[0001] The present invention refers to a package unit comprising shaped or granular item(s)
and a cardboard container having a childproof closure to avoid that children have
undesired access to said item(s).
[0002] Detergent compositions or water softener compositions commonly comprise a variety
of components which are to be avoided to have contact with human skin, eyes or mucosa.
During the last years an increasing consumer interest could be seen to use pre-portioned
quantities of consumer products like e.g. detergent or cleaning compositions to avoid
incorrect dosing or unneeded high amounts of said product. To comply with this desire
pre-dosed portions of detergent compositions commonly are offered in form of a tablet,
a pouch, a sachet or similar, wherein said portions may comprise one, but also two,
three or more different partial compositions provided as separate layers or regions
of a tablet or in separate chambers of a pouch or sachet.
[0003] To provide - besides handling comfort and reliable dosing - an attractive appearance
to said pre-dosed portions the producers tend to give the portioned (partial) compositions
a special design or shape. This, however, also piques children's curiosity and children
are interested in touching and tasting the sometimes nicely colored small packages
or tablets.
[0004] To meet this problem there are several approaches provided by the producers to prevent
children from coming in undesired contact with harmful compounds. Most of the package
systems including childproof closure systems involve plastic materials offering relatively
reliably locking systems. However, due to increasing awareness of environmental problems
the requirement to save plastic materials in consumer goods is coming to the force.
[0005] The state of the art provides also childproof packages made of cardboard, in particular
in the area of packaging pharmaceutical tablets. Most of these childproof systems
are working with the principle of a "locked drawer", thus, an arresting block has
to be unlocked by one or two fingers to pull a drawer out of a cover. Such systems
are described e.g. in
EP1 002 744 A1,
US 7,090,079 B2,
WO 2005/049437 A1 and
US 5,275,291.
[0006] The principle of a drawer, however, are for larger systems like the packaging of
detergent compositions not very comfortable and further quite material-consuming.
[0008] In all the before-mentioned solutions at least a part of the packaging system is
still made of plastic material, e.g. the blister trays inside the package, further
all of said packages realize a principle wherein much packaging material is needed.
[0009] Thus, it was an object of the present invention to provide a package for shaped or
granular items avoiding as far as possible any plastic material, providing a childproof
closure to bar children from contact with said items without making production and
/ or handling of said package and its content too difficult or extensive.
[0010] This object is met by a package unit comprising (i) a cardboard container having
an upper top surface (1), a bottom 2) and at least three side surfaces (3), wherein
on one of said top (1) or side surfaces (3) a childproof closure (4) is provided,
wherein said closure (4) is made of cardboard and is slidely movable between a position
closing the container and a position providing an opening (O) allowing the removal,
discharge, pouring or taking out of the content of said container, and (ii) shaped
or granular items, comprising (a) a detergent or cleaning composition, or (b) a water
softener composition.
[0011] The package container is prepared essentially as a whole from cardboard, paperboard
and/or paper. Preferably the container is prepared from corrugated cardboard, e.g.
single wall double faced corrugated cardboard; or a double wall corrugated cardboard
or triple wall corrugated cardboard having paper sheets at least on both outer surfaces
("faced cardboard"), wherein the use of a single wall double faced corrugated cardboard
is preferred.
[0012] According to the present application the term "cardboard" is used for a material
commonly also described as "paperboard". It should be agreed that these terms can
be used synonymously, not providing a noticeable difference in the material suitable
for the present invention.
[0013] In the following it should be understood, that when the term "cardboard" is used,
this means as well and in particular a corrugated cardboard, wherein said corrugated
cardboard further may optionally comprise a vapor or moisture barrier layer.
[0014] Said cardboard preferably comprises a vapor or moisture barrier layer, preferably
"inside" the cardboard, which means that said barrier layer is provided between the
both outer surface layers. Said vapor or moisture barrier layer may be a layer provided
attached to or applied to one of the surfaces of the paper sheets used for preparation
of the corrugated cardboard, wherein said layered surface is then faced to the inner
side of the cardboard, or said barrier layer is provided as a separate film, sheet
or layer, which is included into the corrugated cardboard during its preparation.
Furthermore, also a "solid" cardboard may be used, e.g. a cardboard laminate including
a vapor or moisture barrier layer sandwiched between two cardboard sheets, between
a cardboard and a paper sheet or between two paper sheets, or a cardboard laminate
comprising only a cardboard sheet and a barrier layer, however due to the weight,
rigidity and comfort the use of corrugated cardboard panels is preferred.
[0015] The vapor or moisture barrier layer can be provided in form of a film, e.g. a film
of a material known in the art for such barrier layers. Examples of suitable materials
are polyethylene (PE), like high density polyethylene or low density polyethylene;
polyethylene terephthalate (PET); polyvinyl alcohol (PVOH); polyvinyl acetate (PVA);
polypropylene (PP), polylactic acid (PLA) and/or polyamide (PA), which can be used
as single polymers, mixture of polymers or copolymers of the mentioned, wherein PE
films are particularly preferred. Furthermore, an oiled paper may be used as a vapor
or moisture barrier sheet.
[0016] Further, the moisture barrier layer can be provided as a coating on at least one
surface of a sheet used for preparation of the cardboard or the package container
of the present invention. Such coatings may comprise at least one of: (i) a wax compound,
(ii) a surfactant, in particular a surfactant solid 20°C (iii) a polymer, (iv) a triazine-containing
compound; (v) a nano-cellulose material; (vi) a nanoclay material; and/or (vii) an
inorganic oxide material. Presence of at least one of compounds (i), (ii) or (iii)
is preferred
[0017] The thickness of the barrier film or layer typically ranges from about 5 nanometers
to about 100 µm, preferably from 10 nm to 50 µm, 20 nm to 25 µm, 30 nm to 10 µm, 40
nm to 5 µm or 50 nm to1 µm.
[0018] Examples of wax compounds (i) are natural waxes, in particular wax esters or wax
alcohols. Examples for such waxes are lanolin, paraffine, carnauba wax, candelilla
wax or bees wax, wax alcohols may be represented by cetyl alcohol, carnaubyl alcohol,
ceryl alcohol and myricyl alcohol, examples of waxy acids are myristinic acid, palmic
acid, stearic acid, laurinic acid, lignoceric acid, cerotinic acid, montanic acid
and melissic acid, without being restricted to the mentioned.
[0019] Examples of suitable surfactants (ii) are nonionic or anionic surfactants which are
solid at room temperature (defined being 20°C), preferably which are solid up to a
temperature of 35°C. Due to their characteristics nonionic surfactants are preferred,
in particular fatty alcohols or esters, optionally comprising EO or PO groups. Such
surfactants are disclosed in detail below as part of the detergent composition.
[0020] Suitable polymers (iii) are those as mentioned above for the barrier film and further
copolymers including styrene butadiene copolymers, modified styrene butadiene copolymers,
styrene/acrylate copolymers, carboxylated polystyrene, acrylic/polyacrylic polymers,
polyvinylacetate-ethylene, polyvinyl acrylic polymer, soy protein polymer; corn zein
(protein), starch, a polyolefin dispersion (e.g., modified propylene-based dispersion),
polyvinylidene chloride, polylactic acid, polyhydroxyalkanoate polymers, polybutylene
succinate, plasticized cellulose acetate, and mixtures thereof.
[0021] Triazine compounds (iv) that can be included are 1,3,5-triazines such as melamine,
ammeline, ammelide, cyanuric acid, 2-ureidomelamine, melam, melem, melon, melamine
salts such as, for example, melamine cyanurate, melamine phosphate, dimelamine pyrophosphate
or melamine polyphosphate and functionalized melamines, such as for instance hexamethoxymethyl
melamine or acrylate-functionalized melamine.
[0022] An example for a suitable cellulose material (v) is nano-fibrillated or nanocrystalline
cellulose (NCC). The barrier layer may comprise nanocrystalline cellulose which is
a uniform, redispersible natural nanoparticle obtained from the crystalline regions
of cellulose fibers. The cellulose can be derived from natural cellulose such as wood
or wheat straw. Alternatively, the cellulose can be derived from a regenerated source
such as rayon or viscose. Exemplary nanocrystalline cellulose is available from CELLUFORCE™
of Montreal, Quebec, Canada.Nanocrystalline cellulose is typically about 100 nm to
200 nm long and is typically about 5 nm to 10 nm in diameter. During manufacture,
cellulose is milled and hydrolyzed to remove amorphous regions. The resulting nanocrystalline
cellulose is then separated and concentrated before being modified for coating applications.
Nanocrystalline cellulose is light weight, biodegradable, non-toxic, cost-efficient,
and recyclable.
[0023] Suitable nanoclay materials (vi) include platey kaolins, nanoclays, clay nanocomposite,
and polymer-clay nanocomposite structures including hyper-platey, nano-dimensional
thickness crystals. Nanoclay materials as described herein can be e.g. dispersed within
a polymer-based or water-based matrix.
[0024] Suitable inorganic oxide materials (vii) that perform as a barrier layer or coating
include aluminum oxide (AlOx), silicon oxide (SiOx), and magnesium oxide (MgOx). In
the aforementioned oxide materials, "x" is a suitable number or fraction for the stoichiometric
amount of oxygen (e.g., Al
2O
3, SiO
2, MgO). Such oxide coatings may be prepared using plasma-assisted deposition on a
substrate.
[0025] The thickness of the cardboard (laminate) including the (preferably corrugated) cardboard
and the optional vapor/moisture barrier layer preferably should be in the range from
0,5 mm to 3 mm to provide suitable stability to said container, more preferred 0,8
mm to 2,5 mm, even more preferred 1 mm to 2 mm.
[0026] According to the invention the cardboard container comprises a top surface (1), a
bottom (2) and at least three, preferably at least four side surfaces (3) and a closure
(4) slidely movable between a position closing the container and a position providing
an opening (O), see FIG. 1 and Fig. 2.
[0027] Preferably the cardboard container comprises a main container body which is preferably
folded from one continuous piece of a cardboard panel, cut in a form allowing the
folding into the container main body of the present invention. Said container main
body has at least three, preferably four side surfaces (3) an upper surface (11) and
a bottom (2). In a particularly preferred embodiment said upper surface (11) comprises
a perforation or pre-cut for an opening (O1), which can be removed by pushing it so
that opening (O1) is obtained. In FIG. 3a an embodiment is shown wherein said container
main body has only one flap representing upper surface (11). The main body may have
two overlapping flaps (11a, 11b) providing together surface (11), wherein one of it
(11a) has said perforation or pre-cut for said opening (O1) and the other one (11b)
has a punched hole (12) corresponding in size and position to openings (O) and (O1)
(FIG. 3b), or is shorter in length (FIG 4a) or width (FIG. 4b), so that the area below
the perforation or pre-cut for said opening (O1) is kept free from container material.
Said perforation or pre-cut for opening (O1) serves as a proof for non-use of the
package, thus, the consumer can be sure that the package comprises all of and only
those items originally filled in by the producer.
[0028] In another embodiment said main body of the container comprises only one flap representing
an upper surface (11) which is not fully spanning the length of the container, so
that the area below punched hole (8) / opening (O) of the top surface (1) is free
of cardboard material. In still another embodiment said main body of the container
comprises an upper surface (11) which is not fully spanning the width of the container,
so that the area below punched hole (8) / opening (O) of the top surface (1) is free
of cardboard material, e.g. surface (11) is provided by two small flaps supporting
the closure (4) / top surface (1), however, leaving the area below punched hole (8)
/ opening (O) free of cardboard material. In these embodiments a "non-use proof" may
be realized e.g. by applying a paper strip on top surface (1) spanning at least embossment
(6) and punched hole (8).
[0029] The cardboard container further comprises a top surface (1) having at least two punched
holes (8, 9) and further preferably a passage (10) allowing a terminal end (E) of
the flat panel (5) of closure (4) to move through said passage (10) in an outward
direction to allow movement of the closure (4) (FIG, 5). In a preferred embodiment
the punched holes (8, 9) are lying "in-line" in a direction of movement of closure
(4), i.e. both punched holes (8, 9) are positioned in the plane area of top surface
(1), not on the edges.
[0030] As a further component the cardboard container comprises a closure (4), comprising
a flat panel (5) having on one surface at least two embossments (6, 7) which are shaped
in a form so that they fit into the punched holes (8, 9) of the top surface (1) to
close the container. Further said flat panel (5) has a front end (F) which is close
to embossment (6) and an opposing terminal end (E), which is the end farest away from
embossment (6), Said closure is mounted slidably movable below said top surface (1),
or "sandwiched" between the upper surface (11) of the main body and top surface (1)
in an orientation so that in the "closed " position the embossments (6, 7) fill the
punched holes (8, 9). Between the front end (F) and terminal end (E) the flat panel
(5) preferably includes a stop element (S), e.g. a shoulder, avoiding that said closure
(4) is moved / pulled out too far from the container. A suitable embodiment of such
a closure (4) is shown in FIG. 6 and FIG. 7.
[0031] The top surface (1) may be an integral part of the continuous panel cut in form of
the container main body, however, preferably is an independent panel cut in a suitable
shape to fit on top of the container main body and to be fastened in its position.
Said top surface panel is preferably applied to the main body in a distance allowing
to "sandwich" the closure (4) between surface (11) of the main body and said top surface
(1), so that closure (4) after pushing the embossments (6, 7) is slidely movable between
said surfaces. In a preferred embodiment at least one of the side surfaces (3) provides
at the edge between the upper surface (11) and said side surface (3) at least one
suitable small bulge (B) ensuring said distance between said upper surface (11) and
said top surface (1) when it is placed and combined with said container main body
by means of an adhesive, fixing material or fixing device.
[0032] It is possible that all parts of the container of the present invention, i.e. said
main body, said independent top surface (1) and said closure (4), are made from the
same cardboard material. It is, however, also possible to prepare the main body of
the container from a cardboard material comprising said moisture barrier, wherein
said independent top surface (1) and/or said closure (4) are made of a cardboard panel
(having preferably similar thickness and construction), having no moisture barrier
included. Due to environment protection and cost advantages the last embodiment might
be preferred.
[0033] In all described embodiments of the cardboard container punched hole (8) is closed
by embossment (6) when the closure (4) is fully inserted into the container, thus
lying with its full length directly below surface (1), or between surface (1) and
surface (11). This is described as the "closed" position. If the closure (4) is moved
laterally in an outward direction, so that its terminal end (E) leaves the container,
e.g. by passing through passage (10), said punched hole (8) represents opening (O),
which allows the removal, discharge, pouring or taking out of the content comprised
in said container. Indeed, it is to be understood that opening (O1) or the perforation
/ precut for opening (O1) is placed in accordance with opening (O), thus, any content
removed, discharged, poured or taken out from the container is passing both openings
placed at the similar position. The position where embossment (6) of closure (4) is
not engaging with punched hole (8), but leaves said hole open to provide opening (O),
is defined as the "open" position.
[0034] A similar construction as what is described above as being realized at the "top surface
(1)" also can be positioned accordingly at any of the "side surfaces (3)", meaning
that the closure (4) is not placed on top of the container, but at one of the side
surfaces, however, has the equivalent construction.
[0035] With "top surface" a surface is meant being at the uppermost end of the container
when said container is placed (stored) as usual for using it. With "side surface"
a surface is meant which is positioned either in front, in back, on the left or on
the right side, when the package / container is placed (e.g. for storage) on a surface.
[0036] It is preferred according to the invention that the punched holes (8, 9) are spaced
apart from each other by a distance (D) of at least 1 cm, preferably at least 1,5
cm, more preferred at least 2 cm, even more preferred at least 2,5 cm, said distance
(D) is measured from one border of punched hole (8) to the closest boarder of punched
hole (9). Accordingly, embossments (6, 7) are also spaced apart from each other by
distance (D).
[0037] Further, punched hole (8), providing opening (O) in the "open" position of closure
(4), has a form and diameter suitably adapted to the size and or form of the content
of the package container. The form and diameter of punched hole (8) / opening (O)
can be selected either to allow the content, e.g. a shaped item, to fall out unhindered,
if the container is turned accordingly, or it might be selected in a way allowing
the shaped item to enter opening (O), but not to fall out without some help by the
consumer. If, for example, the shaped item is a pouch having several compartments
comprising liquid and/or powdery composition(s), the punched hole (8) / opening (O)
can be formed in a shape so that said pouch has to be turned and/or compressed a little
bit to get it out of the opening. This can be a further hurdle for children to have
access to the container content.
[0038] Nonetheless, the diameter at the smallest site of punched hole (8) / opening (O)
preferably is at least 2 cm, more preferred at least 2,5 cm, even more preferred at
least 3 cm, even more preferred at least 3,5 cm or even at least 4 cm or at least
5 cm, in particular if the content of the container is/are shaped item/s). It is,
however, preferred according to the invention that punched hole (8) / opening (O)
leaves a remainder of the cardboard material between the border of the hole (8) and
the edge of top surface (1), said remainder may be represented by at least 0,3 cm,
at least 0,5 cm, at least 0,8 cm, at least 1 cm, or at least 1,5 cm of cardboard material
between the border of the hole and the edge of top surface (1).
[0039] The second punched hole (9) may have any form and size allowing to provide pressure
on the engaging embossment (7) with at least one finder of a human hand, e.g. 2 to
4 cm at its smallest site.
[0040] It is preferred that punched hole (8) and embossment (6), or punched hole (9) and
embossment (7) independently from each other have a form which can be easily cut by
punching tools, thus, a circular, rectangular (optional with rounded corners), square
(optional with rounded corners), oval, elliptic or any combination of these forms
are preferred. Of course, the form of embossment (6) fits to punched hole (8) and
the form of embossment (7) fits to punched hole (9).
[0041] It is particularly preferred that both punched holes (8, 9) are provided in the flat
area of top surface (1) leaving a remainder of the cardboard material between the
hole and the edge of top surface (1). This means that preferably both punched holes
(8, 9) are not positioned at the edge of said surface (1).
[0042] The container can be opened by a consumer by applying simultaneously pressure to
both embossments (6, 7) engaging into punched holes (8, 9) in the "closed" position,
and by lateral movement of the closure (4) to one side. If the full length of the
closure (4) is similar to the length of the top surface (4), one edge between top
surface (4) and one side surface (3) preferably should provide a passage (10) allowing
the terminal end (E) of the flat panel (5) to leave the container. The terminal end
(E) of flat panel (5) protruding from the container when embossments (6, 7) are pressed
down and closure (4) is moved laterally can further be used to pull the closure further
out to open said opening (O) fully.
[0043] To stop the movement of the closure, thus, to avoid that said closure (4) is moved
out too far, said closure preferably comprise a shoulder serving as a stop (S).
[0044] If desired, the container may comprise in at least one, preferably in at least two
of its bottom flaps positioned at the inner side of the container (2a, 2c, as exemplified
in FIG. 8) forming said bottom (2) punched holes (13) having any suitable size and
form, which (i) don't destabilize said flap (2a or 2c) or bottom (2), (ii) allow to
fix said flap (2a) / (2c) to at least one of the other bottom flaps (2b, 2d) and (iii)
to provide some space for collecting optionally some fluid or liquid tickling out
from any liquid-filled content, e.g. liquid-filled detergent pouches, comprised in
the container of the invention. Preferably said punched holes (13) each have a length
of 50% to 85%, preferably 60% to 80% of the length of the respective flap comprising
said hole (13), and a width of 5 to 15% of the width of the respective flap.
FIGURES
[0045] The figures show illustrative embodiments of the container of the present invention,
without restricting the invention exactly to what is shown. In all the figures thick
lines refers to cut edges, dash-dotted lines _._._._. refer to a perforation or pre-cut.
Thin lines are folding lines (L).
FIG. 1 shows a cuboid container having the closure (4) on the top surface (1) in "closed"
position.
FIG. 2 shows the cuboid container of FIG. 1 having the closure (4) in an "open" position.
FIG. 3 shows a cardboard panel cut in a form for folding a container main body according
to the embodiment providing a surface (11). In FIG. 3a said surface (11) is provided
only by one flap, in FIG. 3b said surface (11) is provided by two flaps (11a, 11b),
overlapping in the folded container.
FIG. 4 shows a cardboard panel cut in a form for folding a container main body according
to the embodiment wherein surface (11b) is not spanning the whole length of the container
(FIG. 4a), or not spanning the whole width of the container (FIG. 4b).
Fig. 5 shows a cardboard panel cut in a form for providing a top surface (1) as a
separate component to be mounted on top of a container main body as shown in FIG.
3 or FIG. 4.
FIG. 6 shows one embodiment of a closure (4) as a separate component as a top view.
FIG. 7 shows the closure (4) as an inclined top view.
FIG. 8 shows an embodiment of a cardboard panel cut in form of the container main
body, having punched holes (13) in the bottom flaps (2a, 2c) serving for collecting
optionally liquid inside the container.
CONTENT OF THE CONTAINER
[0046] According to the invention the package container comprises shaped or granular item(s),
selected from (a) detergent or cleaning agents or (b) water softeners.
[0047] With "shaped item" is meant that the composition is provided in form of a body, e.g.
a tablet, capsule, sphere, pellets, beads, or as a pouch or sachet comprising a packaging
film and a liquid, gelly, pasty or solid (e.g. in form of a powder, particles, granulate,
pressed or sintered) detergent or cleaning composition. Said pouch or sachet can be
provided with one compartment or with more than one compartment, wherein each of the
compartments independent from each other can comprise a composition in a form as defined
above. Thus, said pouch or sachet can comprise e.g. only liquid composition(s) (optionally
differing from each other in their ingredients), a combination of liquid composition(s)
and solid composition(s), a combination of liquid and gelly composition(s) or a combination
of gelly and solid composition(s), or even a combination of liquid, gelly and solid
composition(s) in different compartments. Further, a tablet, capsule, sphere, pellet
or bead may also comprise different layers or areas, providing optionally different
ingredients, e.g. a multi-layer body, a tablet having a mould filled with a solid,
gelly or pasty composition or any of the embodiments known in the art commonly used
for providing such detergent / cleaning compositions in form of shaped bodies.
[0048] Further, the content of the package container may be in "granulate form", that means
that the composition can be provided as particles having a particle size in the range
of from 0,1 mm to 2 mm, e.g. 0,2 to 1,5 mm, but having an "irregular shape", which
means that not all the granules have the same size or shape.
DETERGENT OR CLEANING COMPOSITION (a)
[0049] The detergent or cleaning composition of the present invention is preferably a laundry
cleaning composition or a dishwashing composition, more preferably a laundry or an
automatic dishwashing composition. The cleaning composition can be provided in form
a pouch comprising a liquid, a gel, a paste a, powder, granulates, particles, including
pouches with different compartments comprising combinations of the mentioned, or as
a mono-layer tablet, a multi-layer or multiphase (e.g. tab in tab) tablet, a bar or
any other suitable form or combinations thereof. Particularly preferred the cleaning
composition is provided in form of a pouch or a sachet comprising said composition
in form a liquid, a gel, a paste a, powder, granulates, particles or combinations
thereof or in form of a tablet, a sphere, a pressed, sintered or shaped body or in
granulate form.
[0050] If the detergent or cleaning composition is provided in form of a pouch or sachet,
it might be provided as a pouch having one compartment, two compartments, three compartments
or four compartments, or even having more than four compartments, e.g. five, six,
seven or more compartments, without any restriction. It is, however, preferred that
said pouch or sachet comprises one to four, preferably two, three or four compartments.
[0051] Such type of pouches or sachets are known in the art and commonly are prepared by
usage of a water-soluble film material, forming the compartment(s) which is/are filled
with detergent compositions in liquid, gelly or solid (e.g. particulate, powder or
granular) form. The compartments may comprise compositions having differing ingredients,
providing together the "whole" detergent composition. Examples of suitable ingredients
of the detergent composition are described below.
[0052] Suitable water-soluble film materials for forming the pouches are well known in the
art and include commonly polyvinylalcohol polymer or a polyvinylalcohol copolymer.
[0053] The preferred material for making the pouch or sachet comprises water-soluble polyvinyl
alcohol (including co-polymers thereof), wherein preferably the polymer present in
the film is from 60 to 100%, more preferably 80% to 98%, and most preferably 80% to
95% hydrolysed, to improve the dissolution of the material.
[0054] Suitable co-polymers include monomers of carboxylates, sulphonates and ethoxylates.
Itaconic acid, acrylic acid, methacrylic acid are examples of suitable carboxylic
acid, 2-acrylamido-2-methyl-1-propane sulphonic acid (AMPS) is an example of a preferred
sulphonic acid.
[0055] The water-soluble film herein may comprise furter additive ingredients. For example,
it may be beneficial to add plasticisers, for example glycerol, ethylene glycol, diethyleneglycol,
propylene glycol, propane diol, sorbitol and mixtures thereof, additional water, disintegrating
aids, fillers, anti-foaming agents, emulsifying/dispersing agents, and/or antiblocking
agents. It may be useful that the pouch or water-soluble film itself comprises a detergent
additive to be delivered to the wash water, for example organic polymeric soil release
agents, dispersants or dye transfer inhibitors. Optionally the surface of the film
of the pouch may be dusted with fine powder to reduce the coefficient of friction.
Sodium aluminosilicate, silica, talc and amylose are examples of suitable fine powders.
[0056] Highly preferred for preparation of the pouches / sachets are polyvinyl alcohol films
formed by extrusion, blow-extrusion, blow-molding, extrusion casting or solution casting
into a thin film. Such a film is preferably 10 to 200 micrometers thick, more preferably
from 40 to 100 micrometers thick. Particularly suitable commercially available films
are provided under the tradename MonoSol® by MonoSol (Kuraray) company.
[0057] The cleaning composition(s) of the present invention may comprise any of the ingredients
known in the art as common ingredients in cleaning compositions, particularly in laundry
or automatic dishwashing compositions. Such ingredients are selected from the group
consisting of e.g. builders, surfactants, preferably non-ionic and/or anionic surfactants,
polymers/cobuilders, enzymes, complexing agents, bleaching agents, dispersing agents,
optical brighteners, stabilizers, colorants, odorants, anti-redeposition agents, anti-corrosion
agents, tableting agents, desintegrants, silver protecting agents, dyes, and perfume,
without any restriction.
[0058] According to the invention the cleaning composition comprises preferably at least
one type of a surfactant, preferably non-ionic and/or anionic surfactants, and an
alkaline or acid compound and further preferably at least one type of a builder and/or
at least one enzyme.
[0059] Furthermore, all of the optional ingredients known in the state of the art to be
effective or usable in cleaning compositions, particular in laundry or in automatic
dishwashing compositions might be included. Said further ingredients are not limiting
the present invention.
[0060] The following ingredients represent examples of ingredients which can be included
in a cleaning composition of the present invention, however should not be considered
as limited to the mentioned.
Surfactants
[0061] The cleaning composition of the present invention comprises one or more surfactants.
Said surfactants may be selected from anionic, non-ionic, cationic or amphoteric surfactants,
however, are preferably anionic and/or non-ionic.
[0062] The main functions of surfactants are changing the surface tension, dispersing, foam
controlling and surface modification.
[0063] Examples of possible surfactant as at least one ingredient can be selected from the
group consisting of anionic, cationic, non-ionic as well as amphoteric surfactants,
and preferably may be selected from the group consisting of anionic or non-ionic surfactants
or mixtures thereof. More preferably, the composition of the present invention comprises
a mixture of anionic and non-ionic surfactants. If surfactants are present in the
composition of the present invention, their total amount preferably may be in the
range of from 0,1 to 50 wt.-%, more preferably of from 1 to 30 wt.-%, even more preferably
of from 1,5 to 25 wt.-%, even more preferably of from 1,5 to 20 wt.-%, and most preferably
of from 1,5 to 15 wt.-%, based on the whole composition. Preferably the composition
comprises at least one nonionic surfactant and optionally at least one anionic surfactant.
[0064] Anionic surfactants suitable to be used in cleaning compositions, in particular in
combination with enzymes are well known in the state of the art and include for example
alkylbenzenesulfonic acids or salts thereof and alkylsulfonic acids or salts thereof.
[0065] Suitable anionic alkylbenzene sulfonic or alkylsulfonic surfactants include in particular
C
5-C
20, preferably C
10-C
16, even more preferably C
11-C
13 alkylbenzenesulfonates, in particular linear alkylbenzene sulfonates (LAS), alkylestersulfonates,
primary or secondary alkenesulfonates, sulfonated polycarboxylic acids and any mixtures
thereof. Alkylethersulfates may be used as well.
[0066] Further preferred surfactants are non-ionic, in particular low foaming non-ionic
surfactants. Washing or cleaning agents, particularly laundry cleaning agents or dishwashing
and among this preferably automatic dishwashing compositions, are especially preferred
when they comprise non-ionic surfactants from the group of the alkoxylated alcohols.
Preferred non-ionic surfactants are alkoxylated, advantageously ethoxylated, particularly
primary alcohols preferably containing 8 to 18 carbon atoms and, on average, 1 to
12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol group may
be linear or, preferably, methyl-branched in the 2-position or may contain e.g. linear
and methyl-branched residues in the form of the mixtures typically present in Oxo
alcohol residues. Particularly preferred are, however, alcohol ethoxylates with linear
groups from alcohols of natural origin with 6 to 22 carbon atoms, e.g. from coco-,
palm-, tallow- or oleyl alcohol, and an average of 2 to 8 EO per mole alcohol. Exemplary
preferred ethoxylated alcohols include C
12-14 alcohols with 3 EO or 4 EO, C
9-11 alcohols with 7 EO, C
13-15 alcohols with 3 EO, 5 EO or 7 EO, C
12-18 alcohols with 3 EO, 5 EO or 7 EO and mixtures thereof, such as mixtures of C
12-14 alcohols with 3 EO and C
12-18 alcohols with 5 EO. The cited degrees of ethoxylation constitute statistically average
values that can be a whole or a fractional number for a specific product. Preferred
alcohol ethoxylates have a narrowed homolog distribution (narrow range ethoxylates,
NRE). In addition to these non-ionic surfactants, fatty alcohols with more than 12
EO can also be used. Examples of these are tallow fatty alcohol with 14 EO, 25 EO,
30 EO or 100 EO.
[0067] Accordingly, ethoxylated non-ionic surfactant(s) prepared from C
6-20 monohydroxy alkanols or C
6-20alkylphenols or C
12-20 fatty alcohols and more than 12 mole, preferably more than 12 mole and especially
more than 20 mole ethylene oxide per mole alcohol, are used with particular preference.
A particularly preferred non-ionic surfactant is obtained from a straight-chain fatty
alcohol containing 16 to 20 carbon atoms (C
16-20 alcohol), preferably a C
18 alcohol, and at least 12 moles, preferably at least 15 moles and more preferably
at least 20 moles of ethylene oxide. Of these non-ionic surfactants, the so-called
narrow range ethoxylates are particularly preferred.
[0068] Moreover, surfactant(s) that comprise one or more tallow fat alcohols with 20 to
30 EO may be used in combination with a silicone defoamer.
[0069] A special type of surfactants used in automatic dishwasher cleaning compositions
is a 'carry-over' surfactant. A 'carry-over' surfactant has the property that some
amount of the surfactant used remains in the machine after the rinsing cycles to give
a performance during the final rinsing cycle and the (optional) drying phase of the
whole washing cycle of the dishwashing machine. This type of surfactant is described
in
EP 1 524 313 in more detail.
[0070] Further, for cleaning compositions alkoxylated nonionic surfactants and Gemini surfactants
are commonly used. The alkoxy groups mostly consist of ethyleneoxide, propyleneoxide
and butyleneoxide or combinations thereof. Also, amphoteric surfactants are known
to be used in cleaning compositions. Further, alkylpolyglucoside surfactants can also
be used, preferably in a low foaming form.
[0071] Examples of further surfactants are selected from a group consisting of gemini surfactants
with a short C-Chain (C8-C12) as spacer and two times 5-40EO groups as hydrophilic
headgroups (e.g. Dehypon GRA, Dehypon E 127, Genapol EC 50, Genapol EC 65) and Long
Chain (C12-22) high ethoxylateted (20-100EO) carry over surfactant Lutensol AT Types.
[0072] Further, all surfactants commonly known to be used in cleaning compositions can be
part of the composition, this includes all anionic, non-ionic, cationic and amphoteric
surfactants known in the art. The present invention is not limited by any of the surfactants
commonly used in cleaning compositions.
Builder(s), Co-Builder(s)
[0073] The composition of the present invention preferably comprises one or more builder(s).
[0074] The main functions of the builders are to soften the washing water, to provide alkalinity
and a buffering capacity to the washing liquid and to have an anti-redeposition or
dispersing function in the cleaning composition. The physical properties of the cleaning
composition are also depending on the builders that are used.
[0075] For controlling the pH of the composition, as well as its mineral hardness, inorganic
as well as organic builders may be incorporated into the composition. In addition,
these builders may assist in the removal of particulate soil. If present in the composition
according to the present invention, the builder or the mixture of builders preferably
will be present in an amount of from 0,1 to 90 wt.-%, preferably in an amount of from
5 - 80 wt.-%, more preferably in an amount of 8 - 70 wt.-%, and even more preferably
in an amount of from 10 - 50 wt.-%, based on the whole composition.
[0076] Included among the builders in this context are, in particular, the silicates, aluminosilicates,
carbonates, sulfates, organic co-builders, and - in cases where no environmental prejudices
against their use exist - also the phosphates, which, however, are not preferred.
Phosphate builders include alkaline, ammonium or alkanolammonium salts of polyphosphates,
including tripolyphosphates, pyrophosphates and polymeric metaphosphates. In one embodiment,
the composition of the present invention comprises less than 5 wt.-% of a polyphosphate
builder, based on the whole composition.
[0077] Among the plurality of commercially obtainable phosphates, the alkali metal phosphates
have the highest importance for the agents according to the present invention, with
particular preference for pentasodium triphosphate, Na
5P
3O
10 (sodium tripolyphosphate) resp. pentapotassium triphosphate, K
5P
3O
10 (potassium tripolyphosphate).
[0078] If phosphates are used, the weight proportion of the phosphate in terms of the total
weight of the cleaning composition is preferably from 1 to 70 wt.-%, more preferably
from 10 to 60 wt.-%, and most preferred from 20 to 50 wt.-%.
[0079] In addition to or instead of an inorganic builder the composition of the present
invention may as well comprise an organic builder, including polycarboxylate builders
in the form of their acid or a salt, including alkali metal salts such as potassium,
sodium and lithium salts.
[0080] The group of preferred builders includes in particular the citrates as well as the
carbonates and the organic co-builders. The term "citrate" hereby includes both citric
acid as well as its salts, in particular its alkali metal salts. These builders are
acid or alkaline and thus further can be used for adapting the pH of the composition.
[0081] Carbonate(s) and/or hydrogen carbonate(s), preferably alkali metal carbonate(s),
particularly preferably sodium carbonate or bicarbonate, are particularly preferably
added in quantities of 5 to 70 wt.-%, preferably 10 to 40 wt.-% and especially 15
to 60 wt.-%, each relative to the weight of the detergent composition.
[0082] Polycarboxylates/polycarboxylic acids and phosphonates may be particularly mentioned
as the organic co-builders. These classes of substances are described below.
[0083] Useful organic builders are, for example, the polycarboxylic acids that can be used
in the form of the free acid and/or their sodium salts, polycarboxylic acids in this
context being understood to be carboxylic acids that carry more than one acid function.
These include, for example, adipic acid, succinic acid, glutaric acid, malic acid,
tartaric acid, maleic acid, fumaric acid, sugar acids, amino carboxylic acids, nitrilotriacetic
acid (NTA) and mixtures thereof. Besides their building effect, the free acids also
typically have the property of an acidifying component and hence also serve to establish
a relatively low and mild pH of the inventive agents. Succinic acid, glutaric acid,
adipic acid, gluconic acid and any mixtures thereof are particularly to be mentioned
in this regard.
[0084] Usable organic builder substances are, for example, the polycarboxylic acids usable
in the form of the free acid and/or sodium salts thereof, "polycarboxylic acids" being
understood as those carboxylic acids that carry more than one acid function. These
are, for example, citric acid, adipic acid, succinic acid, glutaric acid, malic acid,
tartaric acid, maleic acid, fumaric acid, sugar acids, aminocarboxylic acids, nitrilotriacetic
acid (NTA), provided such use is not objectionable for environmental reasons, as well
as mixtures thereof. The free acids typically also possess, besides their builder
effect, the property of an acidifying component, and thus also serve to establish
a lower and milder pH for washing or cleaning agents. To be recited in this context
are, in particular, citric acid, succinic acid, glutaric acid, adipic acid, gluconic
acid, and any mixtures thereof.
[0085] Citric acid or salts of citric acid are used with particular preference as a builder
substance.
[0086] A further particularly preferred builder substance is methylglycinediacetic acid
(MGDA). According to the invention it is particularly preferred to add MGDA as at
least one builder / complexing agent into the composition.
[0087] Oxydisuccinates and other derivatives of disuccinates, preferably ethylenediamine
disuccinate, are additional suitable co-builders. Ethylenediamine-N,N'-disuccinate
(EDDS might be used, preferably in the form of its sodium or magnesium salts. Also
preferred in this context are glycerol disuccinates and glycerol trisuccinates.
[0088] In order to improve cleaning performance and/or to adjust viscosity, liquid cleaning
agents may contain at least one hydrophobically modified polymer, preferably a hydrophobically
modified polymer containing carboxylic acid groups, the weight amount of the hydrophobically
modified polymer in terms of the total weight of the cleaning agent being preferably
0,1 to 10 wt.-%, preferably between 0,2 and 8,0 wt.-%, and in particular 0,4 to 6,0
wt.-%.
Polymers
[0089] Supplementing the builders described above, polymers having cleaning activity can
be contained in the cleaning agent. The weight proportion of the polymers having cleaning
activity in terms of the total weight of automatic cleaning agents according to the
present invention is preferably from 0,1 to 20 wt.-%, preferably 1,0 to 15 wt.-%,
and in particular 2,0 to 12 wt.-%.
[0090] Suitable polymers are known to those skilled in the art and comprise e.g. polymeric
polycarboxylates; these are, for example, the alkali metal salts of polyacrylic acid
or of polymethacrylic acid, for example those having a relative molecular weight from
500 to 70.000 g/mol or derivatives thereof.
[0091] The molecular weight indicated for polymeric polycarboxylates are herein weight-average
molecular weights Mw of the respective acid form that were determined in principle
by means of gel permeation chromatography (GPC), a UV detector having been used. The
measurement was performed against an external polyacrylic acid standard that yields
realistic molecular weight values because of its structural affinity with the polymers
being investigated.
[0092] Suitable polymers are, in particular, polyacrylates that preferably have a molecular
weight from 2.000 to 20.000 g/mol. Of this group in turn, the short-chain polyacrylates,
which have molecular weights from 2.000 to 10.000 g/mol and particularly preferably
from 3.000 to 5.000 g/mol, may be preferred because of their superior solubility.
[0093] Also suitable are copolymeric polycarboxylates, in particular those of acrylic acid
with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid. Copolymers
of acrylic acid with maleic acid that contain 50 to 90 wt.-% acrylic acid and 50 to
10 wt.-% maleic acid have been found particularly suitable. Their relative molecular
weight, based on free acids, is equal to in general 2.000 to 70.000 g/mol, preferably
20.000 to 50.000 g/mol, and in particular 30.000 to 40.000 g/mol.
[0094] Sulfonic acid group-containing polymers, in particular those from the group of the
copolymeric polysulfonates, are used preferably as polymers having cleaning activity.
These copolymeric polysulfonates contain, besides sulfonic acid group-containing monomer(s),
at least one monomer from the group of the unsaturated carboxylic acids.
[0095] As monomers of said copolymers unsaturated carboxylic acids of the formula R
1(R
2)C=C(R
3)COOH are used with particular preference as (an) unsaturated carboxylic acids(s),
in which formula R
1 to R
3, mutually independently, denote -H, -CH
3, a straight-chain or branched saturated alkyl residue having 2 to 12 carbon atoms,
a straight-chain or branched, mono- or polyunsaturated alkenyl residue having 2 to
12 carbon atoms, alkyl or alkenyl residues as defined above substituted with -NH
2, -OH, or -COOH, or denote -COOH or -COOR
4 where R
4 is a saturated or unsaturated, straight-chain or branched hydrocarbon residue having
1 to 12 carbon atoms.
[0096] Particularly preferred unsaturated carboxylic acids are acrylic acid, methacrylic
acid, ethacrylic acid, α-chloroacrylic acid, α-cyanoacrylic acid, crotonic acid, α-phenylacrylic
acid, maleic acid, maleic acid anhydride, fumaric acid, itaconic acid, citraconic
acid, methylenemalonic acid, sorbic acid, cinnamic acid, or mixtures thereof. The
unsaturated dicarboxylic acids are of course also usable.
[0097] In the context of the sulfonic acid group-containing monomers, those of the formula
R
5(R
6)C=C(R
7)-X-SO
3H, in which R
5 to R
7, mutually independently, denote -H, -CH
3, a straight-chain or branched saturated alkyl residue having 2 to 12 carbon atoms,
a straight-chain or branched, mono- or polyunsaturated alkenyl residue having 2 to
12 carbon atoms, alkyl or alkenyl residues substituted with -NH
2, -OH, or -COOH, or denote -COOH or -COOR
4, where R
4 is a saturated or unsaturated, straight-chain or branched hydrocarbon residue having
1 to 12 carbon atoms, and X denotes an optionally present spacer group that is selected
from-(CH
2)
n- where n=0 to 4, -COO-(CH
2)
k- where k=1 to 6, -C(O)-NH-C(CH
3)
2-, -C(O)-NH-C(CH
3)
2-CH
2-, and -C(O)-NH-CH(CH
2CH
3)-, are preferred.
[0098] Among these monomers, those of the formula
H
2C=CH-X-SO
3H
H
2C=C(CH
3)-X-SO
3H
HO
3S-X-(R
6)C=C(R
7)-X-SO
3-H,
in which R
6 and R
7, mutually independently, are selected from -H, -CH
3, -CH
2CH
3, -CH
2CH
2CH
3, -CH(CH
3)
2, and X denotes an optionally present spacer group that is selected from -(CH
2)
n- where n=0 to 4, -COO-(CH
2)
k- where k=1 to 6, -C(O)-NH-C(CH
3)
2-, -C(O)-NH-C(CH
3)
2-CH
2-, and -C(O)-NH-CH(CH
2CH
3)-, are preferred.
[0099] Particularly preferred sulfonic acid group-containing monomers in this context are
1-acryiamido-1-propanesuifonic acid, 2-acrylamido-2-propanesulfonic acid, 2-acrylamido-2-methyl-1-propanesulfonic
acid, 2-methacrylamido-2-methyl-1-propanesulfonic acid, 3-methacrylamido-2-hydroxypropanesulfonic
acid, allylsulfonic acid, methallylsulfonic acid, allyloxybenzenesulfonic acid, methallyloxybenzenesulfonic
acid, 2-hydroxy-3-(2-propenyloxy)propanesulfonic acid, 2-methyl-2-propene-1-sulfonic
acid, styrenesulfonic acid, vinylsulfonic acid, 3-sulfopropylacrylate, 3-sulfopropylmethacrylate,
sulfomethacrylamide, sulfomethylmethacrylamide, and mixtures of the aforesaid acids
or water-soluble salts thereof.
[0100] The copolymers can also encompass, besides carboxyl group-containing monomers and
sulfonic acid group-containing monomers, at least one nonionic, preferably hydrophobic
monomer. The use of these hydrophobically modified polymers allows to improve, in
particular, the rinsing performance of automatic dishwashing agents.
[0101] Cleaning agents containing a copolymer encompassing
- i) carboxylic acid group-containing monomer(s),
- ii) sulfonic acid group-containing monomer(s),
- iii) optionally (a) nonionic monomer(s), are preferred according to the present invention.
[0102] The use of these terpolymers has made it possible to improve the rinsing performance
of automatic dishwashing agents with respect to comparable dishwashing agents that
contain sulfopolymers without the addition of nonionic monomers.
[0103] The nonionic monomers used are preferably monomers of the general formula R
1(R
2)C=C(R
3)-X-R
4, in which R
1 to R
3, mutually independently, denote -H, -CH
3, or -C
2H
5, X denotes an optionally present spacer group that is selected from -CH
2-, -C(O)O-, and -C(O)-NH-, and R
4 denotes a straight-chain or branched saturated alkyl residue having 2 to 22 carbon
atoms or an unsaturated, preferably aromatic residue having 6 to 22 carbon atoms.
[0104] Particularly preferred nonionic monomers are butene, isobutene, pentene, 3-methylbutene,
2-methylbutene, cyclopentene, hexene, hexene-1, 2-methlypentene-1, 3-methlypentene-1,
cyclohexene, methylcyclopentene, cycloheptene, methylcyclohexene, 2,4,4-trimethylpentene-1,
2,4,4-trimethylpentene-2, 2,3 -dimethylhexene-1,2,4-dimethylhexene-1, 2,5-dimethlyhexene-1,
3,5-dimethylhexene-1, 4,4-dimethylhexane-1, ethylcyclohexyne, 1-octene, α-olefins
having 10 or more carbon atoms such as, for example, 1-decene, 1-dodecene, 1-hexadecene,
1-octadecene, and C22-α-olefin, 2-styrene, α-methylstyrene, 3-methylstyrene, 4-propylstryene,
4-cyclohexylstyrene, 4-dodecylstyrene, 2-ethyl-4-benzylstyrene, 1-vinylnaphthalene,
2-vinylnaphthalene, acrylic acid methyl ester, acrylic acid ethyl ester, acrylic acid
propyl ester, acrylic acid butyl ester, acrylic acid pentyl ester, acrylic acid hexyl
ester, methacrylic acid methyl ester, N-(methyl)acrylamide, acrylic acid 2-ethylhexyl
ester, methacrylic acid 2-ethylhexyl ester, N-(2-ethylhexyl)acrylamide, acrylic acid
octyl ester, methacrylic acid octyl ester, N-(octyl)acrylamide, acrylic acid lauryl
ester, methacrylic acid lauryl ester, N-(lauryl)acrylamide, acrylic acid stearyl ester,
methacrylic acid stearyl ester, N-(stearyl)acrylamide, acrylic acid behenyl ester,
methacrylic acid behenyl ester, and N-(behenyl)acrylamide, or mixtures thereof.
[0105] The weight proportion of the sulfonic acid group-containing copolymers in terms of
the total weight of cleaning agents according to the present invention is preferably
from 0,1 to 15 wt.-%, preferably from 1,0 to 12 wt.-%, and in particular from 2,0
to 10 wt.-%.
[0106] Organic co-builders that may be recited are in particular polycarboxylates/polycarboxylic
acids, polymeric polycarboxylates, aspartic acid, polyacetals, dextrins or further
organic co-builders.
Enzymes
[0107] The composition of the present invention further comprises at least one enzyme.
[0108] In general, enzymes are often used to aid the removal of stains. In most cases enzymes
react with the soiling and break it down into pieces that have increased water solubility
or are better dispersible in the washing liquid.
[0109] The enzymes that can be used in cleaning compositions include, but are not limited
to, proteases, amylases, lipases, cellulases, mannanase, peroxidase, oxidase, xylanase,
pullulanase, glucanase, pectinase, cutinase, hemicellulases, glucoamylases, phospholipases,
esterases, keratanases, reductases, phenoloxidases, lipoxygenases, ligninases, tannases,
pentosanases, malanases, arabinosidases, hyaluronidase, chondroitinase, laccase or
mixtures thereof. These enzymes are known to the skilled artisans.
[0110] Particularly preferred enzymes are selected from a group consisting of amylases,
lipases, proteases, cellulases or mixtures thereof, most preferred at least one enzyme
is a protease.
[0111] Each of said enzymes can be added to the composition in an amount of 0,001 to 10
wt.% (referring to pure enzyme), preferably from 0,005 to 5 wt.%, more preferred from
0,01 to 2 wt.%, even more preferred from 0,1 to 1 wt.% of pure enzyme (meaning the
active enzyme).
[0112] The enzyme(s) can be added to the composition in form of granules, e.g. as granulates
comprising a binder and the enzyme or the enzyme and any further suitable detergent
ingredient. In such granules at least 2 wt.-% of a granule is represented by the enzyme(s).
In a preferred embodiment of the invention the enzyme(s) are provided in form of such
granules, wherein at least 5 wt.-% of a granule is represented by the enzyme(s), preferably
at least 10 wt.-%, more preferred at least 20 wt.-%, even more preferred at least
40 wt.-%. If no support is used in the inner core, the core of the granules may consist
of the enzyme(s) or up to 90 wt.-%, up to 80 wt.-% or up to 70 wt.-% are represented
by the enzyme(s).
Complexing Agent
[0113] A further preferred ingredient of cleaning compositions is at least one complexing
agent. The cleaning composition of the present invention may optionally comprise one
or more complexing agent(s) as at least one further ingredient.
[0114] Complexing agents are commonly used as co-builders to support the performance of
the builders.
[0115] A function of complexing agents is to capture trace metal ions like, Cu(II), Fe(II),
Fe(III), Mn(II), Cd(II), Co(II), Cr(III), Hg(II), Ni(II), Pb(II), Pd(II), Zn(II),
Ca(II), Mg(II) These ions can interfere with or disturb certain processes of the cleaning
in the washing machine, like e.g. the bleach performance.
[0116] The complexing agent(s) that are known to be used in cleaning compositions include,
but are not limited to S,S-ethylenediamine-N,N'-disuccinic acid (S,S-EDDS), ethylenediaminetetraacetic
acid (EDTA), diethylene triamine penta(methylene phosphonate) (DETPMP), nitrilotriacetic
acid (NTA), ethanol diglycine (EDG), imino disuccinic acid (IDS), methylglycine diacetic
acid (MGDA), diethylene triamine pentaacetic acid (DTPA), ethylene diamine dihydroxyphenyl
acetic acid (EDDHA), N-(hydroxyethyl) ethylenediamine triacetic acid (HEDTA), hydroxyethylidene-1,1-diphosphonic
acid (HEDP), phytic acid, diethylene triamine (DETA), triethylene tetramine (TETA),
tetraethylene pentamine (TEPA), aminoethyl ethanolamine (AEEA), glutamic acid N,N-diacetic
acid (GLDA), 1,3-propylenediamine tetraacetic acid (PDTA), glucoheptonic acid, dipicolinic
acid, ethylene diamine tetra (methylene phosphonic acid) (EDTMPA), 2-hydroxyethyliminodiacetic
acid (HEIDA) or water soluble salts thereof or mixtures thereof.
[0117] Further, phosphonates are preferred complexing agents. Useful phosphonates encompass,
besides 1-hydroxyethane-1,1-diphosphonic acid, a number of different compounds such
as, for example, diethylenetriaminepenta(methylenephosphonic acid) (DTPMP). Hydroxyalkane-or
aminoalkanephosphonates are preferred in this Application. Among the hydroxyalkanephosphonates,
1-hydroxyethane-1,1-diphosphonate (HEDP) is of particular importance as a co-builder.
It is used preferably as a sodium salt, the disodium salt reacting neutrally and the
tetrasodium salt in alkaline fashion (pH 9). Suitable aminoalkanephosphonates are,
e.g. ethylenediaminetetramethylenephosphonate (EDTMP), diethylenetriaminepentamethylenephosphonate
(DTPMP), as well as higher homologs thereof. They are used preferably in the form
of the neutrally reacting sodium salts, e.g. as a hexasodium salt of EDTMP resp. as
a hepta- and octasodium salt of DTPMP. Of the class of the phosphonates, HEDP is preferably
used as a builder. The aminoalkanephosphonates moreover possess a pronounced ability
to bind heavy metals. It may accordingly be preferred, in particular if the agents
also contain bleaches, to use aminoalkanephosphonates, in particular DTPMP, or mixtures
of the aforesaid phosphonates.
[0118] Particularly preferred are one or more phosphonate(s) from the group of
- a) aminotrimethylenephosphonic acid (ATMP) and/or salts thereof,
- b) ethylenediaminetetra(methylenephosphonic acid) (EDTMP) and/or salts thereof,
- c) diethylenetriaminepenta(methylenephosphonic acid) (DTPMP) and/or salts thereof,
- d) 1-hydroxyethane-1,1-diphosphonic acid (HEDP) and/or salts thereof,
- e) 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTC) and/or salts thereof,
- f) hexamethylenediaminetetra(methylenephosphonic acid) (HDTMP) and/or salts thereof,
- g) nitrilotri(methylenephosphonic acid) (NTMP) and/or salts thereof.
[0119] Washing- or cleaning compositions that contain 1-hydroxyethane-1,1-diphosphonic acid
(HEDP) or diethylenetriaminepenta(methylenephosphonic acid) (DTPMP) as phosphonates
are particularly preferred.
[0120] The cleaning compositions according to the present invention can of course contain
two or more different phosphonates.
[0121] Preferred cleaning compositions may contain at least one complexing agent from the
group above in terms of the total weight of the cleaning agent in a range from 0,01
to 8,0 wt.-%, preferably 0,02 to 5,0 wt.-%, and in particular 0,05 to 3,0 wt.-%.
[0122] Builders and co-builders can generally be added to the composition in acid form,
neutralized or in a partly neutralized form. When used in a partly or completely neutralized
form alkali metal salts are preferred, like sodium, potassium and lithium or ammonium
salts.
Bleaching
[0123] The composition of the present invention may comprise a bleaching system.
Bleaching agents can be used in a cleaning composition either alone or in combination
with a bleach activator and/or a bleach catalyst. The function of the bleaching agent
is the removal of bleachable stains and to achieve an antibacterial effect on the
load and inside of the laundry or the dish washing machine.
[0124] Bleaching agents that can be used in cleaning compositions include, but are not limited
to, active chlorine compounds, inorganic peroxygen compounds and organic peracids.
Examples are sodium percarbonate, sodium perborate monohydrate, sodium perborate tetrahydrate,
hydrogen peroxide, hydrogen peroxide-based compounds, persulfates, peroxymonosulphate,
peroxodisulphate, ε-phthalimido-perox-caproic acid, benzoyl peroxide, sodium hypochlorite,
sodium dichloroisocyanurate, etc. as well as mixtures thereof. Preferably at least
one bleaching agent is selected from inorganic bleaching agents, preferably from sodium
perborate or sodium percarbonate or a mixture thereof.
[0125] The weight proportion of the bleaching agent in terms of the total weight of the
cleaning composition is preferably from 1 to 40 wt.-%, more preferably from 2 to 30
wt.-%, and most preferred from 3 to 20 wt.-%.
[0126] The composition of the present invention may further comprise at least one bleach
catalyst, preferably a metal containing bleach catalyst that is selected from bleach-boosting
transition metal salts or transition metal complexes such as, for example, manganese-,
iron-, cobalt-, ruthenium- or molybdenum-salen or -carbonyl complexes. Manganese,
iron, cobalt, ruthenium, molybdenum, titanium, vanadium and copper complexes with
nitrogen-containing tripod ligands, as well as cobalt-, iron-, copper- and ruthenium-ammine
complexes may also be employed as the bleach catalysts. Such catalysts are broadly
described in the state of the art and well known by skilled artisans.
[0127] In
U.S. Pat. 4,430,243 one type of metal-containing bleach catalyst is disclosed which is a catalyst system
comprising a transition metal cation of defined bleach catalytic activity, such as
copper, iron, titanium, ruthenium tungsten, molybdenum, or manganese cations, an auxiliary
metal cation having little or no bleach catalytic activity, such as zinc or aluminum
cations, and a sequestrate having defined stability constants for the catalytic and
auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra
(methylenephosphonic acid) and water-soluble salts thereof.
[0128] Other types of bleach catalysts include the manganese-based complexes disclosed in
U.S. Pat. 5,246,621 and
U.S. Pat. 5,244,594. Preferred examples of theses catalysts include Mn
IV2(µ-O)
3(1,4,7-trimethyl-1,4,7-triazacyclononane)
2-(PF
6)
2 ("MnTACN"), Mn
III2(µO)
1(µ-OAc)
2(1,4,7-trimethyl-1,4,7-triazacyclononane)
2-(ClO
4)
2, Mn
IV4(µO)
6(1,4,7-triazacyclo
nonane)
4-(ClO
4)
2, Mn
IIIMn
IV4(µ-O)
1(µ-OAc)
2(1,4,7-trimethyl-1,4,7-triazacyclononane)
2-(ClO
4)
3, and mixtures thereof. See also European patent application
549,272. Other ligands suitable for use herein include 1,5,9-trimethyl-1,5,9-triazacyclododecane,
2-methyl-1,4,7-triazacyclononane, 2-methyl-1,4,7-triazacyclononane, and mixtures thereof
and mixtures of pentaamineacetate cobalt (III) nitrate and MnTACN.
[0129] Complexes of manganese in the valence state II, III, IV or V which preferably comprise
one or a plurality of macrocyclic ligands with the donor functions N, NR, PR, O and/or
S are particularly preferably employed. Ligands having nitrogen donor functions are
preferably employed. In this regard, it is particularly preferred to select the at
least one bleach catalyst from such having a group 1,4,7-trimethyl-1,4,7-triazacyclononane
(Me-TACN), 1,4,7-triazacyclononane (TACN), 1,5,9-trimethyl-1,5,9-triazacyclododecane
(Me-TACD), 2-methyl-1,4,7-trimethyl-1,4,7-triazacyclononane (Me/Me-TACN) 1,2,4,7,-tetramethyl-1,4,7-triazacyclo
nonane and/or 2-methyl-1,4,7-triazacyclononane (Me/TACN) as the macromolecular ligands.
Preferred manganese complexes are for example [Mn
III 2(µ-O)
1(µ-OAc)
2(TACN)
2](ClO
4)
2, [Mn
IIIMn
IV(µ-O)
2(µ-OAc)
1(TACN)
2](BPh
4)
2, [Mn
IV4(µ-O)
6(TACN)
4](ClO
4)
4, [Mn
III 2(µ-O)
1(µ-OAc)
2(Me-TACN)
2](ClO
4)
2, [Mn
IIIMn
IV(µ-O)
1(µ-OAc)
2(Me-TACN)
2](ClO
4)
3, [Mn
IV2(µ-O)
3(Me-TACN)
2](PF
6)
2(MnTACN), [Mn
IV2(µ-O)
3(Me/Me-TACN)
2](PF
6)
2 (OAc=OC(O)CH
3) and the complex of Mn
VI with1,2,4,7,-tetramethyl-1,4,7-triazacyclononane.
[0130] In a particularly preferred embodiment at least one metal containing bleach catalyst
is MnTACN.
[0131] The composition may comprise a bleach activator. With bleach activator any compound
is meant providing the possibility to use a comparatively low temperature to achieve
the desired bleaching performance when inorganic peroxygen based bleaching agents
are applied. Such a bleach activator reacts with the peroxygen to form an organic
peracid. Depending from the used bleach activator these peracids can have a hydrophobic
or a hydrophilic character.
[0132] Examples of bleach activators agents commonly used in cleaning compositions include,
but are not limited to, tetraacetylethylenediamine (TAED), sodium nonanoyloxybenzene
sulfonate (NOBS), acetyl caprolactone, N-methyl morpholinium acetonitrile and salts
thereof, sodium 4-(2-decanoyloxyethoxycarbonyloxy)benzenesulfonate (DECOBS) and salts
thereof, lauryloxybenzylsulfonate (LOBS), iso-lauryloxybenzylsulfonate (l-LOBS), N-methylmorpholinum-acetonitril
(MMA), Pentaacetylglucose, Nitrilquats, Benzoylcaprolactam (BzCL), 4-nitrobenzoylcaprolactam,
3-clorobenzoylcaprolactam, benzoyloxybenzylsulfonate (BOBS), phenylbenzoate (PhBz),
decanoyloxybenzylsulfonate (C10-OBS), benzoylvalerolactam (BZVL), octanoyloxybenzylsulfonate
(C8-OBS), 4-[N-(nonanoyl)aminohezanoyloxy]-benzylsulfonate-sodium salt (NACA-OBS),
10-undecenoyloxybenzylsulfonate (UDOBS), decanoyloxybenzoec acid (DOBA), perhydrolyzable
ester, perhydrolytic enzyme combined with an by this enzyme hydrolysable substrate,
acetyl caprolactone, Acetyl caprolactam (N-acetylhexanelactam) (e.g. Peractive LAC)
N-methyl morpholinium acetonitrile and salts thereof (such as Sokalan BMG from BASF).
TAED is preferred.
Dyes
[0133] The composition of the present invention may optionally comprise one or more dyes
as at least one further ingredient. The dye is used to colour the cleaning composition,
parts of the composition or speckles in the composition. This might render the product
more attractive to the consumer.
[0134] Dyes that can be used in cleaning compositions include, but are not limited to, Nylosan
yellow N-7GL, Sanolin brilliant flavine 8GZ, Sanolin yellow BG, Vitasyn quinoline
yellow 70, Vitasyn tartrazine X90, Puricolor yellow AYE23, Basacid yellow 232, Vibracolor
yellow AYE17, Simacid Eosine Y, Puricolor red ARE27, Puricolor red ARE14, Vibracolor
red ARE18, Vibracolor red ARE52, Vibracolor red SRE3, Basacid red 316, Ponceau SX,
Iragon blue DBL86, Sanolin blue EHRL, Sanolin turquoise blue FBL, Basacid blue 750,
Iragon blue ABL80, Vitasyn blue AE90, Basacid blue755, Vitasyn patentblue V 8501,
Vibracolor green AGR25. These dyes are available at the firms Clariant or BASF.
Perfumes
[0135] The composition of the present invention may optionally comprise one or more perfumes
as at least one further ingredient. The perfume is added to the cleaning composition
to improve the sensorial properties of the product or of the machine load after cleaning.
[0136] The perfume can be added to the cleaning composition as a liquid, paste or as a co-granulate
with a carrier material for the perfume. To improve the stability of the perfume it
can be used in an encapsulated form or as a complex like for example a perfume-cyclodextrine
complex.
[0137] Also perfumes that have a deodorizing effect can be applied. Such perfumes or raw
materials encapsulate malodours by binding to their sulphur groups.
[0138] In a preferred embodiment the detergent/cleaning composition comprises at least an
anionic and/or nonionic surfactant as defined above and an alkaline and/or acid compound,
preferably one or more of the builder compounds as cited above, more preferred sodium
carbonate and/or sodium bicarbonate as an alkalic compound and/or citric acid or citrate
as an acid compound.
WATER SOFTENER (b)
[0139] Typical water softener compositions comprise at least one of the compounds described
above as builders, co-builders or complexing agents.
[0140] In preferred embodiments the water softener comprisesin addition to optional adjuvants
and additives at least one of (a) one or more polycarboxylic acid homopolymer(s) or
salt(s) thereof in an amount of 1 to 90 wt.-%, (b) one or more low molecular polycarboxylic
acid(s) or salt(s) thereof in an amount of 1 to 90 wt.-%, and/or (c) one or more copolymer(s)
based on maleic acid or (meth)acrylic acid or salt(s) thereof in an amount of 0.1
to 25 wt.-%.
The one or more comonomer(s) may be selected from the group comprising
- i. hydrophobic monomers,
- ii. hydrophobic monomers with hydrophilic groups, and
- iii. hydrophilic monomers with hydrophilic groups,
or mixtures thereof.
a) "Polycarboxylic acid homopolymers" are defined as organic homopolymers of unsaturated
mono, di- or polycarboxylic acids. Examples of polycarboxylic acid homopolymers in
the sense of the present invention are polymers of acrylic acid, methacrylic acid,
hydroxyacrylic acid, maleic acid, itaconic acid, mesaconic acid, acotinic acid, methylene
malonic acid, citraconic acid. Also included by the term polycarboxylic acid homopolymers
are the derivatives and/or salts thereof. The term "poly(meth)acrylic acid" includes
polyacrylic acids, polymethacrylic acids as well as mixtures thereof. The molecular
weight of the polycarboxylic acid homopolymers in context with the present invention
is usually in the range of from above 1000 up to 250,000, preferably in the range
from above 1000 to 70,000. A particularly preferred polymer is polyacrylic acid with
a molecular weight in the range from above 1000 to 100,000, preferably in the range
from above 1000 to 70,000. The polycarboxylic acid homopolymers in context with the
present invention are provided either as solids or in solution, preferably in 20-90
wt.-% aqueous solution, more preferably in 30-70 wt.% aqueous solution.
b) "Low molecular polycarboxylic acids" are defined as organic carboxylic acids with
2 or more carboxylic groups and of low molecular weight. Examples of low molecular
polycarboxylic acids are citric acid, lactic acid, malic acid, maleic acid, tartaric
acid, agaric acid, trimellitic acid, succinic acid and the like. Also included by
the term low molecular polycarboxylic acids are the derivatives and/or salts thereof.
The molecular weight of the low molecular polycarboxylic acids in context with the
present invention is usually up to 1000. Particular preferred acids are citric acid
and/or trisodium citrate.
c) "Maleic acid or (meth)acrylic acid based copolymers" are copolymers, including
also e.g. terpolymers, of (i) one or more hydrophobic monomers or (ii) one or more
hydrophobic monomers with one or more hydrophilic group(s) or (iii) one or more hydrophilic
monomers with hydrophilic groups or mixtures thereof with maleic acid, acrylic acid
and/or methacrylic acid. The term "(meth)acrylic acid" includes acrylic acid, methacrylic
acid as well as mixtures thereof. The molecular weight of the maleic acid or (meth)acrylic
acid based copolymers in context with the present invention is usually in the range
of from above 1000 up to 100,000, preferably in the range from above 1000 to 60,000.
Also included by the term maleic acid or (meth)acrylic acid based copolymers are the
derivatives and/or salts thereof. The maleic acid or (meth)acrylic acid based copolymers
in context with the present invention are provided either as solids or in solution,
preferably in 20-90 wt.-% aqueous solution, more preferably in 30-70 wt.-% aqueous
solution.
ci) The "hydrophobic monomer(s)" of the maleic acid or (meth)acrylic acid based copolymers
are monomers which have a hydrophobic character either in their monomeric form or
even after their polymerisation in the polymer chain. Types of hydrophobic monomers
are olefines or alpha-olefines with carbon chain lengths from 3 to 16 carbon atoms,
unsaturated cyclic hydrocarbons, aryl compounds. Preferred types of hydrophobic monomers
are olefins or alpha-olefins with carbon chain lengths from 3 to 16 carbon atoms and
aryl compounds.
Examples of hydrophobic monomers are styrene, methyl styrene, 2-ethylhexyl acrylate,
octylacrylate, lauryl acrylate, stearyl acrylate, behenyl acrylate, 2-ethylhexyl methacrylate,
octylmethacrylate, lauryl methacrylate, stearyl methacrylate, behenyl methacrylate,
2-ethylhexyl acrylamide, octylacrylamide, lauryl acrylamide, stearyl acrylamide, behenyl
acrylamide, propyl acrylate, butyl acrylate, pentyl acrylate, hexyl acrylate, 1-vinyl
naphthalene, 2-vinyl naphthalene, 3-methyl styrene, 4-propyl styrene, t-butyl styrene,
4-cyclohexyl styrene, 4-dodecyl styrene, 2-ethyl-4-benzyl styrene, 4-(phenylbutyl)
styrene, 1-propene, 2-propene, 1-butene, 2-butene, 1-pentene, 2-pentene, 1-hexene,
2-hexene, 3-hexene, 1-heptene, 2-heptene, 3-heptene, 1-octene, 2-octene, 3-octene,
4-octene. Preferred are styrene, methyl styrene and mentioned olefins.
cii and ciii) The "hydrophilic group(s)" of the monomer(s) of the maleic acid or (meth)acrylic
acid based copolymers give the monomer where it is attached to an increased hydrophilic
character. The hydrophilic group(s) is/are typically one or more selected from the
group comprising hydroxyl, carboxamide, amine, carboxylate, carboxyl, phosphate, phosphono,
phosphino, phosphonate, sulfonyl or sulfo group and the like.
[0141] Examples of hydrophilic monomers with hydrophilic groups are (meth)allyl sulphonic
acid, vinyl sulphonic acid, vinyl phosphonic acid, dimethylacrylamide, dimethylaminopropylmethacrylate,
diethylaminopropylmethacrylate, vinyl formamide, vinyl acetamide, vinyl pyrrolidone,
vinyl imidazole, phenyl (meth)allyl ether sulfonic acid, 2-acrylamido-2-methyl propane
sulfonic acid (AMPS), sulphonated styrene, allyloxybenzene sulfonic acid, allyloxy-2-hydroxy
propyl sulfonic acid, 2-acryloxypropionic acid or (meth)allyl phosphonic acid, and
the like or salts thereof.