FIELD OF THE INVENTION
[0001] The present invention relates to an array of packages. The array comprises three
or more different packages each comprising a different water-soluble automatic dishwashing
detergent multi-compartment pouch.
BACKGROUND OF THE INVENTION
[0002] Unit dose detergent articles are particularly popular with consumers. The ease of
use and consistent performance are two characteristics that consumers find desirable.
For automatic dishwashing applications, unit dose detergent articles in water-soluble
pouch form are very popular with consumers.
[0003] Water-soluble automatic dishwashing detergent pouches comprise an automatic dishwashing
detergent composition that is enclosed by a water-soluble film. During the washing
cycle, the detergent chemistry is released into the washing zone of the automatic
dishwashing appliance and helps treat the dishware to be cleaned.
[0004] Consumers have many different needs when cleaning dishware in their automatic dishwashing
machines. Different consumers require different performance profiles at different
times when washing different loads of dishware. In addition, consumers may also require
different price points at different times when washing different loads of dishware.
At times, a consumer may require a greater care profile from their automatic dishwashing
pouch, at other times the consumer may require a greater cleaning performance from
their automatic dishwashing pouch.
[0005] Water-soluble automatic dishwashing detergent multi-compartment pouches that comprise
both a liquid component and a solid component are desirable as they indicate to the
consumer that the pouch has a good cleaning profile as well as a good care profile.
A good care profile can include good shine performance as well as a good metal care
performance.
[0006] The liquid component of the composition can be enclosed by several compartments within
the pouch. The more compartments that enclose the liquid component, as well as the
higher portion, by weight, of the automatic dishwashing detergent composition that
is a liquid component, indicates to the consumer that the pouch has a superior care
profile. Consumers that require improved care performance desire pouches having a
high number of liquid-containing compartments as well as pouches that comprise a detergent
composition having a high portion of liquid component compared to solid component.
High portion being in relative terms because typically the composition will usually
comprise more solid component that liquid component.
[0007] The fewer number of compartments that enclose the liquid component, as well as the
lower portion, by weight, of the automatic dishwashing detergent composition that
is a liquid component, indicates to the consumer that the pouch has a superior cleaning
profile. Consumers that require improved cleaning performance desire pouches having
a low number of liquid-containing compartments as well as pouches that comprise a
detergent composition having a small portion of liquid component compared to solid
component.
[0008] Furthermore, consumers often equate more liquid-containing compartments and a higher
(relative) portion of liquid component to solid component as being an expensive water-soluble
automatic dishwashing detergent multi-compartment pouch.
[0009] However, consumers may not always require a pouch that communicates good care profile,
or a consumer may not always require a pouch that communicates good cleaning performance.
In addition, a consumer may not always wish to use a pouch that equates to an expensive
option, and instead may wish to use a pouch that equates to a lower cost option.
[0010] The present invention seeks to address this need by providing an array of packages
comprising three or more different packages each comprising a different water-soluble
automatic dishwashing detergent multi-compartment pouch. The array provides the consumer
with at least three options that the consumer will equate to having different price
points, different cleaning performance, and different care profile.
SUMMARY OF THE INVENTION
[0011] The present invention provides an array of packages comprising three or more different
packages each comprising a different water-soluble automatic dishwashing detergent
multi-compartment pouch, the array comprising:
- (a) a first package comprising a first water-soluble automatic dishwashing detergent
multi-compartment pouch, wherein the first pouch comprises a first automatic dishwashing
detergent composition that is enclosed by a water-soluble film within two or more
compartments, wherein the first automatic dishwashing detergent composition has a
solid component and a liquid component, wherein the solid component is enclosed within
one or more separate components, and wherein the liquid component is enclosed within
one or two separate components;
- (b) a second package comprising a second water-soluble automatic dishwashing detergent
multi-compartment pouch, wherein the second pouch comprises a second automatic dishwashing
detergent composition that is enclosed by a water-soluble film within four or more
compartments, wherein the second automatic dishwashing detergent composition has a
solid component and a liquid component, wherein the solid component is enclosed within
one or more separate components, and wherein the liquid component is enclosed within
three or four separate components; and
- (c) a third package comprising a third water-soluble automatic dishwashing detergent
multi-compartment pouch, wherein the third pouch comprises a third automatic dishwashing
detergent composition that is enclosed by a water-soluble film within six or more
compartments, wherein the third automatic dishwashing detergent composition has a
solid component and a liquid component, wherein the solid component is enclosed within
one or more separate components, and wherein the liquid component is enclosed within
five or more separate components,
wherein the weight ratio of the liquid component to solid component of the third automatic
dishwashing detergent composition is greater than the weight ratio of the liquid component
to solid component of the second automatic dishwashing detergent composition, and
wherein the weight ratio of the liquid component to solid component of the second
automatic dishwashing detergent composition is greater than the weight ratio of the
liquid component to solid component of the first automatic dishwashing detergent composition.
DETAILED DESCRIPTION OF THE INVENTION
Array of packages
[0012] The array of packages comprises three or more different packages each comprising
a different water-soluble automatic dishwashing detergent multi-compartment pouch.
The array comprises:
- (a) a first package comprising a first water-soluble automatic dishwashing detergent
multi-compartment pouch, wherein the first pouch comprises a first automatic dishwashing
detergent composition that is enclosed by a water-soluble film within two or more
compartments, wherein the first automatic dishwashing detergent composition has a
solid component and a liquid component, wherein the solid component is enclosed within
one or more separate components, and wherein the liquid component is enclosed within
one or two separate components;
- (b) a second package comprising a second water-soluble automatic dishwashing detergent
multi-compartment pouch, wherein the second pouch comprises a second automatic dishwashing
detergent composition that is enclosed by a water-soluble film within four or more
compartments, wherein the second automatic dishwashing detergent composition has a
solid component and a liquid component, wherein the solid component is enclosed within
one or more separate components, and wherein the liquid component is enclosed within
three or four separate components; and
- (c) a third package comprising a third water-soluble automatic dishwashing detergent
multi-compartment pouch, wherein the third pouch comprises a third automatic dishwashing
detergent composition that is enclosed by a water-soluble film within six or more
compartments, wherein the third automatic dishwashing detergent composition has a
solid component and a liquid component, wherein the solid component is enclosed within
one or more separate components, and wherein the liquid component is enclosed within
five or more separate components.
[0013] The weight ratio of the liquid component to solid component of the third automatic
dishwashing detergent composition is greater than the weight ratio of the liquid component
to solid component of the second automatic dishwashing detergent composition.
[0014] The weight ratio of the liquid component to solid component of the second automatic
dishwashing detergent composition is greater than the weight ratio of the liquid component
to solid component of the first automatic dishwashing detergent composition.
[0015] Preferably, the ratio of:
- (i) the weight ratio of the liquid component to solid component of the third automatic
dishwashing detergent composition, to
- (ii) the weight ratio of the liquid component to solid component of the second automatic
dishwashing detergent composition,
is in the range of from greater than 1.0:1 to less than 3.33:1, more preferably in
the range of from greater than 1.2: 1 to 1.8:1.
[0016] Preferably, the ratio of:
- (i) the weight ratio of the liquid component to solid component of the second automatic
dishwashing detergent composition, to
- (ii) the weight ratio of the liquid component to solid component of the first automatic
dishwashing detergent composition,
is in the range of from greater than 1.0: 1 to 5.5:1, more preferably in the range
of from greater than 1.8: 1 to 2.8:1.
[0017] Preferably, the ratio of:
- (i) the weight ratio of the liquid component to solid component of the third automatic
dishwashing detergent composition, to
- (ii) the weight ratio of the liquid component to solid component of the first automatic
dishwashing detergent composition,
is in the range of from greater than 1.8:1 to 10:1, more preferably in the range of
from greater than 2.0:1 to 4.0:1.
[0018] Preferably, the weight ratio of the liquid component to solid component of the first
automatic dishwashing detergent composition is in the range of from 0.04: 1 to 0.12:
1, more preferably in the range of from 0.06: 1 to 0.10: 1.
[0019] Preferably, the weight ratio of the liquid component to solid component of the second
automatic dishwashing detergent composition is in the range of from above 0.12:1 to
0.22:1, more preferably in the range of from 0.15:1 to 0.20:1.
[0020] Preferably, the weight ratio of the liquid component to solid component of the third
automatic dishwashing detergent composition is in the range of from above 0.22:1 to
0.40:1, more preferably in the range of from 0.23:1 to 0.30:1.
[0021] Preferably, at least one of the pouches is superposed, more preferably all of the
pouches are superposed.
[0022] At least one of the packages can be a cardboard carton.
[0023] At least one of the packages can be a paper bag.
[0024] At least one of the packages can be a plastic bag.
Water-soluble automatic dishwashing detergent pouch.
[0025] The water-soluble automatic dishwashing detergent pouches are described in more detail
below.
[0026] The pouch comprises an automatic dishwashing detergent composition that is enclosed
by a water-soluble film.
[0027] The pouch can be a single compartment pouch comprising only one compartment. Typically
for this embodiment, the automatic dishwashing detergent composition is contained
within this single compartment.
[0028] The pouch may also be a multi-compartment pouch, comprising more than one compartment.
Typically, these separate compartments are separated by water-soluble film.
[0029] The multi-compartment pouch may have a side-by-side configuration. In this manner,
the separate compartments are typically sealed together so that at least one compartment
is side by side to another compartment. The side-by-side configuration may be foldable
between adjacent compartments to facilitate placement of the multi-compartment pouch
into a dishwashing detergent receptacle.
[0030] The multi-compartment pouch may have a superposed configuration. In this manner,
the separate compartments are typically sealed together so that at least one compartment
is superposed on top of another compartment.
[0031] Multi-compartment pouches can be preferred when the automatic dishwashing detergent
composition comprises both a solid component and a liquid component. The multi-compartment
pouch can comprise the liquid component in one or more separate compartments to the
solid component. However, multi-compartment pouches can also be suitable when the
automatic dishwashing detergent composition comprises only a solid component or only
a liquid component.
[0032] Single compartment pouches can be preferred when the automatic dishwashing detergent
composition comprises only a solid component or only a liquid component. However,
single compartment pouches can also be suitable when the automatic dishwashing detergent
composition comprises both a solid component and a liquid component, for example,
the solid component may be a discontinuous phase that is dispersed within the liquid
component that is a continuous phase, or the liquid component is in the form of a
gel and is in direct contact with, such as layered onto, the powder component.
[0033] The multi-compartment pouch may comprise two or more compartments, or three or more
compartments, or four or more compartments, or five or more compartments, or even
six or more compartments, and preferably from 2 to 10 compartments, or from 3 to 9
compartments, or from 4 to 8 compartments, or even from 5 to 7 compartments.
[0034] It may be preferred for the compartments comprising the liquid component to be in
a side-by-side configuration.
[0035] It may be preferred for the compartment(s) comprising the liquid component to be
superposed on top of the compartment(s) comprising the solid component.
[0036] It may be preferred for the compartment(s) comprising the liquid component to be
positioned in a side-by-side configuration with the compartment(s) comprising the
solid component.
[0037] It may be preferred for the solid component to be contained within only one single
compartment within the pouch.
[0038] It may be preferred for the liquid component to be contained within two or more compartments
within the pouch, or even three or more compartments, or four or more compartments,
or five or more compartments, or even six or more compartments, and preferably from
2 to 10 compartments, or from 3 to 9 compartments, or from 4 to 8 compartments, or
even from 5 to 7 compartments.
[0039] It may be preferred for the solid component to be contained within only one single
compartment within the pouch, and it may be preferred for the liquid component to
be contained within two or more compartments within the pouch, or even three or more
compartments, or four or more compartments, or five or more compartments, or even
six or more compartments, and preferably from 2 to 10 compartments, or from 3 to 9
compartments, or from 4 to 8 compartments, or even from 5 to 7 compartments.
[0040] It may be preferred for the compartment(s) that contain the liquid component to be
superposed on top of the compartment(s) that contain the solid component. If the liquid
component is contained within more than one compartment, it may be preferred for these
compartments to be in a side-by-side configuration. If the solid component is contained
within more than one compartment, it may be preferred for these compartments to be
in a side-by-side configuration.
[0041] Typically, the pouch has the following dimensions:
- (i) a maximum length of from 30mm to 90mm;
- (ii) a maximum width of from 30mm to 54mm;
- (iii) a maximum height of from 8mm to 41mm; and
- (iv) a total internal compartment volume of from 10ml to 199ml.
[0042] Typically, the weight of the pouch is in the range of from 10g to 30g, preferably
from 11g to 26g, or from 12g to 24g, or even from 13g to 20g.
[0043] Typically, the pouch comprises from 9.0g to 29.7g, or from 10.0g to 25.7g, or from
11.0g to 23.7g, or from 12.0g to 19.7g of the automatic dishwashing detergent composition.
[0044] The automatic detergent dishwashing detergent composition can be made up of from
0.5g to 10g, or from 0.6g to 9.0g, or from 0.7g to 8 0g, or from 0.8g to 7.0g, or
from 0.9g to 6.0g, or from 0.9g to 5.0g, or from 1.0g to 4.0g liquid component.
[0045] The automatic detergent dishwashing detergent composition can be made up of from
4.0g to 28g, or from 5.0g to 26g, or from 6.0g to 24g, or from 7.0g to 22g, or from
8.0g to 20g, or from 10g to 18g, or from 13g to 16g solid component.
[0046] Typically, the pouch comprises from 0.3g to 1.0g, or from 0.35g to 0.9g, or from
0.4g to 0.8g, or from 0.5g to 0.7g water-soluble film.
Automatic dishwashing detergent composition.
[0047] Typically, the composition is in solid form and/or liquid form. Preferably, the composition
comprises a solid component and a liquid component. The solid component and/or liquid
component are typically contained within separate compartments within the pouch. Typically,
these separate compartments are separated by water-soluble film. These separate compartments
can be in a side-by-side configuration, or (and preferably) in a superposed configuration.
Typically, the compartment(s) containing the liquid component is/are superposed on
top of the compartment(s) comprising the solid component. The solid component is typically
contained within one compartment within the pouch. The liquid component is typically
contained within more than one compartment within the pouch, such as two or more compartments,
or three or more compartments, or four or more compartments, or five or more compartments,
or even six or more compartments, and preferably from 2 to 10 compartments, or from
3 to 9 compartments, or from 4 to 8 compartments, or even from 5 to 7 compartments.
[0048] The liquid component, or part thereof, may be contained within a compartment that
also contains the solid component, or part thereof. It may be preferred that the liquid
component, or part thereof, forms a continuous phase within the compartment, and the
solid component, or part thereof, forms a discontinuous phase.
[0049] The solid component, or part thereof, may be in the form of a free-flowing powder,
or a tablet, preferably a free-flowing powder. The free-flowing powder may be compressed
when contained in a compartment of the pouch.
[0050] The solid component, especially when in free-flowing powder form, can have a bulk
density in the range of from 400g/l to 1200g/l, or from 600g/l to 1000g/l.
[0051] The liquid component, or part thereof, may be a free-flowing liquid, or may be a
viscous liquid. The liquid component, or part thereof, may be a gel.
[0052] The liquid component, or part thereof, can have a viscosity in the range of from
50cP to 750cP, or from 100cP to 500cP.
[0053] Viscosity is typically measured using a rheometer. The viscosity is typically measured
at a function of shear rate of from 1.0s
-1 to 1500s
-1, and at a temperature of from 10°C to 30°C.
[0054] The composition typically comprises one or more of an alkalinity system, a bleach
system, a builder system, a chelant system, an enzyme system, a polymer system, and
a surfactant system. The composition can also include other detergent ingredients.
[0055] Solid detergent ingredients are typically comprised by the solid component. Liquid
detergent ingredients are typically comprised by the liquid component. However, a
liquid detergent ingredient can be formulated into a solid particle: e.g., by loading
onto a solid carrier material, or a liquid ingredient can be sprayed-on or agglomerated
into the solid component. In this manner, a liquid detergent ingredient can be comprised
by the solid component.
[0056] The alkalinity system, or part thereof, can be comprised by the liquid component
and/or the solid component. Typically, the alkalinity system, or part thereof, is
comprised by the solid component.
[0057] The bleach system, or part thereof, can be comprised by the liquid component and/or
the solid component. Typically, the bleach system, or part thereof, is comprised by
the solid component.
[0058] The builder system, or part thereof, can be comprised by the liquid component and/or
the solid component. Typically, the builder system, or part thereof, is comprised
by the solid component.
[0059] The chelant system, or part thereof, can be comprised by the liquid component and/or
the solid component. Typically, the chelant system, or part thereof, is comprised
by the solid component.
[0060] The enzyme system, or part thereof, can be comprised by the liquid component and/or
the solid component. The enzyme system, or part thereof, may be comprised by the liquid
component. The enzyme system, or part thereof, may be comprised by the solid component.
Part of the enzyme system may be comprised by the liquid component and part of the
enzyme system may be comprised by the solid component.
[0061] The polymer system, or part thereof, can be comprised by the liquid component and/or
the solid component. The polymer system, or part thereof, may be comprised by the
solid component. Part of the polymer system may be comprised by the liquid component
and part of the polymer system may be comprised by the solid component.
[0062] The surfactant system, or part thereof, can be comprised by the liquid component
and/or the solid component. The surfactant system, or part thereof, may be comprised
by the liquid component. The surfactant system, or part thereof, may be comprised
by the solid component. Part of the surfactant system may be comprised by the liquid
component and part of the surfactant system may be comprised by the solid component.
[0063] The composition, upon dissolution in deionized water at 20°C to a concentration of
1.0g/l, may have an equilibrium pH in the range of from 3.0 to 12.0, or from 5.0 to
12.0, or from 6.0 to 12.0, or from 7.0 to 12.0, or from above 7.0 to 12.0, or from
8.0 to 12.0, or from 9.0 to 12.0, or from 10.0 to 12.0,or from 10.0 to 11.5, or from
10.0 to 11.0.
[0064] In use, the composition, upon contact with water, may form a wash liquor having a
pH profile in the range of from 3.0 to 12.0, or from 5.0 to 12.0, or from 6.0 to 12.0,
or from 7.0 to 12.0, or from above 7.0 to 12.0, or from 8.0 to 12.0, or from 9.0 to
12.0, or from 10.0 to 12.0, or from 10.0 to 11.5, or from 10.0 to 11.0.
Water-soluble film.
[0065] The water-soluble film preferably has a thickness of from 20 to 150 microns, preferably
from 35 to 125 microns, or even more preferably from 50 to 110 microns, most preferably
about 76 microns.
[0066] The water-soluble film is typically soluble or dispersible in water. Preferably,
the film has a water-solubility of at least 50%, preferably at least 75% or even at
least 95%, as measured by the method set out here after using a glass-filter with
a maximum pore size of 20 microns: 5 grams ± 0.1 gram of film material is added in
a pre-weighed 3L beaker and 2L ± 5ml of distilled water is added. This is stirred
vigorously on a magnetic stirrer, Labline model No. 1250 or equivalent and 5 cm magnetic
stirrer, set at 600 rpm, for 30 minutes at 30°C. Then, the mixture is filtered through
a folded qualitative sintered-glass filter with a pore size as defined above (max.
20 micron). The water is dried off from the collected filtrate by any conventional
method, and the weight of the remaining material is determined (which is the dissolved
or dispersed fraction). Then, the percentage solubility (or dispersibility) can be
calculated.
[0067] The water-soluble film material may be obtained by casting, blow-moulding, extrusion
or blown extrusion of the polymeric material, as known in the art.
[0068] The water-soluble film preferably comprises polyvinylalcohol (PVA). The polyvinylalcohol
may be present between 50% and 95%, preferably between 55% and 90%, more preferably
between 60% and 80% by weight of the water-soluble film. The polyvinylalcohol preferably
comprises polyvinyl alcohol homopolymer, polyvinylalcohol copolymer, or a mixture
thereof. Preferably, the water-soluble film comprises a blend of polyvinylalcohol
homopolymers and/or anionic polyvinylalcohol copolymers, preferably wherein the polyvinylalcohol
copolymers are selected from sulphonated and carboxylated anionic polyvinylalcohol
copolymers especially carboxylated anionic polyvinylalcohol copolymers, most preferably
the water-soluble film comprises a blend of a polyvinylalcohol homopolymer and a carboxylated
anionic polyvinylalcohol copolymer, or a blend of polyvinylalcohol homopolymers. Alternatively,
the polyvinylalcohol comprises an anionic polyvinyl alcohol copolymer, most preferably
a carboxylated anionic polyvinylalcohol copolymer. When the polyvinylalcohol in the
water-soluble film is a blend of a polyvinylalcohol homopolymer and a carboxylated
anionic polyvinylalcohol copolymer, the homopolymer and the anionic copolymer are
present in a relative weight ratio of 90/10 to 10/90, preferably 80/20 to 20/80, more
preferably 70/30 to 50/50. Without wishing to be bound by theory, the term "homopolymer"
generally includes polymers having a single type of monomeric repeating unit (e.g.,
a polymeric chain comprising or consisting of a single monomeric repeating unit).
For the case of polyvinylalcohol, the term "homopolymer" typically further includes
copolymers having a distribution of vinyl alcohol monomer units and optionally vinyl
acetate monomer units, depending on the degree of hydrolysis (e.g., a polymeric chain
comprising or consisting of vinyl alcohol and vinyl acetate monomer units). In the
case of 100% hydrolysis, a polyvinylalcohol homopolymer can include only vinyl alcohol
units. Without wishing to be bound by theory, the term "copolymer" generally includes
polymers having two or more types of monomeric repeating units (e.g., a polymeric
chain comprising or consisting of two or more different monomeric repeating units,
whether as random copolymers, block copolymers, etc.). For the particular case of
polyvinylalcohol, the term "copolymer" (or "polyvinylalcohol copolymer") typically
further includes copolymers having a distribution of vinyl alcohol monomer units and
vinyl acetate monomer units, depending on the degree of hydrolysis, as well as at
least one other type of monomeric repeating unit (e.g., a ter- (or higher) polymeric
chain comprising or consisting of vinyl alcohol monomer units, vinyl acetate monomer
units, and one or more other monomer units, for example anionic monomer units). In
the case of 100% hydrolysis, a polyvinylalcohol copolymer can include a copolymer
having vinyl alcohol units and one or more other monomer units, but no vinyl acetate
units. Without wishing to be bound by theory, the term "anionic copolymer" includes
copolymers having an anionic monomer unit comprising an anionic moiety. General classes
of anionic monomer units which can be used for the anionic polyvinyl alcohol co-polymer
include the vinyl polymerization units corresponding to monocarboxylic acid vinyl
monomers, their esters and anhydrides, dicarboxylic monomers having a polymerizable
double bond, their esters and anhydrides, vinyl sulfonic acid monomers, and alkali
metal salts of any of the foregoing. Examples of suitable anionic monomer units include
the vinyl polymerization units corresponding to vinyl anionic monomers including vinyl
acetic acid, maleic acid, monoalkyl maleate, dialkyl maleate, monomethyl maleate,
dimethyl maleate, maleic anyhydride, fumaric acid, monoalkyl fumarate, dialkyl fumarate,
monomethyl fumarate, dimethyl fumarate, fumaric anyhydride, itaconic acid, monomethyl
itaconate, dimethyl itaconate, itaconic anhydride, vinyl sulfonic acid, allyl sulfonic
acid, ethylene sulfonic acid, 2-acrylamido-1-methylpropanesulfonic acid, 2-acrylamido-2-methylpropanesulfonic
acid, 2-methylacrylamido-2-methylpropanesulfonic acid, 2-sufoethyl acrylate, alkali
metal salts of the foregoing (e.g., sodium, potassium, or other alkali metal salts),
esters of the foregoing (e.g., methyl, ethyl, or other C1-C4 or C6 alkyl esters),
and combinations thereof (e.g., multiple types of anionic monomers or equivalent forms
of the same anionic monomer). The anionic monomer may be one or more acrylamido methylpropanesulfonic
acids (e.g., 2-acrylamido-1-methylpropanesulfonic acid, 2-acrylamido-2-methylpropanesulfonic
acid, 2-methylacrylamido-2-methylpropanesulfonic acid), alkali metal salts thereof
(e.g., sodium salts), and combinations thereof. Preferably, the anionic moiety of
the first anionic monomer unit is selected from a sulphonate, a carboxylate, or a
mixture thereof, more preferably a carboxylate, most preferably an acrylate, a methacrylate,
a maleate, or a mixture thereof. Preferably, the anionic monomer unit is present in
the anionic polyvinyl alcohol copolymer in an average amount in a range of between
1 mol.% and 10 mol.%, preferably between 2 mol.% and 5 mol.%.
[0069] Preferably, the polyvinyl alcohol, and/or in case of polyvinylalcohol blends the
individual polyvinylalcohol polymers, have an average viscosity (µ1) in a range of
between 4 mPa.s and 30 mPa.s, preferably between 10mPa.s and 25 mPa.s, measured as
a 4% polyvinyl alcohol polymer solution in demineralized water at 20°C.
[0070] The viscosity of a polyvinyl alcohol polymer is typically determined by measuring
a freshly made solution using a Brookfield LV type viscometer with UL adapter as described
in British Standard EN ISO 15023-2:2006 Annex E Brookfield Test method. It is international
practice to state the viscosity of 4% aqueous polyvinyl alcohol solutions at 20°C.
It is well known in the art that the viscosity of an aqueous water-soluble polymer
solution (polyvinylalcohol or otherwise) is correlated with the weight-average molecular
weight of the same polymer, and often the viscosity is used as a proxy for weight-average
molecular weight. Thus, the weight-average molecular weight of the polyvinylalcohol
can be in a range of 30,000 to 175,000, or 30,000 to 100,000, or 55,000 to 80,000.
[0071] Preferably, the polyvinyl alcohol, and/or in case of polyvinylalcohol blends the
individual polyvinylalcohol polymers, have an average degree of hydrolysis in a range
of between 75% and 99%, preferably between 80% and 95%, most preferably between 85%
and 95%.
[0072] A suitable test method to measure the degree of hydrolysis is as according to standard
method JIS K6726.
[0073] Preferably, the water-soluble film comprises a non-aqueous plasticizer. Preferably,
the non-aqueous plasticizer is selected from polyols, sugar alcohols, and mixtures
thereof. Suitable polyols include polyols selected from the group consisting of glycerol,
diglycerin, ethylene glycol, diethylene glycol, triethyleneglycol, tetraethylene glycol,
polyethylene glycols up to 400 molecular weight, neopentyl glycol, 1,2-propylene glycol,
1,3-propanediol, dipropylene glycol, polypropylene glycol, 2-methyl-1,3-propanediol,
trimethylolpropane and polyether polyols, or a mixture thereof. Suitable sugar alcohols
include sugar alcohols selected from the group consisting of isomalt, maltitol, sorbitol,
xylitol, erythritol, adonitol, dulcitol, pentaerythritol and mannitol, or a mixture
thereof. More preferably the non-aqueous plasticizer is selected from glycerol, 1,2-propanediol,
dipropylene glycol, 2-methyl-1,3-propanediol, trimethylolpropane, triethyleneglycol,
polyethyleneglycol, sorbitol, or a mixture thereof, most preferably selected from
glycerol, sorbitol, trimethylolpropane, dipropylene glycol, and mixtures thereof.
One particularly suitable plasticizer system includes a blend of glycerol, sorbitol
and trimethylol propane. Another particularly suitable plasticizer system includes
a blend of glycerin, dipropylene glycol, and sorbitol. Preferably, the film comprises
between 5% and 50%, preferably between 10% and 40%, more preferably between 20% and
30% by weight of the film of the non-aqueous plasticizer.
[0074] Preferably, the water-soluble film comprises a surfactant. Preferably, the water-soluble
film comprises a surfactant in an amount between 0.1% and 2.5%, preferably between
1% and 2% by weight of the water-soluble film. Suitable surfactants can include the
nonionic, cationic, anionic and zwitterionic classes. Suitable surfactants include,
but are not limited to, polyoxyethylenated polyoxypropylene glycols, alcohol ethoxylates,
alkylphenol ethoxylates, tertiary acetylenic glycols and alkanolamides (nonionics),
polyoxyethylenated amines, quaternary ammonium salts and quaternized polyoxyethylenated
amines (cationics), and amine oxides, N-alkylbetaines and sulfobetaines (zwitterionics).
Other suitable surfactants include dioctyl sodium sulfosuccinate, lactylated fatty
acid esters of glycerol and propylene glycol, lactylic esters of fatty acids, sodium
alkyl sulfates, polysorbate 20, polysorbate 60, polysorbate 65, polysorbate 80, lecithin,
acetylated fatty acid esters of glycerol and propylene glycol, and acetylated esters
of fatty acids, and combinations thereof.
[0075] Preferably, the water-soluble film comprises lubricants / release agents. Suitable
lubricants/release agents include fatty acids and their salts, fatty alcohols, fatty
esters, fatty amines, fatty amine acetates and fatty amides. Preferred lubricants/release
agents are fatty acids, fatty acid salts, and fatty amine acetates. The amount of
lubricant/release agent in the water-soluble film is typically in a range of from
0.02% to 1.5%, preferably from 0.1% to 1% by weight of the water-soluble film.
[0076] Preferably, the water-soluble film comprises fillers, extenders, antiblocking agents,
detackifying agents or a mixture thereof. Suitable fillers, extenders, antiblocking
agents, detackifying agents or a mixture thereof include starches, modified starches,
crosslinked polyvinylpyrrolidone, crosslinked cellulose, microcrystalline cellulose,
silica, metallic oxides, calcium carbonate, talc and mica. Preferred materials are
starches, modified starches and silica.
[0077] Preferably, the amount of filler, extender, antiblocking agent, detackifying agent
or mixture thereof in the water-soluble film is in a range of from 0.1% to 25%, preferably
from 1% to 10%, more preferably from 2% to 8%, most preferably from 3% to 5% by weight
of the water-soluble film. In the absence of starch, one preferred range for a suitable
filler, extender, antiblocking agent, detackifying agent or mixture thereof is from
0.1% to 1%, preferably 4%, more preferably 6%, even more preferably from 1% to 4%,
most preferably from 1% to 2.5%, by weight of the water-soluble film.
[0078] Preferably the water-soluble film has a residual moisture content of at least 4%,
more preferably in a range of from 4% to 15%, even more preferably of from 5% to 10%
by weight of the water-soluble film, typically as measured by Karl Fischer titration.
[0079] Preferred water-soluble films exhibit good dissolution in cold water, meaning unheated
distilled water. Preferably, such water-soluble films exhibit good dissolution at
temperatures of 24°C, even more preferably at 10°C. By good dissolution it is typically
meant that the water-soluble film exhibits a water-solubility of at least 50%, preferably
at least 75% or even at least 95%, as measured by the method set out here after using
a glass-filter with a maximum pore size of 20 microns, described above.
[0080] Preferred films include those supplied by Monosol under the trade references M8630,
M8900, M8779, M8310.
[0081] The film may be opaque, transparent, or translucent.
[0082] The film may comprise a printed area. The area of print may be achieved using standard
techniques, such as flexographic printing or inkjet printing. Preferably, the ink
used in the printed area comprises between Oppm and 20ppm, preferably between Oppm
and 15ppm, more preferably between Oppm and 10ppm, even more preferably between Oppm
and 5ppm, even more preferably between Oppm and 1ppm, even more preferably between
Oppb and 100ppb, most preferably Oppb dioxane. Those skilled in the art will be aware
of known methods and techniques to determine the dioxane level within the ink formulations.
[0083] The film may comprise an aversive agent, for example a bittering agent. Suitable
bittering agents include, but are not limited to, naringin, sucrose octaacetate, quinine
hydrochloride, denatonium benzoate, or mixtures thereof. Any suitable level of aversive
agent may be used in the film. Suitable levels include, but are not limited to, 1
to 5000ppm, or even 100 to 2500ppm, or even 250 to 2000ppm.
[0084] Preferably, the water-soluble film or water-soluble unit dose article or both are
coated in a lubricating agent, preferably, wherein the lubricating agent is selected
from talc, zinc oxide, silicas, siloxanes, zeolites, silicic acid, alumina, sodium
sulphate, potassium sulphate, calcium carbonate, magnesium carbonate, sodium citrate,
sodium tripolyphosphate, potassium citrate, potassium tripolyphosphate, calcium stearate,
zinc stearate, magnesium stearate, starch, modified starches, clay, kaolin, gypsum,
cyclodextrins or mixtures thereof.
[0085] Preferably, the water-soluble film, and each individual component thereof, independently
comprises between Oppm and 20ppm, preferably between Oppm and 15ppm, more preferably
between Oppm and 10ppm, even more preferably between Oppm and 5ppm, even more preferably
between Oppm and 1ppm, even more preferably between Oppb and 100ppb, most preferably
Oppb dioxane. Those skilled in the art will be aware of known methods and techniques
to determine the dioxane level within water-soluble films and ingredients thereof.
Detergent ingredients
[0086] Suitable detergent ingredients can be described in terms of systems. The composition
typically comprises one or more of an alkalinity system, a bleach system, a builder
system, a chelant system, an enzyme system, a polymer system, and a surfactant system.
Suitable detergent ingredients can also include other detergent ingredients.
Alkalinity system.
[0087] The alkalinity system typically achieves the target pH profile of the composition.
The pH profile of the composition impacts the cleaning profile of the composition.
Alkalinity typically provides soil swelling and soil dispersion performance, as well
as providing the optimal pH for other detergent ingredients to work, such as the bleach
system, builder system, chelant system and enzyme system.
[0088] The composition typically comprises from 1.0g to 10g alkalinity system. The amount
of alkalinity system is typically determined by the desired pH profile of the composition.
[0089] The composition may comprise, by weight of the composition, from 10wt% to 35wt%,
or from 11wt% to 34wt%, or from 25wt% to 36wt%, or from 25wt% to 35wt% alkaline system.
[0090] The solid component may comprise, by weight of the solid component, from 10wt% to
35wt%, or from 11wt% to 34wt%, or from 25wt% to 36wt%, or from 25wt% to 35wt% alkaline
system.
[0091] Any suitable source of alkalinity can be used. Suitable sources of alkalinity are
organic alkaline ingredients and inorganic alkaline ingredients.
[0092] A suitable alkalinity system comprises ingredients selected from carbonate salts,
silicate salts, and sources of hydroxide anions.
[0093] The composition can comprise from 1.0g to 10g carbonate salt.
[0094] Preferred carbonate salts are selected from alkali metal salts of carbonate and/or
alkaline earth metal salts of carbonate. Preferred carbonate salts are selected from
magnesium carbonate, potassium carbonate, sodium carbonate, and any combination thereof,
most preferably sodium carbonate.
[0095] Preferably, the composition comprises from 1.0g to 10g sodium carbonate.
[0096] The composition can comprise from 0.1g to 5.0g silicate salt.
[0097] The composition may comprise, by weight of the composition, from 1.0wt% to 20wt%,
or from 1.0wt% to 17wt% silicate salt.
[0098] The solid component may comprise, by weight of the solid component, from 3.0wt% to
20wt%, or from 3.0wt% to 18wt% silicate salt.
[0099] The liquid component may comprise, by weight of the liquid component, from 20wt%
to 50wt% silicate salt.
[0100] Preferred silicate salts are selected from alkali metal salts of silicate and/or
alkaline earth metal salts of silicate. Preferred silicate salts are selected from
magnesium silicate, potassium silicate, sodium silicate, and any combination thereof,
most preferably sodium silicate. Preferred sodium silicates have a weight ratio SiO
2 to Na
2O ratio of from 1.0:1 to 3.5:1, preferably from 1.5:1 to 2.5:1, most preferably 2.0:1
(sodium disilicate).
[0101] Preferably, the composition comprises from 0.1g to 5.0g sodium silicate.
[0102] The composition may comprise from 0.01g to 2.0g source of hydroxide.
[0103] The composition may comprise, by weight of the composition, from 0.10wt% to 10wt%,
or from 0.10wt% to 8.0wt%, or from 0.1 1wt% to 6.7wt% source of hydroxide.
[0104] Preferred sources of hydroxide are selected from alkali metal hydroxide and/or alkaline
earth metal hydroxide. Preferred sources of hydroxide are selected from magnesium
hydroxide, potassium hydroxide, sodium hydroxide, and any combination thereof, most
preferably sodium hydroxide.
Bleach system.
[0105] Typically, the bleach system provides cleaning and disinfection benefits.
[0106] Typically, the composition comprises from 0.1g to 10g bleach system.
[0107] The composition may comprise, by weight of the composition, from 1.0wt% to 40wt%,
or from 1.0wt% to 35wt%, or from 1.0wt% to 33.7wt% bleach system.
[0108] The solid component may comprise, by weight of the solid component, from 2.5wt% to
35.7wt% bleach system.
[0109] The bleach system typically comprises a source of peroxygen, often in combination
with a bleach activator and/or a bleach catalyst.
[0110] Typically, the composition comprises from 0.1g to 10g, or from 1.0g to 8.0g, or from
2.0g to 6.0g source of peroxygen.
[0111] Any suitable source of peroxygen can be used. A suitable source of peroxygen is a
perhydrate salt, especially alkali metal perhydrate salts and/or alkaline earth metal
perhydrate salts, preferably alkali metal perhydrate salts. Suitable perhydrate salts
are selected from perborate salt, percarbonate salt, perphosphate salt, persilicate
salt, persulfate salt and any combination thereof.
[0112] The perhydrate salt may be a crystalline solid without additional protection. Alternatively,
the perhydrate salt can be coated. Suitable coatings are selected from sodium carbonate,
sodium silicate, sodium sulphate, and any combination thereof.
[0113] A preferred perhydrate salt is an alkali metal percarbonate, especially preferred
is sodium percarbonate. The percarbonate is preferably in a coated form. The coating
provides in-product stability.
[0114] The composition may comprise from 1.0g to 10g, or from 2.0g to 6.0g sodium percarbonate.
[0115] The composition may comprise, by weight of the composition, from 10wt% to 35wt%,
or from 11wt% to 34wt% sodium percarbonate.
[0116] The solid component may comprise, by weight of the solid component, from 25wt% to
40wt%, or from 25wt% to 36wt% sodium percarbonate.
[0117] Another suitable source of peroxygen is a pre-formed peracid. A preferred pre-formed
peracid is phthalimidoperoxycaproic acid (PAP).
[0118] The composition may comprise from 0.1g to 5.0g phthalimidoperoxycaproic acid (PAP).
[0119] The composition may comprise, by weight of the composition, from 1.0wt% to 20wt%,
or from 1.0wt% to 17wt% phthalimidoperoxycaproic acid (PAP).
[0120] The solid component may comprise, by weight of the solid component, from 2.5wt% to
20wt%, or from 2.5wt% to 18wt% phthalimidoperoxycaproic acid (PAP).
[0121] The composition may comprise a bleach activator. The composition may comprise from
0.05g to 2.0g, preferably from 0.1g to 2.0g, bleach activator.
[0122] The composition may comprise, by weight of the composition, from 0.5wt% to 10wt%,
or from 0.5wt% to 7.0wt% bleach activator.
[0123] Any suitable bleach activator can be used. Bleach activators are typically used to
enhance the bleaching performance at temperatures of 60°C and below.
[0124] A suitable bleach activator is an organic peracid precursor. Suitable bleach activators
are compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic
acids having preferably from 1 to 12 carbon atoms, in particular from 2 to 10 carbon
atoms, and/or optionally substituted perbenzoic acid. Suitable bleach activators comprise
O-acyl and/or N-acyl groups of the number of carbon atoms specified and/or optionally
substituted benzoyl groups. Preferred bleach activators are polyacylated alkylenediamines.
A highly preferred bleach activator is tetraacetylethylenediamine (TAED).
[0125] The composition may comprise from 0.05g to 2.0g, preferably from 0.1g to 2.0g, tetraacetylethylenediamine
(TAED).
[0126] The composition may comprise a bleach catalyst. The composition may comprise from
0.1mg to 20mg, preferably from 0.5mg to 10mg, bleach catalyst.
[0127] The composition may comprise, by weight of the composition, from 0.001wt% to 0.10wt%,
or from 0.001wt% to 0.07wt% bleach catalyst.
[0128] Any suitable bleach catalyst can be used.
[0129] Suitable bleach catalysts are metal-containing bleach catalysts, preferably transition-metal-containing
bleach catalysts. Preferred transition-metal-containing bleach catalysts are selected
from cobalt-containing bleach catalysts, iron-containing bleach catalysts, manganese-containing
bleach catalysts, and any combination thereof.
[0130] Suitable manganese-containing bleach catalysts comprise manganese in an oxidation
state of (II), (III), (IV), (v), or any combination thereof, preferably (IV).
[0131] Suitable manganese-containing bleach catalyst includes manganese triazacyclononane
and related complexes, such as 1,4,7-triazacyclononane (TACN).
[0132] The composition may comprise from 0.1mg to 20mg, preferably from 0.5mg to 10mg, transition-metal-containing
bleach catalyst. The composition may comprise from 0.1mg to 20mg, preferably from
0.5mg to 10mg, cobalt-containing bleach catalyst. The composition may comprise from
0.1mg to 20mg, preferably from 0.5mg to 10mg, iron-containing bleach catalyst. The
composition may comprise from 0.1mg to 20mg, preferably from 0.5mg to 10mg, manganese-containing
bleach catalyst.
Builder system
[0133] The composition may comprise from 1.0g to 10g builder system.
[0134] The composition may comprise, by weight of the composition, from 10wt% to 35wt%,
or from 1 1wt% to 34wt% builder system.
[0135] The solid component may comprise, by weight of the solid component, from 25wt% to
40wt%, or from 25wt% to 36wt% builder system.
[0136] The builder system typically comprises detergent ingredients that are complexing
agents. Suitable builder complexing agents are capable of sequestering hardness cations,
especially calcium cations and/or magnesium cations.
[0137] Typically, the builder system controls the hardness of the wash liquor, which in
turn aids the cleaning performance and soil suspension performance of the composition.
The builder system can also extract calcium and magnesium cations from the soil, which
also improves the cleaning performance of the composition.
[0138] Any suitable builder complexing agent can be used. Suitable builder complexing agents
may also be able to complex other cations, such as transition metal cations.
[0139] A preferred builder complexing agent is selected from aminopolycarboxylic acids and/or
salts thereof, carboxylic acids and/or salts thereof, and any combination thereof.
[0140] Suitable aminopolycarboxylic acids and/or salts thereof are selected from methylglycine-N,N-diacetic
acid and/or salts thereof (MGDA), glutamic acid diacetic acid and/or salts thereof
(GLDA), iminodisuccinic acid and/or salts thereof (IDS); hydroxyethyleiminodiacetic
acid and/or salts thereof (HEIDA), and any combination thereof, preferably methylglycine-N,N-diacetic
acid and/or salts thereof (MGDA) and/or glutamic acid diacetic acid and/or salts thereof
(GLDA), most preferably methylglycine-N,N-diacetic acid and/or salts thereof (MGDA).
A suitable builder complexing agent is the tri-sodium salt of methylglycine-N,N-diacetic
acid.
[0141] A suitable aminopolycarboxylic acid and/or salts thereof is ethylene diamine disuccinic
acid and/or salts thereof (EDDS).
[0142] Suitable carboxylic acids and/or salts thereof can be dicarboxylic acids and/or salts
thereof, such as glucaric acid and/or salts thereof, itaconic acid and/or salts thereof,
maleic acid and/or salts thereof, succinic acid and/or salts thereof, tartaric acid
and/or salts thereof, and any combination thereof.
[0143] Suitable carboxylic acids and/or salts thereof can be tricarboxylic acids and/or
salts thereof, A suitable carboxylic acid and/or salts thereof is citric acid and/or
salts thereof. A suitable builder complexing agent is sodium citrate.
[0144] The composition may comprise a builder complexing agent selected from methylglycine-N,N-diacetic
acid and/or salts thereof (MGDA) and/or citric acid and/or salts thereof. The composition
may comprise the combination of methylglycine-N,N-diacetic acid and/or salts thereof
(MGDA) and/or citric acid and/or salts thereof.
[0145] The composition may comprise from 1.0g to 10g methylglycine-N,N-diacetic acid and/or
salts thereof (MGDA). Any suitable methylglycine-N,N-diacetic acid and/or salt thereof
(MGDA) can be used. Preferably, the MGDA is the salt form of methylglycine-N,N-diacetic
acid, more preferably the MGDA is the tri-sodium salt of methylglycine-N,N-diacetic
acid.
[0146] The composition may comprise from 1.0g to 10g citric acid and/or salts thereof.
[0147] The presence of citric acid and/or salt thereof can be in conjunction with MGDA,
or independently thereof.
Chelant system
[0148] The composition may comprise from 0.1g to 5.0g chelant system.
[0149] The composition may comprise, by weight of the composition, from 1.0wt% to 20wt%,
or from 1.0wt% to 17wt% chelant system.
[0150] The solid component may comprise, by weight of the solid component, from 2.5wt% to
20wt%, or from 2.5wt% to 18wt% chelant system.
[0151] The chelant system typically comprising chelating agents. Suitable chelating agents
can chelate transition metal cations, especially copper, iron and zinc.
[0152] Typically, the chelant system stabilizes the bleaching system by protecting the bleach
from transition metal cation degradation. The chelant system can also extract transition
metal cations from soils, such as tea soils.
[0153] Any suitable chelating agent can be used. Suitable chelating agents may also be able
to complex other cations, such as hardness cations like calcium and magnesium.
[0154] Suitable chelating agents are selected from phosphonic acids and/or salts thereof.
Phosphonic acids and/or salts thereof typically provide crystal growth inhibition
performance.
[0155] A preferred phosphonic acid and/or salts thereof is selected from: 1-hydroxy ethylidene-1,1
diphosphonic acid and/or salts thereof (HEDP), amino trimethyl phosphonic acid and/or
salts thereof (ATMP), diethylene triamine pentamethylene phosphonic acid and/or salts
thereof (DTMP), 2- phosphono 1,2,4-butane tricarboxylic acid and/or salts thereof
(PBTC), and any combination thereof, preferably 1-hydroxy ethylidene-1,1 diphosphonic
acid and/or salts thereof (HEDP). A suitable chelating agent is the tetrasodium salt
of 1-hydroxy ethylidene-1,1 diphosphonic acid.
[0156] The composition may comprise from 0.1g to 5.0g chelating agent. The composition may
comprise from 0.1g to 1.5g 1-hydroxy ethylidene-1,1 diphosphonic acid and/or salts
thereof (HEDP).
[0157] The composition may comprise, by weight of the composition, from 1.0wt% to 5.0wt%
1-hydroxy ethylidene-1,1 diphosphonic acid and/or salts thereof (HEDP).
[0158] The solid component may comprise, by weight of the solid component, from 2.5wt% to
6.0wt%, or from 2.5wt% to 5.0wt% 1-hydroxy ethylidene-1,1 diphosphonic acid and/or
salts thereof (HEDP).
Enzyme system.
[0159] The composition may comprise from 1.0mg to 400mg enzyme system.
[0160] The enzyme system provides cleaning benefits.
[0161] The enzyme typically comprises an enzyme selected from amylase, cellulase, lipase,
protease and any combination thereof. Preferably, the enzyme system comprises an amylase
and/or a protease.
[0162] The composition typically comprises, on an active enzyme basis, from 1.0mg to300mg
of each enzyme type included in the composition.
[0163] The composition may comprise, by weight of the composition and on an active enzyme
basis, from 0.01wt% to 1.0wt% of each enzyme type included in the composition.
[0164] The solid component may comprise, by weight of the solid component and on an active
enzyme basis, from 0.03wt% to 1.07wt% of each enzyme type included in the solid component.
[0165] The composition may comprise, on an active enzyme basis, from 10.0mg to 300mg protease
and from 2.0mg to 30mg amylase.
[0166] The composition may comprise, by weight of the composition and on an active enzyme
basis, from 0.11wt% to 1,01wt% protease.
[0167] The solid component may comprise, by weight of the solid component and on an active
enzyme basis, from 0.25wt% to 1.07wt% protease.
[0168] The composition may comprise, by weight of the composition and on an active enzyme
basis, from 0.022wt% to 0.10wt% amylase.
[0169] The solid component may comprise, by weight of the solid component and on an active
enzyme basis, from 0.05wt% to 0.11wt% amylase.
[0170] Suitable enzymes can be in the form of granulates. Suitable enzyme granulates comprise
less than 29wt% of sodium sulphate. Suitable granulates comprise sodium sulphate in
an amount such that the weight ratio of the sodium sulphate and enzyme (on an active
enzyme basis) is less than 4:1.
[0171] In describing enzymes, the following nomenclature is used for ease of reference:
Original amino acid(s):position(s):substituted amino acid(s). Standard enzyme IUPAC
1-letter codes for amino acids are used.
Identity
[0172] Percent sequence "identity" means that a particular sequence has at least a certain
percentage of amino acid residues identical to those in a specified reference sequence,
when aligned using sofware programs such as the CLUSTAL W algorithm with default parameters.
See
Thompson et al. (1994) Nucleic Acids Res. 22:4673-4680. Default parameters for the CLUSTAL W algorithm are:
Gap opening penalty: |
10.0 |
Gap extension penalty: |
0.05 |
Protein weight matrix: |
BLOSUM series |
DNA weight matrix: |
IUB |
Delay divergent sequences %: |
40 |
Gap separation distance: |
8 |
DNA transitions weight: |
0.50 |
List hydrophilic residues: |
GPSNDQEKR |
Use negative matrix: |
OFF |
Toggle Residue specific penalties: |
ON |
Toggle hydrophilic penalties: |
ON |
Toggle end gap separation penalty |
OFF |
[0173] Deletions are counted as non-identical residues, compared to a reference sequence.
Amylase
[0174] Suitable amylases include alpha-amylases. Suitable amylases are from bacterial or
fungal origin.
[0175] A preferred alkaline alpha-amylase is derived from a strain of Bacillus, such as
Bacillus amyloliquefaciens, Bacillus licheniformis, Bacillus stearothermophilus, Bacillus
subtilis, or other Bacillus sp., such as Bacillus sp. 707, AA2560, DSM 9375, DSM 12368,
DSM 12649, DSM 12651, KSM AP1378, KSMK36, KSM K38, NCIB 12289, NCIB 12512 or NCIB
12513.
[0176] A preferred amylase is a variant of Bacillus sp. DSM12651. A preferred amylase is
a variant of Bacillus sp. DSM12651 amylase and has at least 90%, or at least 95%,
or even at least 99% identity to the Bacillus sp. DSM12651 amylase wildtype sequence.
[0177] A preferred amylase is a variant of Bacillus sp. DSM12651 amylase and has one or
more, or two or more, or three or more, or four or more, or five or more, or even
six or more mutations at the following positions:
1 , 2, 7, 9, 11, 16, 19, 25, 37, 43, 48, 54, 56, 58, 59, 60, 63, 81 , 84, 86, 90,
98, 104, 109, 111, 113, 116, 118, 125, 127, 130, 132, 133, 134, 135, 136, 139, 142,
144, 149, 158, 160, 163, 167, 169, 170, 171 , 172, 173, 174, 175, 176, 178, 181 ,182,
186, 187, 195, 202, 203, 204, 206, 209, 210, 212, T227, 235, 238, 246, 256, 259, 264,
265, 266, 267, 269, 270, 272, 273, 274, 275, 276, 284, 286, 291 , 293, 295, 298, 299,
302, 303, 304, 306, 310, 31 1 , 314, 315, 317, 319, 320, 323, 328, 337, 339, 345,
357, 365, 377, 375, 385, 391, 395, 400, 406, 408, 410, 431 , 435, 439, 444, 445, 458,
465, 466, 469, 473, 476, and 481.
[0178] A preferred amylase is a variant of Bacillus sp. DSM12651 amylase and has one or
more, or two or more, or three or more, or four or more, or five or more, or even
six or more mutations selected from the following mutations:
H1*; H2*, G7A; I9M; Q11 H; N16E; N16H; N16Y; N19D; N25K; N25M; N25T; A37V; W43Y; W48Y;
N54Q; N54S; V56I; V56T; Y58F; G59A; A60S; A60T; L63F; T81A; E84Q; E86L; R90H; R90N;
R90Q; Q98N; V104A; G109A; A1 11T; F113A; F1 13G; F113N; F113Q; F1 13T; F1 13Y; R116C;
R116D; R116F; R116H; R116K; R116N; R1 16S; R1 16Y; Q118N; Q118T; Q125G; Q125S; R127A;
R127F; R127H; R127L; R127N; R127T; E130D; E130F; E130I; E130K; E130L; E130N; E130S;
E130T; E130V; S132A; S132D; S132F; S132L; S132M; S132P; S132T; G133D; T134C; T134E;
T134N; T134P; T134R; T134S; T 134 W; T134Y; T134A; Y135H; Q136D; Q136E; Q136G; Q136N;
Q136R; Q136S; A139T; G142H; N144H; G149A; R158C; R158H; R158K; R158Q; R158S; Y160D;
Y160F; T160H; Y160N; D163H; W167*; Q169*; Q169E; Q169F; S170*; S170A; R171*; R171
H; R171 K; R171 L; R171Y; Q172*; Q172K; Q172N; Q172S; L173*; L173K; A174*; A174N;
A174S; N175*; N175S; R176*; R176A; Y178F; R181*; R181A; R181 C; R181 E; R181G; R181
H; R181 K; R181 N; R181 Q; G182*; G182T; A186D; A186E; A186H; A186K; A186N; A186T;
W187M; N195D; N195F; N195H; N195Q; N195Y; M202L; Y203L; A204V; V206L; D209N; H210K;
H210N; E212D; T227K; T227N; L235I; V238A; M246I; M246L; M246T; M246V; Q256H; Q256N;
K259G; K259H; V264A; V246I; V264T ; A265G; E266V; Y267F; Y267H; Y267L; K269M; K269Q;
K269R; N270G; N270P; L272I; G273V; A274K; A274S; L275A; L275I; L275V; E276N; W284R;
W284Y; M286L; V291A; V291 I; V291T; L293I; L293V; Y295F; Y298E; Y298N; Q299N; Q299Y;
N302A; N302H; N302K; N302Q; S303G; S304G; S304Q; N306H; N306K; N306Q; N306R; N306Y;
R310N; R310S; R310Q; N311 K; N311 R; N314Q; G315N; L317V; Q319H; R320K; R320Q; R320S;
S323T; H323K; F328L; G337D; G337E; A339S; Q345N; Q345R; L357F; Q365A; Q365C; Q365E;
Q365H; Q365K; Q365M; Q365S; P377K; P377T; D375H; D375N; D375Y; Q386L; K391A; Q395K;
R400S; D406H; W408H; V410I; S431F; G435C; W439R; W439T; R444T; Q445S; R458K; N465G;
Q466S; W469N; W469Y; F473I; F473P; F473S; G476K; and V481A.
[0179] A preferred amylase is a variant of Bacillus sp. DSM 12649 amylase. A preferred amylase
is a variant of Bacillus sp. DSM 12649 amylase and has at least 90%, or at least 95%,
or even at least 99% identity to the Bacillus sp. DSM 12649 amylase wildtype sequence.
[0180] A preferred amylase is a variant of Bacillus sp. DSM 12649 amylase and has one or
more, or two or more, or three or more, or four or more, or five or more, or even
six or more mutations at the following positions:
3, 6, 9, 10, 11, 26, 30, 33,37,82, 37, 106, 118, 128, 133, 149, 150, 160, 167, 178,
182, 186, 193, 195, 202, 203, 210, 214, 231, 232, 246, 256, 257, 258, 269, 270, 272,
283, 295, 296, 298, 299, 303, 304, 305, 311, 314, 315, 318, 319, 320, 323, 339, 345,
361, 366, 378, 383, 419, 421, 437, 441, 444, 445, 446, 447, 450, 458, 461, 471, 482,
and 484, preferably that also contain the deletions of 183* and/or 184*.
[0181] A preferred amylase is a variant of Bacillus sp. AA2560 amylase. A preferred amylase
is a variant of Bacillus sp. AA2560 amylase and has at least 90%, or at least 95%,
or even at least 99% identity to the Bacillus sp. AA2560 amylase wildtype sequence.
[0182] A preferred amylase is a variant of Bacillus sp. AA2560 amylase and has one or more,
or two or more, or three or more, or four or more, or five or more, or even six or
more mutations at the following positions:
6, 7, 40, 51, 91, 96, 98, 100, 116, 125, 172, 227, 229, 230, 231, 244, 262, 263, 281,
285, 286, 287, 288, 322, 323, 324, 325, 362, 363, and 364, and may preferably also
contain the deletions of D183 * and/or G184*.
[0183] A preferred amylase is a variant of Bacillus sp. AA2560 amylase and has the following
mutations:
A preferred amylase is Bacillus sp. SP707 amylase or a variant thereof. A preferred
amylase is Bacillus sp. SP707 amylase or a variant thereof, and has at least 90%,
or at least 95%, or even at least 99% identity to the Bacillus sp. SP707 amylase wildtype
sequence.
[0184] A preferred amylase is a variant of Bacillus sp. NCIB 12513 amylase. A preferred
amylase is a variant of Bacillus sp. NCIB 12513 amylase and has at least 90%, or at
least 95%, or even at least 99% identity to the Bacillus sp. NCIB12513 amylase wildtype
sequence.
[0185] A preferred amylase is a variant of Bacillus sp. NCIB12513 amylase and has one or
more, or two or more, or three or more, or four or more, or five or more, or even
six or more mutations at the following positions:
1, 7, 109, 140, 181, 182, 183, 184, 195, 206, 243, 260, 280, 284, 304, 320, 323, 391
and 476.
[0186] Suitable commercially available alpha-amylases include: KEMZYM
® (AT 9000 Biozym Biotech Trading GmbH Wehlistrasse 27b A-1200 Wien Austria); ENZYSIZE
®, OPTISIZE HT PLUS
®, PURASTAR
®, PURASTAR OXAM
®, and RAPIDASE
®, (Genencor International Inc., Palo Alto, California); KAM
® (Kao, 14-10 Nihonbashi Kayabacho, 1-chome, Chuo-ku Tokyo 103-8210, Japan); BAN
®, DURAMYL
®, FUNGAMYL
®, LIQUEZYME
®, NATALASE
®, POWERASE
®, STAINZYME
®, STAINZYME PLUS
®, SUPRAMYL
®, TERMAMYL
®, and TERMAMYL ULTRA
® (Novozymes A/S, Bagsvaerd, Denmark); and any combination thereof.
[0187] Preferred amylases include NATALASE
®, POWERASE
®, STAINZYME
®, STAINZYME PLUS
®, and any combination thereof.
Cellulase
[0188] Suitable cellulases include those of bacterial or fungal origin. Chemically modified
or protein engineered mutants are also suitable. Suitable cellulases include cellulases
from the genera Bacillus, Pseudomonas, Humicola, Fusarium, Thielavia, Acremonium,
e.g., the fungal cellulases produced from Humicola insolens, Fusarium oxysporum, and
Myceliophthora thermophila.
[0189] Commercially available cellulases include: Biotouch
® series of enzymes (AB Enzymes); Revitalenz
® series of enzymes (Du Pont); Carezyme
®, Carezyme
® Premium, Celluclean
®, Celluzyme
® and Whitezyme
® (Novozymes A/S); and any combination thereof.
[0190] Suitable commercially available cellulases include Celluclean
® Classic and/or Carezyme
® Premium.
Lipase
[0191] Suitable lipases include those of bacterial, fungal or synthetic origin, and variants
thereof. Chemically modified or protein engineered mutants are also suitable. Examples
of suitable lipases include lipases from Humicola (synonym Thermomyces), e.g., from
H. lanuginosa (T. lanuginosus).
[0192] A suitable lipase is a variant of the wild-type lipase from Thermomyces lanuginosus,
preferably comprising T231R and/or N233R mutations. Preferred lipases include those
sold under the tradenames Lipex
®, Lipoclean
®, and Lipolex
® by Novozymes, Bagsvaerd, Denmark.
[0193] Other suitable lipases include Liprl 139 and/or TfuLip2.
Protease
[0194] Suitable proteases include metalloproteases and serine proteases. Suitable proteases
include neutral or alkaline microbial serine proteases, such as subtilisins, as well
as chemically or genetically modified variants thereof.
[0195] Suitable proteases include proteases derived from Bacillus. Suitable proteases include
variants of: Bacillus alcalophilus, Bacillus amyloliquefaciens, Bacillus clausii,
Bacillus lentus, Bacillus gibsonii Bgi02446, Bacillus gibsonii DSM14391, Bacillus
pumilus, and Bacillus subtilis.
[0196] A preferred protease is a variant of Bacillus gibsonii protease. A preferred protease
is a variant of Bacillus gibsonii Bgi02446 protease or a variant of Bacillus gibsonii
DSM14391 protease.
[0197] A preferred protease is a variant of Bacillus gibsonii Bgi02446 protease. A preferred
protease is a variant of Bacillus gibsonii Bgi02446 protease and has at least 90%,
or at least 95%, or even at least 99% identity to the Bacillus gibsonii Bgi02446 protease
wildtype sequence.
[0198] A preferred protease is a variant of Bacillus gibsonii Bgi02446 protease and has
one or more, or two or more, or three or more, or four or more, or five or more, or
even six or more mutations at the following positions:
1, 3, 4, 8, 9, 10, 12, 14, 15, 16, 17, 18, 19, 20,21, 24, 25, 26, 33, 36, 37, 39,42,
43, 44, 47, 51, 52, 54, 55, 56, 57, 59, 60, 66, 69, 73, 74,76, 80, 82, 83, 84, 85,
86, 87,88, 89, 91, 95, 96, 97, 99, 101, 102, 104, 105, 106, 107, 108, 109, 110, 112,
113, 114, 115, 116, 118, 120, 122,124, 126, 127, 128, 129, 131, 133, 135 , 136, 137,
138, 139, 141, 142, 143, 144, 145, 147, 148, 150, 156, 157, 158, 159, 160, 161, 164,
166 , 167, 170, 174, 176, 177, 178, 179, 180, 182, 186, 188, 189, 190, 191, 192, 193,
198, 199, 200, 203, 207, 209, 210, 211, 212, 216, 218, 227, 228, 230, 231, 232, 234,
236, 238, 239, 242, 245, 246 , 247, 249, 250, 253, 254, 255, 256 , 257, 259, 262,
263, 264, 265, 266, 268, and 269.
[0199] A preferred protease is a variant of Bacillus gibsonii DSM14391 protease. A preferred
protease is a variant of Bacillus gibsonii DSM14391 protease and has at least 90%,
or at least 95%, or even at least 99% identity to the Bacillus gibsonii DSM14391 protease
wildtype sequence.
[0200] A preferred protease is a variant of Bacillus gibsonii DSM14391 protease and has
one or more, or two or more, or three or more, or four or more, or five or more, or
even six or more mutations at the following positions:
12, 43, 122, 127, 154, 156, 160, 211, 212, and 222.
[0201] A preferred protease is a variant of Bacillus alcalophilus protease. A preferred
protease is a variant of Bacillus alcalophilus protease and has at least 90%, or at
least 95%, or even at least 99% identity to the Bacillus alcalophilus protease wildtype
sequence.
[0202] A preferred protease is a variant of Bacillus alcalophilus protease and has one or
more, or two or more, or three or more, or four or more, or five or more, or even
six or more mutations at the following positions:
87, 99, 116, 118, 126, 127, 128, 129, and 130.
[0203] A preferred protease is a variant of Bacillus lentus protease. A preferred protease
is a variant of Bacillus lentus protease and has at least 90%, or at least 95%, or
even at least 99% identity to the Bacillus lentus protease wildtype sequence.
[0204] A preferred protease is a variant of Bacillus lentus protease and has one or more,
or two or more, or three or more, or four or more, or five or more, or even six or
more mutations at the following positions:
9, 15, 27, 66, 74, 76, 85, 99, 101, 103, 104, 116, 123, 126, 127, 128, 159, 212, 232,
236, 239, 245, 248, 252, and 274.
[0205] Suitable commercially available protease enzymes include those sold under the trade
names Savinase
®, Polarzyme
®, Kannase
®, Ovozyme
®, Everlase
® and Esperase
® by Novozymes A/S (Denmark), those sold under the tradename Properase
®, Purafect
®, Purafect Prime
®, Purafect Ox
®, FN3
®, FN4
®, Excellase
®, Ultimase
® and Purafect OXP
® by Genencor International, those sold under the tradename Opticlean
® and Optimase
® by Solvay Enzymes, those available from Henkel/ Kemira, namely BLAP, and any combination
thereof.
Other enzymes
[0206] Other suitable enzymes are bleaching enzymes. Preferred bleaching enzymes are peroxidases/oxidases.
Typical bleaching enzymes include those of plant, bacterial or fungal origin, and
variants thereof. Commercially available peroxidases include Guardzyme
® (Novozymes A/S).
[0207] Other suitable bleaching enzymes include choline oxidases and/or perhydrolases.
[0208] Suitable enzymes include sugar degrading enzymes. Suitable enzymes include glycosyl
hydrolase. A suitable enzyme is selected from glucanase, hemicellulase, mannanase,
xylanase, and any combination thereof.
[0209] Suitable mannanases are sold under the tradenames Mannastar
® (Du Pont) and
Mannaway
® (Novozymes A/S, Bagsvaerd, Denmark).
[0210] Suitable enzymes include pectate lyases. Suitable pectate lyases are sold under the
tradenames PrimaGreen
® (DuPont) and X-Pect
®, Pectaway
® (from Novozymes A/S, Bagsvaerd, Denmark).
[0211] A suitable enzyme is phospholipase.
Polymer system.
[0212] The composition may comprise from 0.1g to 5.0g, or from 0.5g to 2.0g polymer system.
[0213] The composition may comprise, by weight of the composition, from 1.0wt% to 20wt%,
or from 1.11wt% to 17wt% polymer system.
[0214] The liquid component may comprise, by weight of the liquid component, from 15wt%
to 60wt%, or from 20wt% to 50wt% polymer system.
[0215] The solid component may comprise, by weight of the solid component, from 2.5wt% to
20wt%, or from 2.5wt% to 18wt% polymer system.
[0216] The polymer system can act as soil dispersant as well, as a co-builder to help complex
hardness cations such as calcium and magnesium.
[0217] The polymer system typically comprises polymers. Suitable polymers are selected from
modified polyamine polymers, modified polysaccharide polymers, polyalkylene oxide
polymers, polycarboxylate polymers, silicone polymers, terephthalate polymers, other
polyester polymers, and any combination thereof.
[0218] Preferably, the polymer system comprises polymers selected from polyamine polymers,
modified polysaccharide polymers, polyalkylene oxide polymers, polycarboxylate polymers,
and any combination thereof, most preferably, polycarboxylate polymers.
[0219] The composition may comprise from 0.1g to 5.0g, or from 0.5g to 2.0g polycarboxylate
polymers.
Modified polyamine polymers
[0220] Suitable modified polyamine polymers comprise a polyamine core structure and a plurality
of alkoxylate groups attached to the core structure. The polyamine core structure
includes polyalkyleneimine, and linear or branched oligoamine.
[0221] The polyamine core structure and the alkoxylate groups attached to the core structure
can be further derivatized. For example, the polyamine core structure can be further
partly or completely quaternized with C
1-C
30 linear or branched alkyl, more preferably C
1-C
10 or even C
1-C
5 linear or branched alkyl, most preferably methyl. The alkoxylate group can be further
sulphated, sulphonated and/or substituted with an amino functional group.
[0222] Suitable modified polyamine dispersing agent includes ethoxylated polyethyleneimine
(EPEI). EPEI are effective dispersing agent for hydrophilic stains, especially hydrophilic
particulate stain such as clay.
[0223] Preferably, the EPEI comprises a polyethyleneimine backbone having weight average
molecular weight of between 100g/mol and 2000g/mol, preferably between 200g/mol and
1500g/mol, more preferably between 300g/mol and 1000g/mol, even more preferably between
400g/mol and 800g/mol, most preferably between 500g/mol and 700g/mol, preferably about
600. The ethoxylation chains within the EPEI may be from 200g/mol to 2000g/mol weight
average molecular weight, preferably from 400g/mol to 1500g/mol weight average molecular
weight, more preferably from 600g/mol to 1000g/mol weight average molecular weight,
most preferably about 880g/mol weight average molecular weight per ethoxylated chain.
The ethoxylation chains within the EPEI have on average 5 to 40, preferably 10 to
30, more preferably 15 to 25, even more preferably 18 to 22, most preferably about
20 ethoxy units per ethoxylation chain. The EPEI may have a total weight average molecular
weight of from 5000g/mol to 20000g/mol, preferably from 7500g/mol to 17500g/mol, more
preferably from 10000g/mol to 15000g/mol, even more preferably from 12000g/mol to
13000g/mol, most preferably about 12700g/mol. A preferred example is polyethyleneimine
core (with average molecular weight about 600g/mol) ethoxylated to 20 EO groups per
NH. Suitable EPEI this type includes Sokalan HP20 available from BASF, Lutensol FP620
from BASF. Examples of available polyethyleneimine ethoxylates also include those
prepared by reacting ethylene oxide with Epomine SP-006 manufactured by Nippon Shokubai.
[0224] The EPEI may comprise polyethyleneimine having an average molecular weight (Mw) ranging
from 1800 to 5000 g/mol (prior to ethoxylation), and the polyoxyethylene side chains
may have an average of from 25 to 40 ethoxy units per side chain bonded to the polyethyleneimine
backbone.
[0225] Suitable modified polyamine polymers include amphiphilic alkoxylated polyalkyleneimine
polymer. These polymers have balanced hydrophilic and hydrophobic properties such
that they remove grease and body soil particles from surfaces, and keep the particles
suspended in washing liquor. Suitable amphiphilic water-soluble alkoxylated polyalkyleneimine
polymers comprise polyalkyleneimine core, preferable polyethyleneimine core, and alkoxylate
group connected to the core. Suitable alkoxylate groups have the structure:
*-[A2-O]m-[CH2-CH2-O]n-[A3-O]p-R (V)
wherein:
"*" in each case denotes one-half of bond to the nitrogen atom of the core.
A2 is in each case independently selected from 1,2-propylene, 1,2-butylene, and 1,2-isobutylene.
A3 is 1,2-propylene.
R is in each case independently selected from hydrogen and C1-C4-alkyl, preferably hydrogen.
m has an average value in the range of from 0 to 2, preferably 0.
n has an average value in the range of 5 to 50.
p has an average value in the range of 3 to 50.
[0226] Suitable alkoxylated polyalkyleneimine polymers have a degree of quaterization ranging
from 0 to 50, preferably from 0 to 20, and more preferably from 0 to 10.
[0227] A preferred alkoxylated polyalkyleneimine polymer is polyethyleneimine (MW = 600)
modified with 24 ethoxylate groups per -NH and 16 propoxylate groups per -NH. Another
preferred alkoxylated polyalkyleneimine polymer is polyethyleneimine (MW = 600) modified
with 10 ethoxylate groups per -NH and 7 propoxylate groups per -NH.
[0228] Suitable alkoxylated polyalkyleneimine polymers include Sokalan HP30 Booster available
from BASF.
[0229] Suitable modified polyamine polymers includes zwitterionic polyamines. Suitable zwitterionic
polyamines have the structure:

wherein:
R is each independently C3-C20 linear or branched alkylene.
R1 is an anionic unit-capped polyalkyleneoxy unit having the formula: -(R2O)xR3.
R2 is C2-C4 linear or branched alkylene, preferably C2 (ethylene).
R3 is hydrogen, an anionic unit, and mixtures thereof, in which not all R3 groups are hydrogen, preferably wherein R3 anionic units are selected from -(CH2)pCO2M; -(CH2)qSO3M; - (CH2)qOSO3M; -(CH2)qCH(SO3M)-CH2SO3M; -(CH2)qCH(OSO3M)CH2OSO3M; - (CH2)qCH(SO3M)CH2SO3M; -(CH2)pPO3M; -PO3M ;-SO3M and mixtures thereof; wherein M is hydrogen or a water soluble cation, preferably
selected from sodium, potassium, ammonium, and mixtures thereof and in sufficient
amount to satisfy charge balance.
x is from 5 to 50, preferably from 10 to 40, even more preferably from 15 to 30, most
preferably from 20 to 25.
Q is a quaternizing unit selected from the group consisting of C1-C30 linear or branched alkyl, C6-C30 cycloalkyl, C7-C30 substituted or unsubstituted alkylenearyl, and mixtures thereof, preferably C1-C30 linear or branched alkyl, even more preferably C1-C10 or even C1-C5 linear or branched alkyl, most preferably methyl; the degree of quaternization preferably
is more than 50%, more preferably more than 70%, even more preferably more than 90%,
most preferably about 100.
X- is an anion present in sufficient amount to provide electronic neutrality, preferably
a water-soluble anion selected from the group consisting of chlorine, bromine, iodine,
methyl sulfate, and mixtures thereof, more preferably chloride.
n is from 0 to 8, preferably 0 to 4, preferably 0 to 2, most preferably 0.
[0230] A suitable zwitterionic polyamine having the following general structure: bis((C
2H
5O)(C
2H
4O)n)(CH
3)-N
+-C
xH
2x-N
+-(CH
3)-bis((C
2H
5O)(C
2H
4O)n), wherein n = from 20 to 30, and x = from 3 to 8, or sulphated or sulphonated
variants thereof.
[0231] A particular preferred zwitterionic polyamine is available from BASF as Lutensit
Z96 polymer (zwitterionic hexamethylene diamine according to below formula: 100% quaternized
and about 40% of the polyethoxy (EO
24) groups are sulfonated).

[0232] Another suitable zwitterionic polyamine is amphoterically-modified oligopropyleneimine
ethoxylates.
Modified polysaccharide polymers
[0233] Various polysaccharides can be useful as starting material for chemical modification
to make modified polysaccharide polymers, including cellulose, starch, guar, dextran,
polyglucan, chitin, curdlan, xylose, inulin, pullulan, locust bean gum, cassia gum,
tamarind gum (xyloglucan), xanthan gum, amylose, amylopectin, scleroglucan and any
combination thereof.
[0234] The most common type of modified polysaccharide is modified cellulose.
[0235] Modified cellulose polymers include anionic modified cellulose polymers which been
modified with functional groups that contain negative charge. Suitable anionic modified
cellulose polymers include carboxyalkyl cellulose, such as carboxymethyl cellulose.
The carboxymethyl cellulose may have a degree of carboxymethyl substitution of from
about 0.5 to about 0.9, and a molecular weight from about 80,000 Da to about 300,000
Da. Suitable carboxymethylcellulose include Finnfix
® series sold by CP Kelco or Nouryon, which include Finnfix
® GDA, a hydrophobically modified carboxymethylcellulose, e.g., the alkyl ketene dimer
derivative of carboxymethylcellulose sold under the tradename Finnfix
® SH1, or the blocky carboxymethylcellulose sold under the tradename Finnfix
®V. Other suitable anionic modified cellulose polymers include sulphoalkyl cellulose
and sulfoethyl cellulose.
[0236] Modified cellulose polymers also include nonionic modified cellulose polymers which
have been modified by a functional group that does not contain any charge. Suitable
nonionic modified cellulose polymers include alkyl cellulose, hydroxyalkyl cellulose,
hydroxyalkyl alkylcellulose, alkylalkoxyalkyl cellulose. Suitable nonionic modified
cellulose polymers also include nonionic cellulose carbamates, and nonionic 6-desoxy-6-amino-celluloses
derivative. Examples of alkyl cellulose include methyl cellulose (MC), ethyl cellulose
(EC), etc. Suitable ethyl celluloses are sold under tradename Ethocel
™ by Dow Chemicals, DuPont, or IFF. Examples of hydroxyalkyl celluloses include hydroxyethyl
cellulose (HEC) and hydroxypropyl cellulose (HPC). Suitable HECs are sold under tradename
Natrosol
™ hydroxyethylcellulose by Ashland, such as Natrosol
™ 250 with different grades available which have a total molar substitution (MS) of
2.5. Suitable HECs are also sold under tradename CELLOSIZE
™ Hydroxyethyl Cellulose by Dow Chemicals. Suitable HPCs are sold under tradename Klucel
™ by Ashland. Example of hydroxyalkyl alkylcellulose include hydroxypropyl methylcellulose
(HPMC), suitable HPMC are sold under tradename Methocel
™ with different grades available by Dow Chemicals, DuPont or IFF, and under tradename
Benecel
™ by Ashland.
[0237] Modified cellulose polymers also include cationic modified cellulose polymers which
been modified by functional group that contain cationic charge. Suitable cationic
modified celluloses include quaternized hydroxyethyl cellulose (Polyquaternium-10),
which is available under the tradename of Ucare by Dow Chemical, such as Ucare LR400,
Ucare LR30M, Ucare JR125, Ucare JR400, etc. Suitable cationic modified cellulose polymers
also include quaternized hydroxyethyl cellulose (HEC) polymers with cationic substitution
of trimethyl ammonium and dimethyldodecyl ammonium (Polyquaternium-67), which are
available under the tradename SoftCAT by Dow Chemical, such as SoftCAT SK, SoftCAT
SK-MH, SoftCAT SX, SoftCAT SL. Other suitable cationic modified celluloses include
those sold under tradename SupraCare
™ by Dow Chemical, such as SupraCare
™ 150, SupraCare
™ 133, SupraCare
™ 212. Suitable cationic modified cellulose polymers also include those modified with
cationic group and a hydrophobic group.
[0238] Another suitable type of modified polysaccharide is modified guar. The modified guar
can be nonionic modified, anionic modified, and/or cationic modified. Suitable nonionic
modified guar includes hydroxypropyl guar, such as N-Hance
™ HP40 and HP40S guar available from Ashland. Suitable example of modified guar also
include carboxymethyl hydroxypropyl guar (CMHPG) which is anionic and nonionic modified,
such as Galactasol
™ available from Ashland. Suitable modified guar also includes cationic modified guar,
such as guar hydroxypropyltrimonium chloride, which is available from by Ashland as
AquaCat
™ CG518 cationic solution, AquaCat
™ PF618 cationic solution, N-Hance
™ 3000, 3196, 3215, BF-13, BF-17, C261, C261N, CG13, CCG45. Other cationic modified
guar polymers are available from Solvay as Jaguar
® C 162, Excel, Excel SGI, Optima, C 13 S, C 13 SH, C14 S, C-17, LS SGI, C-500 STD.
Other nonionic and/or anionic modified guar include for example Jaguar
® HP 105 (Hydroxypropyl Guar gum), Jaguar
® SOFT and HP-120 COS (Carboxymethyl Hydroxypropyl Guar Gum).
[0239] Suitable modified polysaccharide polymers also include modified starch. Examples
of modified starch include carboxylate ester of starch, esterification product of
starch with e.g., C
6-C
24 alk(en)yl succinic anhydride;and starch maleates (starch react with maleic acid anhydride).
Examples of modified starch also include, but not limit to, acetylated starch, acetylated
distarch adipate, distarch phosphate, hydroxypropyl starch, hydroxy propyl distarch
phosphate, phosphated distarch ohosphate, acetylated distarch phosphate, starch sodium
octenyl succinate.
[0240] Suitable modified polysaccharide polymers also include polymers based on other polysaccharide,
such as cationic dextran polymers, the cationic dextran polymers are commercially
available under brand name CDC, CDC-L, CDC-H by Meito Sangyo.
[0241] Suitable modified polysaccharide polymers also include polymers based on polyglucans.
Suitable modified polyglucans are based on alpha 1,3-polyglucans and/or 1,6-polyglucans.
Preferably, the modified polyglucans can be cationic modified, such as cationic modified
alpha 1,3-polyglucan, such as cationic modified alpha 1,6-polyglucans. Another class
of preferred modified polyglucans can be hydrophobic and/or hydrophilic modified.
Polyglucan esters are especially preferred due to their performance and biodegradability
profiles.
[0242] Other suitable polysaccharide polymers include those based on inulin. Example of
modified inulin include carboxymethyl group modified inulin (CMI), suitable CMI are
Carboxyline series sold by Cosun Beet Company, including Carboxyline 25-40D, Carboxyline
25 D Powder, Carboxyline 20 LS D Powder, Carboxyline 25, Carboxyline 25-30 UP. Example
of modified inulin also include cationic modified inulin, suitable cationic modified
inulins include the Quatin series sold by Cosun Beet Company, including Quatin 350,
Quatin 380 and Quatin 1280 which are characterized by different degree of substitution
(DS), cationic density (meq/g) and molecular weight (g/mol).
[0243] Suitable modified polysaccharide polymers also include polymers based on other polysaccharide,
such as xylose carbamates, carboxy or sulfo-alkylated pullulan, carboxy- or sulfo-alkylated
chitosan, and any combination thereof.
Polyalkylene oxide polymers
[0244] Suitable polyalkylene oxide polymers include poly (ethylene oxide). Preferably the
poly (ethylene oxide) has a molecular weight from 1000 to 10000, more preferably from
2000 to 9000, more preferably from 3000 to 8500, most preferably from 4000 to 8000
such as 5000, 6000, 7000.
[0245] Suitable polyalkylene oxide polymers include graft polymers. Suitable graft polymers
can be based on polyalkylene oxide Suitable polymers comprise polyalkylene oxide backbone
(A) as a graft base and polymeric sidechains (B) grafted thereon. The polymeric sidechains
(B) are obtainable by polymerization of at least one vinyl ester monomer. The polyalkylene
oxide backbone (A) is obtainable by polymerization of at least one monomers selected
from the group of ethylene oxide, 1 ,2-propylene oxide, 1 ,2-butylene oxide, 2,3-butylene
oxide, 1 ,2-pentene oxide or 2,3-pentene oxide. Such graft polymers are known as effective
soil suspension polymers for hydrophobic and hydrophilic stains, surfactant boosters,
and sometimes as dye transfer inhibitors.
[0246] Suitable graft polymers include amphiphilic graft co-polymer comprising polyethylene
glycol backbone (A) as a graft base, and at least one pendant sidechains (B) selected
from polyvinyl acetate, polyvinyl alcohol and mixtures thereof. A preferred graft
polymer of this type is Sokalan HP22 available from BASF.
[0247] Suitable graft polymers are amphiphilic graft polymers based on water-soluble polyalkylene
oxides (A) as a graft base and side chains formed by polymerization of a vinyl ester
component (B), said polymers typically having an average of < one graft site per 50
alkylene oxide units and mean molar masses M typically of from 3 000 to 100 000. One
specific preferred graft polymer of this type is polyvinyl acetate grafted polyethylene
oxide copolymer having a polyethylene oxide as graft base and multiple polyvinyl acetate
side chains. The molecular weight of the polyethylene oxide backbone is typically
about 6000 and the weight ratio of the polyethylene oxide to polyvinyl acetate is
typically about 40 to 60 and typically no more than 1 grafting point per 50 ethylene
oxide units. The most preferred polymer of this type is available from BASF as Sokalan
PG101.
[0248] Suitable graft polymers include graft polymers comprising a block copolymer backbone
(A) as a graft base, wherein said block copolymer backbone (A) is obtainable by polymerization
of at least two monomers selected from the group of ethylene oxide, 1 ,2-propylene
oxide, 1 ,2-butylene oxide, 2,3-butylene oxide, 1 ,2-pentene oxide or 2,3-pentene
oxide, wherein the number (x) of individual blocks within the block copolymer backbone
(A) is an integer, wherein x is typically from 2 to 10 and preferably 3 to 5, and
(B) polymeric sidechains grafted onto the block copolymer backbone, wherein said polymeric
sidechains (B) are obtainable by polymerization of at least one vinyl ester monomer.
These polymers have improved biodegradation profiles.
[0249] Suitable graft polymers include graft polymers comprising a polyalkylene oxide backbone
(A) which has a number average molecular weight of from about 1000 to about 20,000
Daltons and is based on ethylene oxide, propylene oxide, or butylene oxide; and side
chains derived from N-vinylpyrrolidone (B), and side chains derived from vinyl ester
(C) derived from a saturated monocarboxylic acid containing from 1 to 6 carbon atoms
and/or a methyl or ethyl ester of acrylic or methacrylic acid.
Polycarboxylate polymers
[0250] Polycarboxylate polymers typically comprise at least one carboxy group-containing
monomer. The carboxy group-containing monomers are typically selected from acrylic
acid, methacrylic acid, fumaric acid, maleic acid, itaconic acid, aconitic acid, mesaconic
acid, citraconic acid, methylenemalonic acid, salts thereof, anhydrides thereof, and
any combination thereof.
[0251] Suitable polycarboxylate polymers include polyacrylate homopolymer having a molecular
weight of from 4,000 Da to 9,000 Da, or from 6,000 Da to 9,000 Da. Other suitable
carboxylate polymers include copolymers of acrylic acid (and/or methacrylic acid)
and maleic acid having a molecular weight of from 50,000 Da to 120,000 Da, or from
60,000 Da to 80,000 Da. The polyacrylate homopolymer and copolymer of acrylic acid
(and/or methacrylic acid) and maleic acid are commercially available as Acusol 445
and 445N, Acusol 531, Acusol 463, Acusol 448, Acusol 460, Acusol 465, Acusol 497,
Acusol 490 from Dow Chemicals, and as Sokalan CP 5, Sokalan CP 7, Sokalan CP 45, and
Sokalan CP 12S from BASF.
[0252] Suitable polycarboxylate polymers also include polyitaconate homopolymers, such as
Itaconix
® DSP 2K
™ sold by Itaconix, and Amaze SP available from Nouryon.
[0253] Suitable polycarboxylate polymers also include co-polymers comprising carboxy group-containing
monomers and one or more sulfonate or sulfonic group-containing monomers. The sulfonate
or sulfonic group containing monomers are typically selected from 2-acrylamido-2-methyl-l-propanesulfonic
acid (AMPS), 2-methacrylamido-2-methyl-l-propanesulfonic acid, 3-methacrylamido-2-hydroxy-propanesulfonic
acid, allysulfonic acid, methallysulfonic acid, 3-allyloxy-2-hydroxy-1-propanesulfonic
acid, 2-methyl-2-propenen-l-sulfonic acid, styrenesulfonic acid, vinylsulfonic acid,
3-sulfopropyl acrylate, 3-sulfopropylmethacrylate, sulfomethylacrylamide, sulfomethylmethacrylamide
and water soluble salts thereof.
[0254] Suitable polymers may comprise maleic acid, acrylic acid, and 3-allyloxy-2-hydroxy-1-propanesulfonic
acid. Suitable polymers may comprise acrylic acid and 2-acrylamido-2-methylpropane
sulfonate, such as those sold under tradename Acusol 588 by Dow Chemicals, Sokalan
CP50 by BASF, Aquatreat AR-545, Versaflex 310 and Versaflex 310-37 by Nouryon.
[0255] Suitable polymers include poly(itaconic acid-co-AMPS) sodium salt, such as Itaconix
® TSI
™ 322 and Itaconix
® CHT
™ 122 available from Itaconix.
[0256] Suitable polymers also includes those comprising other structure units in addition
to the sulfonate or sulfonic group group-containing monomers and carboxy group-containing
monomers. Suitable additional monomers are ether bond-containing monomers represented
by formula (1) and (2) below:

wherein in Formula (1):
R0 represents a hydrogen atom or CH3 group.
R represents a CH2 group, CH2CH2 group or single bond.
x represents a number 0-50, preferably 0-20, more preferably 0-5 (provided x represents
a number 1-5 when R is a single bond).
R1 is a hydrogen atom or C1 to C20 organic group.
wherein in Formula (2):
R0 represents a hydrogen atom or CH3 group.
R represents a CH2 group, CH2CH2 group or single bond.
x represents a number 0-5.
R1 is a hydrogen atom or C1 to C20 organic group.
[0257] A specific preferred polymer comprises structure units derived from 1 to 49 wt% of
1-(allyloxy)-3-butoxypropan-2-ol, from 50 to 98 wt% acrylic acid or methacrylic acid,
and from 1 to 49 wt% of 3-allyloxy-2-hydroxy-1-propanesulfonic acid, and the has a
weight average molecular weight of from about 20,000 to about 60,000. a specific preferred
polymer of this type comprises structure units derived from 1 to 10 wt% of 1-(allyloxy)-3-butoxypropan-2-ol,
from 70 to 89 wt% acrylic acid or methacrylic acid, and from 10 to 20 wt% of 3-allyloxy-2-hydroxy-1-propanesulfonic
acid, and the has a weight average molecular weight of from about 30,000 to about
60,000. Herein, 1-(allyloxy)-3-butoxypropan-2-ol is a preferred monomer as represented
by formula (2) when R
0 is H, R is CH
2, x is 0, and R
1 is n-butyl (C
4-alkyl).
[0258] Suitable polycarboxylate polymers also include co-polymers comprising carboxy group-containing
monomers and other suitable monomers. Other suitable monomers are selected from esters
and/or amide of the carboxy group-containing monomers, such as C
1-C
20 alkyl ester of acrylic acid; alkylene; vinyl ethers, such as methyl vinyl ether,
styrene and any mixtures thereof. One specific preferred polymer family of this type
is sold under tradename Gantrez by Ashland, which includes Gantrez An (alternating
co-polymer of methyl vinyl ether and maleic anhydride), Gantrez S (alternating co-polymer
of methyl vinyl ether and maleic acid), Gantrez ES (alternating co-polymer of methyl
vinyl ether and maleic acid ester), Gantrez MS (alternating co-polymer of methyl vinyl
ether and maleic acid salt).
[0259] Suitable polycarboxylate polymers also include polyepoxy succinic acid polymers (PESA).
A most preferred polyepoxy succinic acid polymer can be identified using CAS number:
51274-37-4, or 109578-44-1. Suitable polyepoxy succinic acid polymers are commercially
available from various suppliers, such as Aquapharm Chemicals Pvt. Ltd (commercial
name: Maxinol 600); Shandong Taihe Water Treatment Technologies Co., Ltd (commercial
name: PESA), and Sirius International (commercial name: Briteframe PESA).
[0260] Suitable polycarboxylate polymers may comprise a monomer having at least one aspartic
acid group or a salt thereof, this polymer comprises at least 25 mol%, 40 mol%, or
50 mol%, of said monomer. A preferabed example is sodium salt of poly(aspartic acid)
having a molecular weight of from 2000 to 3000 g/mol which is avilable as Baypure
® DS 100 from Lanxess. Suitable polyaspartates can be further modified.
Terephthalate polymers
[0261] Suitable terephthalate polymers are terephthalate-derived polyester polymers, which
comprise structure unit (I) and/or (II):
(I) -[(OCHR
1-CHR
2)
a-O-OC-Ar-CO-]
d
(II) -[(OCHR
3-CHR
4)
b-O-OC-sAr-CO-]
e
wherein:
a, b are from 1 to 200.
d, e are from 1 to 50.
Ar is independently selected from 1,4-substituted phenylene, and 1,3-substituted phenylene.
sAr is 1,3-substituted phenylene substituted in position 5 with -SO3M; wherein M is a counterion selected from Na, Li, K, Mg/2, Ca/2, Al/3, ammonium,
mono-, di-, tri-, or tetraalkylammonium wherein the alkyl groups are C1-C18 alkyl or C2-C10 hydroxyalkyl, or mixtures thereof.
R1, R2, R3, R4 are independently selected from H or C1-C18 n-alkyl or iso-alkyl; preferably selected from H or C1 alkyl.
[0262] Optionally, the polymer may further comprises one or more terminal group (III) derived
from polyalkylene glycolmonoalkylethers, preferably selected from structure (IV-a)
-O[C2H4-O]c-[C3H6-O]d-[C4H8-O]e-R7 (IV-a)
wherein:
R7 is a linear or branched C1-30 alkyl, C2-C30 alkenyl, or a cycloalkyl group with 5 to 9 carbon atoms, or a C8-C30 aryl group, or a C6-C30 arylalkyl group; preferably C1-4 alkyl, more preferably methyl.
c, d and e are, based on molar average, a number independently selected from 0 to
200, where the sum of c+d+e is from 2 to 500.
wherein the [C2H4-O], [C3H6-O] and [C4H8-O] groups of the terminal group (IV-a) may be arranged blockwise, alternating, periodically
and/or statistically, preferably blockwise and/or statistically, either of the [C2H4-O], [C3H6-O] and [C4H8-O] groups of the terminal group (IV-a) can be linked to -R7 and/or -O. Preferably, [C3H6-O] group is linked to -O, and the -O is further connected to -OC-Ar-CO- or -OC-sAr-CO-.
[0263] Optionally, the polymer may further comprise one or more anionic terminal unit (IV)
and/or (V) as described in
EP3222647. Where M is a counterion selected from Na
+, Li
+, K
+, ½ Mg
2+, ½ Ca
2+, 1/3 Al
3+, ammonium, mono-, di-, tri-, or tetraalkylammonium wherein the alkyl groups are C
1-C
18 alkyl or C
2-C
10 hydroxyalkyl, or mixtures thereof.
-O-CH2CH2-SO3M (IV)

[0264] Optionally, the polymer may comprise crosslinking multifunctional structural unit
which having at least three functional groups capable of the esterification reaction.
The functional which may be for example acid -, alcohol -, ester -, anhydride - or
epoxy groups, etc.
[0265] Optionally, other di- or polycarboxylic acids or their salts or their (di)alkylesters
can be used in the polyesters, such as, naphthalene-1,4-dicarboxylic acid, naphthalene-2,6,-dicarboxylic
acid, tetrahydrophthalic acid, trimellitic acid, diphenoxyethane-4,4'-dicarboxylic
acid, diphenyl-4,4'-dicarboxylic acid, 2,5-furandicarboxylic acid, adipic acid, sebacic
acid, decan-1,10-dicarboxylic acid, fumaric acid, succinic acid, 1,4-cyclohexanedicarboxylic
acid, cyclohexanediacetic acid, glutaric acid, azelaic acid, or their salts or their
(di)alkyl esters, preferably their (C
1-C
4)-(di)alkyl esters and more preferably their (di)methyl esters, or mixtures thereof.
[0266] One type of preferred polyester polymers are nonionic polyester polymers which do
not comprise the above structure unit (II). A particular preferred nonionic terephthalate-derived
polymer has a structure according to formula below:

wherein:
R5 and R6 are independently selected from H or CH3. More preferably, one of the R5 and R6 is H, and another is CH3.
c, d are, based on molar average, a number independently selected from 0 to 200, where
the sum of c+d is from 2 to 400.
More preferably, d is from 0 to 50, c is from 1 to 200.
More preferably, d is 1 to 10, c is 5 to 150.
R7 is C1-C4 alkyl and more preferably methyl.
N is, based on molar average, from 1 to 50.
[0267] One example of most preferred above suitable terephthalate-derived nonionic polymers
has one of the R
5 and R
6 is H, and another is CH
3; d is 0; c is from 5-100 and R
7 is methyl, and n is from 3-10.
[0268] Other suitable terephthalate-derived polyester polymers can be end capped. The end
capping group of these SRPs are typically selected from:
X-(OC
2H
4)
n-(OC
3H
6)
m-
wherein, X is C
1-C
4 alkyl and preferably methyl, the -(OC
2H
4) groups and the -(OC
3H
6) groups are arranged blockwise and the block consisting of the -(OC
3H
6) groups is bound to a COO group, n is based on a molar average a number of from 40
to 50, m is based on a molar average a number of from 1 to 10 and preferably of from
1 to 7.
[0269] The polyester may or may not be biodegradable, preferred soil release polymers are
readily biodegradable.
[0270] Example of suitable polyesters include TexCare
® series supplied by Clariant, including nonionic polymers Texcare
® SRN 100, SRN 170, SRN 170 C, SRN 170 Terra, SRN 172, SRN 240, SRN 260, SRN 260 life,
SRN 260 SG Terra, SRN UL50, SRN 300, SRN 325; and anionic polymers TexCare
® SRA 100, SRA 300, SRA300 F. Example of suitable polymers also include REPEL-O-TEX
® line of polymers supplied by Rhodia/Solvay, including the nonionic polymer REPEL-O-TEX
® Crystal, Crystal PLUS, Crystal NAT, SRP6; and the anionic polymer REPEL-O-TEX
® SF-2. Other examples of polymers includes the WeylClean
® series of polymers supplied by WeylChem, including nonionic polymers WeylClean
® PLN1, PLN2; and anionic polymers WeylClean
® PSA1. Other examples of polymers are Marloquest
® polymers, such as Marloquest
® SL, HSCB, L235M, U, B, and G82, supplied by Sasol. Suitable polymers include Sorez
100 (from ISP or Ashland).
Other polyester polymers
[0271] Suitable other polyester polymers include polyester soil release polymers derived
from bio-based 2,5-furandicarboxylic acid and derivatives thereof.
Surfactant system
[0272] Typically, the surfactant system provides cleaning benefits, shine benefits, water
drainage and drying benefits. The surfactant system can act to remove soil and suspend
soil.
[0273] The composition may comprise from 0.5g to 5.0g, or from 0.6g to 4.0g, or from 0.7g
to 3.0g surfactant system.
[0274] The composition may comprise, by weight of the composition, from 5.0wt% to 20wt%,
or from 5.5wt% to 17wt% surfactant system.
[0275] The liquid component may comprise, by weight of the liquid component, from 40wt%
to 100wt%, or from 50wt% to 100wt%, or from 50wt% to 99wt%, or from 50wt% to 90wt%
surfactant system.
[0276] The solid component may comprise, by weight of the solid component, from 10wt% to
20wt%, or from 12.5wt% to 18wt% surfactant system.
[0277] The surfactant system can comprise amphoteric surfactant, anionic surfactant, cationic
surfactant, nonionic surfactant, zwitterionic surfactant, and any combination thereof.
Most preferably, the surfactant system comprises nonionic surfactant.
[0278] The surfactant system typically comprises a surfactant, typically one or more, preferably
two or more, or three or more, or four or more, or even five or more different types
of surfactants, and preferably from 2 to 8, or 3 to 7, or 4 to 6 different types of
surfactants.
[0279] The surfactant system may have a phase inversion temperature, as measured at a concentration
of 1wt% in distilled water, between 20°C and 70°C, preferably between 35°C and 65°C.
Phase inversion temperature is the temperature below which a surfactant system partitions
preferentially into the water phase (typically as oil-swollen micelles), and above
which the surfactant system partitions preferentially into the oil phase (typically
as water swollen inverted micelles). Phase inversion temperature can be determined
visually by identifying at which temperature cloudiness occurs. The phase inversion
temperature of the surfactant system can be determined as follows: a solution containing
1wt% of the surfactant system, by weight of the solution in distilled water, is prepared.
The solution is stirred gently before phase inversion temperature analysis to ensure
that the process occurs in chemical equilibrium. The phase inversion temperature is
taken in a thermostable bath by immersing the solutions in 75 mm sealed glass test
tube. To ensure the absence of leakage, the test tube is weighed before and after
phase inversion temperature measurement. The temperature is gradually increased at
a rate of less than 1°C per minute, until the temperature reaches a few degrees below
the pre-estimated phase inversion temperature. Phase inversion temperature is determined
visually at the first sign of turbidity.
[0280] The surfactant system is typically a low foaming surfactant system.
Preferably, the surfactant system comprises a surfactant selected from:
- (i) R-O-EOx, wherein R is a C6-C18 alkyl, and x is from 1 to 30; or
- (ii) R-O-EOxPOy, wherein R is a C6-C18 alkyl, x is from 1 to 20, and y is from 1 to 20; or
- (iii) R-O-POxEOy, wherein R is a C6-C18 alkyl, x is from 1 to 20, and y is from 1 to 20; or
- (iv) R-O- EOxPOyEOz, wherein R is a C6-C18 alkyl, x is y from 1 to 20, y is from 1 to 20, and z is from 1 to 20; or
- (v) R-O- POxEOyPOz, wherein R is a C6-C18 alkyl, x is from 1 to 20, y is from 1 to 20, and z is from 1 to 20; or
- (vi) HO- EOxPOyEOz-H, wherein, x is from 1 to 50, y is from 1 to 50, and z is from 1 to 50; or
- (vii) HO- PxEOyPOz-H, wherein x is from 1 to 50, y is from 1 to 50, and z is from 1 to 20; or
- (viii) any combination thereof.
[0281] For the above surfactants (i) to (v) above, the alkyl moiety can be linear or branched,
and can be derived from a guerbet alcohol, or can derived from an oxo-alcohol.
[0282] Suitable surfactants are non-ionic surfactants.
[0283] A suitable surfactant has the formula: R-O-EO
x, wherein R is a C
6-C
18 alkyl, and x is from 1 to 30. Suitable surfactants are Lutensol AO series of surfactants
from BASF and Lutensol TO series of surfactants from BASF.
[0284] A suitable surfactant has the formula: R-O-EO
xPO
y, wherein R is a C
6-C
18 alkyl, x is from 1 to 20, and y is from 1 to 20. Suitable surfactants are Dehypon
LS series of surfactants from BASF.
[0285] A suitable surfactant has the formula: R-O-PO
yEO
x, wherein R is a C
6-C
18 alkyl, x is from 1 to 20, and y is from 1 to 20. Suitable surfactants are Ecosurf
EH series of surfactants from Dow.
[0286] A suitable surfactant has the formula: R-O- EO
xPO
yEO
x, wherein R is a C
6-C
18 alkyl, each x is independently from 1 to 20, and y is from 1 to 20. A suitable surfactant
is Plurafac LF403 from BASF.
[0287] A suitable surfactant has the formula: R-O- PO
yEO
xPO
y, wherein R is a C
6-C
18 alkyl, x is from 1 to 20, and each y is independently from 1 to 20. A suitable surfactant
is Plurafac SLF180 from BASF.
[0288] A suitable surfactant has the formula: HO- EO
xPO
yEO
x-H, wherein, each x is independently from 1 to 50, and y is from 1 to 50. Suitable
surfactants are the Pluronic PE series of surfactants from BASF, and the Tergitol
L series of surfactants from Dow.
[0289] A suitable surfactant has the formula: HO- PO
yEO
xPO
y-H, wherein x is from 1 to 50, and each y is independently from 1 to 50. Suitable
surfactants are the Pluronic RPE series of surfactants from BASF.
[0290] Other suitable surfactants include hydroxy mixed ether surfactants. The hydroxy mixed
ether surfactants can be modified and/or endcapped. Suitable hydroxy mixed ether surfactants
are Dehypon E127 and Dehypon GRA, both from BASF.
[0291] A suitable surfactant is amine oxide,
A suitable surfactant is betaine.
[0292] A suitable surfactant is an anionic surfactant selected from alkyl ether sulphates,
alkyl sulphates, alkyl sulphonates, and any combination thereof.
Other ingredients
[0293] Other suitable ingredients include aesthetic ingredients, fillers, glass care ingredients,
metal care ingredients, perfumes, solvents, suds control agents, and any combination
thereof.
[0294] Suitable fillers include sulphate salts. Suitable sulphate salts are alkali metal
salts of sulphate and/or alkaline earth metal salts of sulphate. Preferred sulphate
salts are selected from magnesium sulphate, sodium sulphate, and any combination thereof,
most preferably sodium sulphate.
[0295] Suitable glass care ingredients include zinc-containing compounds. Suitable zinc-containing
compounds include hydrozincite.
[0296] Suitable metal care ingredients include benzotriazole (BTA), tolyltriazole (TTA),
their salt-forms, and any combination thereof. Preferred salt-forms are sodium forms
of BTA and TTA.
[0297] Suitable solvents include alkanolamines, polyethers, polyols, and any combination
thereof.
[0298] Suitable alkanolamines are selected from monoethanolamine, diethanolamine, triethanolamine,
and any combination thereof.
[0299] Suitable polyethers are selected from glycerol ethers, polyethyleneglycol (PEG),
polypropyleneglycol (PPG), glycol ethers, and any combination thereof. Suitable glycol
ethers are the E-series and P-series of glycol ethers from Dow.
[0300] Suitable polyols are selected from propanediol, glycerol, sorbitol, and any combination
thereof.
[0301] The solvent can act as a process aid and/or a benefit agent.
EXAMPLES
[0302] The following is an illustrative example of an array in accordance with the present
invention.
|
g active |
|
First pouch |
Second pouch |
Third pouch |
# compartments enclosing solid component |
1 |
1 |
1 |
# compartments enclosing liquid component |
1 or 2 |
3 or 4 |
5 |
Solid Component |
trisodium salt of methylgylcine diacetic acid |
2.5 |
4 |
4 |
sodium citrate |
1 |
1 |
1.5 |
sodium carbonate |
4 |
2 |
2.5 |
sodium silicate |
0.2 |
0.5 |
0.6 |
sodium percarbonate |
1.5 |
3 |
3 |
1-hydroxyethane 1,1-diphosphonic acid |
0.6 |
1 |
0.7 |
sulphonated, carboxylated polymer |
1 |
0.4 |
0.8 |
tetraacetylethylenediamine |
0.3 |
0.4 |
0.5 |
metal bleach catalyst |
0.001 |
0.004 |
0.008 |
protease |
0.03 |
0.07 |
0.09 |
amylase |
0.006 |
0.01 |
0.01 |
processing aids (including fillers and perfume) |
1.5 |
2 |
2.5 |
TOTAL g |
12.637 |
14.384 |
16.208 |
Liquid Component |
alcohol alkoxylate |
0.43 |
0.8 |
1.6 |
polyalkylene oxide block copolymer |
0.43 |
0.8 |
1.6 |
processing aids (including water, dyes and solvents) |
0.2 |
0.8 |
1.2 |
TOTAL g |
1.06 |
2.4 |
4.4 |
|
|
|
|
Ratio liquid: solid |
0.08 |
0.17 |
0.27 |
[0303] The dimensions and values disclosed herein are not to be understood as being strictly
limited to the exact numerical values recited. Instead, unless otherwise specified,
each such dimension is intended to mean both the recited value and a functionally
equivalent range surrounding that value. For example, a dimension disclosed as "40
mm" is intended to mean "about 40 mm".