invention may contain at least one diarylamidocystine compound of the formula (GB-III) as gel former a). wherein
  • X + independently represents a hydrogen atom or an equivalent of a cation
  • R 1 , R 2 , R 3 and R 4 independently represent a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a Ci-C 4 alkoxy group, a C 2 -C 4 hydroxyalkyl group, a hydroxyl group, an amino group, an N-(Ci-C 4 -alkyl)amino group, an N,N-di(Ci-C 4 -alkyl)amino group, an N-(C2-C 4 -hydroxyalkyl)amino group, an N,N-di(C 2 -C 4 -hydroxyalkyl)amino group or R 1 with R 2 or R 3 with R 4 forms a 5- or 6-membered fused ring, which in turn each has at least one group from Ci-C 4 -alkyl group, Ci-C 4 -Alkoxy group, C 2 -C 4 -hydroxyalkyl group, hydroxyl group, amino group, N-(Ci-
  • Said gel bodies can contain at least one compound of the formula (GB-III) in which R 1 , R 2 , R 3 and R 4 independently represent a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a Ci-C 4 - Alkoxy group, a C 2 -C 4 hydroxyalkyl group, a hydroxyl group, or R 1 with R 2 or R 3 with R 4 forms a 5- or 6-membered fused ring, which in turn each has at least one group from Ci-C 4 - Alkyl group, Ci-C 4 alkoxy group, C2-C4 hydroxyalkyl group, hydroxyl group may be substituted.
  • R 1 , R 2 , R 3 and R 4 independently represent a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a Ci-C 4 - Alkoxy group, a C 2 -C 4 hydroxyalkyl group, a hydroxyl group, or R 1 with
  • N-(C8-C24) -hydrocarbylglyconamide compounds suitable as gel formers a) preferably have the formula (GB-IV). where n is 2 to 4, preferably 3 or 4, especially 4;
  • R 1 is selected from hydrogen, C1-C16 alkyl, C1-C3 hydroxy or
  • methoxyalkyl radicals preferably C1-C3 alkyl, hydroxyalkyl or methoxyalkyl radicals, particularly preferably methyl;
  • R 2 is selected from Cs-C 24 alkyl, Cs-C 24 monoalkenyl, C8-C24
  • dialkenyl radicals C8-C 24 trialkenyl radicals, Cs-C 24 hydroxyalkyl radicals, Cs-C 24 hydroxyalkenyl radicals, C1-C3 hydroxyalkyl radicals or methoxy-Ci-C3 alkyl radicals, preferably Cs-Cis alkyl radicals and mixtures thereof, more preferably Cs, C10 , C12, C14, C16 and cis-alkyl radicals and mixtures thereof, most preferably C12 and C14 alkyl radicals or a mixture thereof.
  • the group HO-CH2-(CHOH) n -C- is one of one
  • glucuronic acid is to be mentioned in particular as a preferred residue.
  • R 1 is preferably H or a short-chain alkyl radical, especially methyl.
  • R 2 is preferably a long-chain alkyl group, for example a Cs-Cis-alkyl group.
  • the at least one low molecular weight gel former is selected from the group consisting of the cyclic dipeptides, the cyclic dipeptide derivatives and dibenzylidene sorbitol. Due to its technical effect, the at least one gelling agent is particularly preferred, dibenzylidene sorbitol (DBS).
  • DBS dibenzylidene sorbitol
  • the enveloping substance is opaque.
  • Those enveloping substances are referred to as “non-transparent” which have a transmission below 10%, preferably below 5% and in particular below 1% in the wavelength range from 410 to 800 nm at at least one wavelength, preferably at 600 nm.
  • the transmission is determined by means of VIS spectrometry at a sample temperature of 20° C. and a cuvette length of 10 mm.
  • non-transparent enveloping substances creates a product appearance, especially when used in combination with transparent gel bodies, which enables the consumer to distinguish between the surfaces covered by the enveloping substance and those not covered by the enveloping substance and the detergent portion unit, for example when removing it from a container , which comprises several detergent portion units, to specifically grip the surfaces covered by the enveloping substance and in this way to avoid direct contact with the gel body.
  • the gel body and the enveloping substance preferably have a color difference DE of more than 20, preferably more than 40.
  • preferred coating substances are white, ie not colored.
  • the white color of the enveloping substance is particularly suitable for printing.
  • the enveloping substance can also be colored.
  • the colored design of the enveloping substance enables, for example, the optical communication of specific product properties, for example with regard to its effect or smell.
  • the colored enveloping substance preferably does not have the same color as the gel body. Colored enveloping substances can of course also be printed.
  • they can have a film packaging, it being particularly preferred if each of the detergent tablets has a separate film packaging.
  • the water-soluble film material may comprise one or more structurally distinct water-soluble polymer(s).
  • Particularly suitable as water-soluble polymer(s) are polymers from the group of (possibly acetalized) polyvinyl alcohols (PVAL) and their copolymers.
  • Water-soluble film materials are preferably based on a polyvinyl alcohol or a polyvinyl alcohol copolymer whose molecular weight is in the range from 10,000 to 1,000,000 gmof 1 , preferably from 20,000 to 500,000 gmof 1 , particularly preferably from 30,000 to 100,000 gmof 1 and in particular from 40,000 to 80,000 gmof 1 .
  • the preparation of the polyvinyl alcohol and polyvinyl alcohol copolymers typically involves the hydrolysis of intermediate polyvinyl acetate.
  • Preferred polyvinyl alcohols and polyvinyl alcohol copolymers have a degree of hydrolysis of 70 to 100 mol %, preferably 80 to 90 mol %, particularly preferably 81 to 89 mol % and in particular 82 to 88 mol %.
  • preferred polyvinyl alcohol copolymers include an ethylenically unsaturated carboxylic acid, its salt or its ester.
  • Such polyvinyl alcohol copolymers particularly preferably contain, in addition to vinyl alcohol, sulfonic acids such as 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS), acrylic acid, methacrylic acid, acrylic esters, methacrylic esters or mixtures thereof; among the esters, Ci- 4 -alkyl esters or - hydroxyalkyl esters are preferred.
  • sulfonic acids such as 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS), acrylic acid, methacrylic acid, acrylic esters, methacrylic esters or mixtures thereof; among the esters, Ci- 4 -alkyl esters or - hydroxyalkyl esters are preferred.
  • AMPS 2-acrylamido-2-methyl-1-propanesulfonic acid
  • Other suitable monomers are ethy
  • film packaging which consists of at least 40% by weight, preferably at least 60% by weight and in particular at least 80% by weight of polyvinyl alcohol.
  • Particularly preferred detergent tablets therefore do not have an outer packaging made of a water-soluble or water-insoluble film material.
  • detergent supply forms which comprise at least ten, preferably at least twenty, particularly preferably at least thirty detergent tablets have proven to be advantageous.
  • the detergent tablets are preferably arranged sorted in the outer packaging in such a way that each of the detergent tablets is in direct contact with at least one other detergent tablet.
  • the detergent tablets are sorted in the outer packaging so that each of the detergent tablets has at least one rough top or bottom in direct contact with at least one rough top or bottom of another detergent tablet.
  • Such a form of supply is distinguished by high storage and transport stability of the detergent tablets.
  • low adhesion of detergent tablets to one another and to the outer packaging is observed on the one hand, and a low tendency to abrasion of the tablets on the other.
  • the particularly preferred sortings described below are also particularly advantageous for detergent supply forms in which the outer packaging has no water-insoluble cover film on its inside.
  • detergent supply forms comprising a) outer packaging b) detergent tablets with an upper side that is plane-parallel to the underside and a lateral surface connecting the upper side and the lower side, the detergent tablets having a rectangular lower side whose largest diagonal is more than double, preferably more than four times is the height of the detergent tablet, wherein i) the outer packaging contains at least ten, preferably at least twenty, particularly preferably at least thirty detergent tablets, which are sorted in the outer packaging, and ii) the detergent tablets have an upper side or an underside, the average roughness of which is between 10pm and 500pm, where iii) the detergent tablets are sorted in the outer packaging so that - at least 25% of the detergent tablets have their underside in direct contact with the bottom surface of the outer packaging,
  • All detergent tablets with at least one rough top or bottom are in direct contact with at least one rough top or bottom of another detergent tablet.
  • a detergent presentation form comprising a) outer packaging with a base surface, a top surface opposite the base surface and side surfaces connecting the base surface and the top surface, b) detergent tablets with an upper side that is plane-parallel to the underside and a lateral surface connecting the upper side and the underside, wherein the detergent tablets have a rectangular underside, the largest diagonal of which is more than twice, preferably more than four times, the height of the detergent tablet, wherein i) the outer packaging contains at least two, preferably at least four, particularly preferably at least eight detergent tablets, which are sorted in the outer packaging are arranged, and ii) the detergent tablets have an upper side or an underside with an average roughness of between 10 ⁇ m and 500 ⁇ m, iii) the detergent tablets being sorted in the outer packaging are arranged in such a way that that
  • all detergent shaped bodies are in direct contact with the side surface of the outer packaging with their upper side and lower side.
  • items provided by this application include:
  • Detergent supply form comprising a) outer packaging b) detergent tablets with an upper side, an underside and a lateral surface connecting the upper side and the lower side, wherein i) the outer packaging contains at least two detergent tablets, which are sorted in the outer packaging, and ii) the detergent tablets one have a rough upper side or a rough underside, the mean roughness of which is from 1 ⁇ m to 1000 ⁇ m, preferably from 10 ⁇ m to 800 ⁇ m and in particular from 25 to 500 ⁇ m.
  • the detergent tablets having a weight of 14 g to 42 g, preferably 20 g to 38 g, in particular 24 g to 34 g.
  • Detergent dosage form according to one of the previous points, wherein the detergent shaped bodies are in the form of tablets or comprise tablets.
  • Detergent supply form comprises at least ten, preferably at least twenty, particularly preferably at least thirty detergent tablets.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent shaped body has a flat underside, the largest diagonal of which is greater than the height of the detergent shaped body.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent tablets have a flat underside, the largest diagonal of which is 1.5 times, preferably more than 2 times, the height of the gel body.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent molding has an oval underside.
  • Detergent molding has an ellipsoidal or round, preferably a round underside.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent tablet has a square bottom.
  • Detergent tablet has a triangular, square or hexagonal underside.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent tablet has a top side that is plane-parallel to the underside.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent tablet has a bottom and a top, which have the same geometric shape and the bottom and the top have the same surface area.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent tablet has a bottom and a top, which have the same geometric shape and the bottom and the top have different surface areas.
  • Detergent offer form according to one of the previous points, wherein the
  • Detergent molding is cuboid.

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

Abstract

L'invention concerne une forme de présentation de détergent comprenant a) un conditionnement extérieur, b) des corps façonnés détergents ayant une face supérieure, une face inférieure et une surface de couverture reliant la face supérieure et la face inférieure ; i) le conditionnement extérieur contient au moins deux corps façonnés détergents qui sont disposés d'une manière triée dans le conditionnement extérieur, et ii) les corps façonnés détergents ont une face supérieure rugueuse ou une face inférieure rugueuse, dont la rugosité moyenne est de 1 µm à 1 000 µm, de préférence de 10 µm à 800 µm et en particulier de 25 à 500 µm.
PCT/EP2022/054722 2021-04-01 2022-02-24 Unité de détergent en monodose WO2022207198A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP22710015.3A EP4314230A1 (fr) 2021-04-01 2022-02-24 Unité de détergent en monodose

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102021203326.1 2021-04-01
DE102021203326.1A DE102021203326A1 (de) 2021-04-01 2021-04-01 Waschmittelportionseinheit

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DE19955240A1 (de) * 1999-11-17 2001-05-23 Henkel Kgaa Verfahren zur Herstellung von Wasch- und Reinigungsmittelformkörpern
EP1121306A1 (fr) * 1998-03-30 2001-08-08 The Procter & Gamble Company Produit sous emballage comportant des comprimes
WO2002086047A1 (fr) * 2001-04-25 2002-10-31 Henkel Kommanditgesellschaft Auf Aktien Elements moules de produits de lavage a phase viscoelastique
US6677296B2 (en) * 1999-12-16 2004-01-13 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Washing tablets marked with indicia on their surfaces
WO2006105841A1 (fr) * 2005-04-04 2006-10-12 Unilever Plc Comprimes de traitement de linge multiphase -
WO2021013515A1 (fr) * 2019-07-24 2021-01-28 Unilever N.V. Conditionnement pour doses unitaires

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GB0514951D0 (en) 2005-07-21 2005-08-24 Unilever Plc A packaged product for multi-phase laundry tablets
DE102015213943A1 (de) 2015-07-23 2017-01-26 Henkel Ag & Co. Kgaa Wasch- oder Reinigungsmittel umfassend wenigstens zwei Phasen

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1121306A1 (fr) * 1998-03-30 2001-08-08 The Procter & Gamble Company Produit sous emballage comportant des comprimes
DE19955240A1 (de) * 1999-11-17 2001-05-23 Henkel Kgaa Verfahren zur Herstellung von Wasch- und Reinigungsmittelformkörpern
US6677296B2 (en) * 1999-12-16 2004-01-13 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Washing tablets marked with indicia on their surfaces
WO2002086047A1 (fr) * 2001-04-25 2002-10-31 Henkel Kommanditgesellschaft Auf Aktien Elements moules de produits de lavage a phase viscoelastique
WO2006105841A1 (fr) * 2005-04-04 2006-10-12 Unilever Plc Comprimes de traitement de linge multiphase -
WO2021013515A1 (fr) * 2019-07-24 2021-01-28 Unilever N.V. Conditionnement pour doses unitaires

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DE102021203326A1 (de) 2022-10-06

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