Technical Field and Background Art
[0001] The invention relates to aqueous high sudsing liquid detergent compositions containing
specified amounts and types of polymeric surfactants especially useful in the washing
of tableware, kitchenware and other hard surfaces.
[0002] Compositions incorporating polymeric surfactants are known in the art.
[0003] For example EP-A-0105556 discloses an aqueous liquid dishwashing detergent composition
containing a mixture of anionic, alkoxylated nonionic and alkyl polysaccharide surfactants
that provide enhanced drainage of rinse water from articles washed by the compositions.
Examples of suitable nonionic surfactants include the condensate of ethylene oxide,
propylene oxide and a compound containing hydroxyl or amine groups onto which the
alkylene oxides can be polymerised.
[0004] EP-A-0083223 also discloses detergent compositions incorporating alkylene oxide homo-
and co-polymers for grease and oil emulsification.
[0005] EP-A-0024711 discloses concentrated aqueous anionic surfactant solutions incorporating
the mono- and/or di-sulfates of poly C₂-C₃ alkylene glycols of MW >600 as viscosity
modifiers, optionally together with unsulfated C₂-C₃ polyalkylene glycols of MW >1500.
[0006] The compositions of this invention have superior ability to handle grease.
[0007] The performance of a detergent composition for cleaning tableware and kitchen utensils
is evaluated by its ability to handle grease. The detergent solution should readily
remove grease and minimize its redeposition.
[0008] There is continuing need for improved compositions and methods which can be employed
during dishwashing operations to improve the appearance of kitchen utensils and articles.
Such compositions and methods should provide improved removal of grease in conventional
dishwashing soil removal operations while maintaining the sudsing attributes of an
acceptable dishwashing detergent composition.
Summary of the Invention
[0009] According to the present invention there is provided a high sudsing liquid detergent
composition with enhanced grease handling ability containing by weight:
(a) from 5% to 50% anionic surfactant;
(b) from 0.1% to 10% of polymeric surfactant containing polymerised ethylene oxide
and/or propylene oxide groups, said polymeric surfactant having a molecular weight
of from 400 to 60,000;
(c) from 0% to 10% of a suds stabilizing nonionic surfactant selected from fatty acid
amides, trialkyl amine oxides and mixtures thereof;
(d) from 0% to 10% of a detergency builder selected from inorganic phosphates, inorganic
polyphosphates, inorganic silicates, inorganic carbonates, organic carboxylates, organic
phosphonates, and mixtures thereof;
(e) from 0% to 15% of an alkanol containing from one to six carbon atoms; and
(f) from 20% to 90% water,
characterised in that said polymeric surfactant is selected from compounds of formula
1) [R¹(R²O)
n(R³0)
m]
y[R⁴]
wherein R¹ is hydrogen, each R² or R³ is an alkylene group containing from two to
six carbon atoms with no more than 90% of said molecule comprising R² or R³ groups
containing two carbon atoms the (R₂O) and (R₃O) groups being interchangable; wherein
R⁴ is selected from
i) alkylene groups containing from one to 18 carbon atoms,
ii) poly (hydroxyalkylene oxide) groups wherein each alkylene group has from one to
six hydroxy groups and contains from three to eight carbon atoms and there are from
two to fifty hydroxy alkylene oxide groups and from two to fifty hydroxy groups,
iii) (=NR²N=), and
(iv) =N(̵R²NH)̵x,
wherein n is from 0 to 500, m is from 0 to 500, n+m is from 5 to 1000, x is from
2 to 50, and y is from 2 to 50 and equal to the available bonds of R⁴,
2) R¹(̵OCH₂CH₂)̵
xR²(̵OCH₂CH₂)̵
yOR¹
where: R¹ is H, CH₃, or CH₃(CH₂)
n where n is 1-17, or unsaturated analogues thereof, each of x and y is 2-500, and
R² is -O(CH₂)̵
z
where z = 1-18, or unsaturated analogues thereof, the percentage of (̵OCH₂CH₂)̵ groups
in the molecule being less than 90%;
wherein x is 8 and y is 4 or 14 or x is 17 and y is 10
wherein x is 7.5 or 16, and y is 2.75;
said composition having a pH of greater than six when the composition contains a C₁₀-C₂₀
alkylpolyethoxylate sulfate surfactant containing from 0.25 to 10 ethoxy groups per
molecule on average and having a viscosity of greater than 0.1 Pa.s, said composition
being substantially free of nonionic alkylpolyethoxylate detergent surfactant when
the amount of anionic surfactant is less than 20%, said anionic surfactant being a
C₁₀-C₂₀ alkyl polyethoxylate sulfate surfactant salt containing from 0.25 to 10 ethoxy
groups per molecule on the average when no magnesium ions or betaine surfactants are
present.
[0010] Dishware, glassware, and other tableware and kitchenware are washed in water solutions
of the detergent composition, generally at a weight concentration of from 0.05% to
0.4% of the composition in water at a temperature of from 15.6°C (60°F) to 48.9°C
(120°F).
Detailed Description of the Invention
[0011] The liquid detergent compositions of the present invention contain two essential
components:
(a) anionic surfactant which when there are no betaine surfactants or magnesium ions
present is a C₁₀-C₂₀ alkylpolyethoxylate sulfate containing an average of from 0.25
to 10 ethoxy groups per molecule, said average being computed herein by treating any
alkyl sulfate surfactant as an alkylpolyethoxylate sulfate containing 0 ethoxy groups,
to provide good sudsing, and preferably a low interfacial tension; and
(b) the polymeric surfactant, which improves grease handling.
[0012] Optional ingredients can be added to provide various performance and aesthetic characteristics.
Anionic Surfactant
[0013] The compositions of this invention contain from 5% to 50% by weight of an anionic
surfactant or mixtures thereof preferably comprising at least 5%, more preferably
at least 8%, and most preferably more than 10% of an alkyl polyethoxylate (polyethylene
oxide) sulfate having from 10 to 20, preferably from 10 to 16 carbon atoms in the
alkyl group and containing from
to 10, preferably from 1 to 8, most preferably from 1 to 6 ethoxy groups on the average.
Preferred compositions contain from 20% to 40% of anionic surfactant by weight.
[0014] Most anionic detergents can be broadly described as the water-soluble salts, particularly
the alkali metal, alkaline earth metal, ammonium or amine salts, of organic sulfuric
reaction products having in their molecular structure an alkyl radical containing
from 8 to 22 carbon atoms and a radical selected from the group consisting of sulfonic
acid and sulfuric acid ester radicals. Included in the term "alkyl" is the alkyl portion
of acyl radicals. Examples of the anionic synthetic detergents which can form the
surfactant component of the compositions of the present invention are the salts of
compatible cations, e.g. sodium, ammonium, monoethanolammonium, diethanolammonium,
triethanolammonium, potassium and/or, especially, magnesium cations with: alkyl sulfates,
especially those obtained by sulfating the higher alcohols (C₈-C₁₈ carbon atoms),
alkyl benzene, or alkyl toluene, sulfonates, in which the alkyl group contains from
9 to 15 carbon atoms, the alkyl radical being either a straight or branched aliphatic
chain; paraffin sulfonates or olefin sulfonates in which the alkyl or alkenyl group
contains from 10 to 20 carbon atoms; sodium C₁₀₋₂₀ alkyl glyceryl ether sulfonates,
especially those ethers of alcohols derived from tallow and coconut oil; coconut oil
fatty acid monoglyceride sulfates and sulfonates; alkylphenolpolyethylene oxide ether
sulfates with from 1 to 10 units of ethylene oxide per molecule on the average in
which the alkyl radicals contain from 8 to 12 carbon atoms; the reaction products
of fatty acids esterified with isethionic acid where, for example, the fatty acids
are derived from coconut oil; fatty acid amides of a methyl tauride in which the fatty
acids, for example, are derived from coconut oil; and beta-acetoxy- or beta-acetamido-alkanesulfonates
where the alkane has from 8 to 22 carbon atoms.
[0015] Specific examples of alkyl sulfate salts which can be employed in the instant detergent
compositions include sodium, potassium, ammonium, monoethanolammonium, diethanolammonium,
triethanolammonium, and magnesium: lauryl sulfates, stearyl sulfates, palmityl sulfates,
decyl sulfates, myristyl sulfates, tallow alkyl sulfates, coconut alkyl sulfates,
C₁₂₋₁₅ alkyl sulfates and mixtures of these surfactants. Preferred alkyl sulfates
include the C₁₂₋₁₅ alkyl sulfates.
[0016] Suitable alkylbenzene, or alkyltoluene, sulfonates include the alkali metal (lithium,
sodium, and/or potassium), alkaline earth (preferably magnesium), ammonium and for
alkanolammonium salts of straight, or branched-chain, alkylbenzene, or alkyltoluene,
sulfonic acids. Alkylbenzene sulfonic acids useful as precursors for these surfactants
include decyl benzene sulfonic acid, undecyl benzene sulfonic acid, dodecyl benzene
sulfonic acid, tridecyl benzene sulfonic acid, tetrapropylene benzene sulfonic acid
and mixtures thereof. Preferred sulfonic acids as precursors of the alkyl-benzene
sulfonates useful for compositions herein are those in which the alkyl chain is linear
and averages 11 to 13 carbon atoms in length.
[0017] The preferred anionic surfactants herein, which are essential if there are no, e.g.,
magnesium ions or betaine surfactant present, are alkylpolyethoxylate sulfates having
the formula RO(C₂H₄O)
xSO₃M wherein R is alkyl of from 10 to 20 carbon atoms, x is from 1/4 to ten on the
average, treating alkyl sulfates as if they had 0 ethoxy groups, preferably from
to eight, most preferably from one to six, and M is a water-soluble compatible cation
such as those disclosed hereinbefore. The alkylpolyethoxylate sulfates useful in the
present invention are sulfates of condensation products of ethylene oxide and monohydric
alcohols having from 10 to 20 carbon atoms. Preferably, R has 10 to 16 carbon atoms.
The alcohols can be derived from natural fats, e.g., coconut oil or tallow, or can
be synthetic. Such alcohols can be reacted with from
to 20, especially from one to 14, and more especially from one to eight, molar proportions
of ethylene oxide and the resulting mixture of molecular species is sulfated and neutralized.
[0018] There should be more than 10%, preferably more than 15% of such molecules containing
one to 10 ethoxylate groups calculated as a percentage of the total anionic surfactant
in the composition. When these molecules are mixed with alkyl sulfates which are treated
as containing 0 ethoxylate groups, the computed average degree of ethoxylation should
be more than 0.25, preferably more than 0.6. One can use a similar approach in computing
the minimum desired amount of the alkyl polyethoxylate sulfate which should be present
when admixed with any anionic surfactant. E.g. the other anionic surfactant can be
treated as if it were an alkyl sulfate to compute the average degree of ethoxylation.
[0019] Specific examples of alkylpolyethoxylate sulfates of the present invention are sodium
coconut alkylpolyethoxylate (3) ether sulfate, magnesium C₁₂₋₁₅ alkylpolyethoxylate
(3) ether sulfate, and sodium tallow alkylpolyethoxylate (6) ether sulfate. A particularly
preferred example is a water soluble, e.g. magnesium, C₁₂₋₁₃ alkylpolyethoxylate (1)
ether sulfate. Preferred alkyl polyethoxylate sulfates are those comprising a mixture
of individual compounds, said mixture having an average alkyl chain length of from
10 to 16 carbon atoms and an average degree of ethoxylation of from 1 to 8 moles of
ethylene oxide.
[0020] For use in completely soft water, the compositions should contain magnesium ions,
and/or at least 10%, preferably at least 15% by weight of the anionic surfactant,
of the preferred alkyl polyethoxylate sulfates described hereinbefore. It is preferred
that the compositions of this invention, including those that contain the preferred
alkylpolyethoxylate sulfates, also contain magnesium and/or calcium ions, most preferably
magnesium ions, to act as cations for a portion of the anionic surfactant. If the
composition is to be used primarily in water containing more than 0.17 ppm Ca++ of
hardness, added magnesium may not be essential. In use, from 10% to 100%, preferably
from 20% to 90%, of the anionic surfactant should be the magnesium salt.
[0021] The formulation of anionic surfactant systems that will reduce the interfacial tension
is well within the skill of the typical detergent formulator. For the purposes of
this invention, the surfactant system minus the polymeric surfactant should preferably
reduce the interfacial tension to below 0.25 Pa.cm, preferably below 0.2 Pa.cm , against
triolein at a concentration of 0.2% and a temperature of 115°F (46°C) in a spinning
drop Tensiometer. Interfacial tension is lowered by any detergent surfactant, but
the efficiency can be improved by selection of surfactants which have longer alkyl
chain lengths, use of cations such as magnesium which minimize charge effects when
anionic surfactants are used, and use of anionic surfactants combined with cosurfactants
like trialkylamine oxides which form complexes with the anionic surfactant. A more
complete discussion of such effects can be found in Milton J. Rosen, Surfactants and
Interfacial Phenomena, 149-173 (1978).
The Polymeric Surfactant
[0022] The compositions of the present invention contain from 0.1% to 10%, preferably from
1/2% to 4%, and most preferably from 1/2% to 2%, of the polymeric surfactant described
generically hereinbefore and discussed in detail hereinafter.
[0023] The polymeric surfactant can be a compound according to any one of the following
formulae:
1) [R¹(̵R²O)̵
n(̵R³O)̵
m]
y[R⁴]
wherein each R¹ is hydrogen, each R² or R³ is an alkylene group containing from two
to six carbon atoms with no more than 90% of said molecule comprising R² and R³ groups
containing two carbon atoms; wherein R⁴ is selected from alkylene groups containing
from one to 18 carbon atoms, polyhydroxyalkylene oxide groups wherein each alkylene
group has from one to six hydroxy groups and contains from three to eight carbon atoms
and there are from two to 50 hydroxyalkylene oxide groups and from two to about 50
hydroxy groups, (=NR²N=) and =N(̵R²NH)̵
x;
wherein n is from 0 to 500, m is from 0 to 500, n + m is from 5 to 1000, x is from
2 to 50, and y is from one to 50 and equal to the valences of R⁴; wherein the molecular
weight is from 400 to 60,000; and wherein the (R²O) and the (R³O) groups are interchangeable;
where: -
R¹ is H, or CH₃, or CH₃(CH₂)
n, or unsaturated analogues thereof
where:
n is 1-17
x,y is 2-500
R² is -O(CH₂)̵
z or unsaturated analogues of these where z is 1-18, the percentage of (̵OCH₂CH₂)̵
groups in the molecule being less than 90%;
where
X=8, Y=4
X=8, Y=14
X=17, Y=10
where
X=16, Y=2.75
X=7.5, Y=2.75
While not wishing to be bound by theory, it is believed that the polymeric surfactant
functions by forming complexes with the hydrophilic portions of the anionic surfactants,
thereby minimizing the ability of the anionic surfactants to leave a micelle or other
interfacial region once formed. Long terminal hydrocarbons pull the polymer into any
oil phase, thereby minimizing the number of anionic surfactant molecules that are
stabilized. Similarly, if the hydrophilic portion of the molecule is too hydrophilic,
the molecule is pulled into the aqueous phase too far. The molecule should be balanced
between hydrophobicity and hydrophilicity and have enough ether and/or amine linkages
spread throughout the structure to complex the anionic surfactant. The anionic surfactant
also must be one that will form the complex. Magnesium cations, ether linkages, and
amine or ammonium groups form stable complexes with the polymeric surfactants.
[0024] Preferably the surfactant contains a hydrophilic group comprising polyethylene oxide
and/or ethyleneimine groups containing from 1 to 500 ethylene oxide and/or ethyleneimine
derived moieties. The polymeric surfactant also contains at least one hydrophobic
group, preferably comprising polyalkylene oxide groups wherein the alkylene contains
from three to six, most preferably three, carbon atoms and the molecular weight is
from 400 to 60,000. The alkylene groups containing from 7 to 18, preferably from 10
to 18, carbon atoms can also be used, abut preferably only short chain relatively
nonoleophilic alkyl or acyl groups containing less than ten carbon atoms are pendant
on the polymeric surfactant.
[0025] Preferred surfactants are block copolymers comprising one or more groups that are
hydrophilic and which contain mostly ethylene oxide groups and one or more hydrophobic
groups which contain mostly propylene oxide groups attached to the residue of a compound
that contained one or more hydroxy or amine groups onto which the respective alkylene
oxides were polymerized, said polymers having molecular weights of from 400 to 60,000,
an ethylene oxide content of from 10% to 90% by weight and a propylene oxide content
of from 10% to 90% by weight.
[0026] Preferred surfactants are those in which propylene oxide is condensed with an amine,
especially ethylenediamine to provide a hydrophobic base having a molecular weight
of from 350 to 55,000, preferably from 500 to 40,000. This hydrophobic base is then
condensed with ethylene oxide to provide from 10% to 90%, preferably from 20% to 80%
ethylene oxide. Reverse structures in which the ethylene oxide is condensed first
are also desirable. These structures are especially easy to formulate into desirable
single phase liquid compositions.
[0027] Similar structures in which the ethylediamine is replaced by a polyol, especially
propylene glycol, or glycerine, or condensation products of glycerine, are also desirable.
[0028] In similar compositions, the polypropylene glycol portion can be replaced by an alkyl,
or alkylene group containing from 5 to 18, preferably from 8 to 16 carbon atoms.
Suds Stabilizing Nonionic Surfactant
[0029] The compositions of this invention contain from 0% to 10%, preferably from 1% to
8%, of suds stabilizing nonionic surfactant or mixtures thereof.
[0030] Suds stabilizing nonionic surfactants operable in the instant compositions are of
two basic types: fatty acid amides and the trialkyl amine oxide semi-polar nonionics.
[0031] The amide type of nonionic surface active agent includes the ammonia, monoethanol
and diethanol amides of fatty acids having an acyl moiety of from 8 to 18 carbon atoms
and represented by the general formula:
R¹-CO-N(H)
m(R²OH)
2-m
wherein R₁ is a saturated or unsaturated, aliphatic hydrocarbon radical having from
7 to 21, preferably from 11 to 17 carbon atoms; R² represents a methylene or ethylene
group; and m is 1 or 2. Specific examples of said amides are coconut fatty acid monoethanol
amide and dodecyl fatty acid diethanol amide. These acyl moieties may be derived from
naturally occurring glycerides e.g., coconut oil, palm oil, soybean oil and tallow,
but can be derived synthetically, e.g., by the oxidation of petroleum, or hydrogenation
of carbon monoxide by the Fischer-Tropsch process. The monoethanol amides and diethanolamides
of C₁₂₋₁₄ fatty acids are preferred.
[0032] Amine oxide semi-polar nonionic surface active agents comprise compounds and mixtures
of compounds having the formula:
wherein R¹ is an alkyl, 2-hydroxyalkyl, 3-hydroxyalkyl, or 3-alkoxy-2-hydroxypropyl
radical in which the alkyl and alkoxy, respectively, contain from 8 to 18 carbon atoms,
R² and R³ are each a methyl, ethyl, propyl, isopropyl, 2-hydroxyethyl, 2-hydroxypropyl,
or 3-hydroxypropyl radical and n is from 0 to 10. Particularly preferred are amine
oxides of the formula:
wherein R¹ is a C₁₀₋₁₄ alkyl and R² and R³ are methyl or ethyl.
[0033] The preferred sudsing characteristics of the compositions of the invention are those
which will provide the user of the product with an indication of cleaning potential
in a dishwashing solution. Soils encountered in dishwashing act as suds depressants
and the presence or absence of suds from the surface of a dishwashing solution is
a convenient guide to product usage. Mixtures of anionic surfactants and suds stabilizing
nonionic surfactants are utilized in the compositions of the invention because of
their high sudsing characteristics, their suds stability in the presence of food soils
and their ability to indicate accurately an adequate level of product usage in the
presence of soil.
[0034] In preferred embodiments of the invention, the ratio of anionic surfactants to suds
stabilizing nonionic surfactants in the composition will be in a molar ratio of from
11:1 to 1:1, and more preferably from 8:1 to 3:1.
Other Optional Surfactants
[0035] The compositions of the invention can desirably contain optional surfactants, especially
ampholytic and/or zwitterionic surfactants. However, when the level of anionic surfactant
is less than 20%, the composition should not contain any substantial amount of conventional
nonionic surfactant, e.g., an alkylpolyethoxylate, in addition to the polymeric surfactant.
Large amounts of conventional nonionic surfactants, e.g., more than about three or
four percent, tend to harm the sudsing ability of the composition.
[0036] When larger amounts ( > 20%) of anionic surfactants are present it is sometimes desirable
to have a low level, up to 5%, of conventional nonionic surfactants; "conventional"
nonionic surfactants are, e.g., C₈₋₁₈ alkyl polyethoxylates (4-15) or C₈₋₁₅ alkyl
phenol polyethoxylates (4-15).
[0037] Ampholytlc surfactants can be broadly described as derivatives of aliphatic amines
which contain a long chain of 8 to 18 carbon atoms and an anionic water-solubilizing
group, e.g. carboxylate, sulfonate or sulfate. Examples of compounds falling within
this definition are sodium-3-dodecylamino propane sulfonate, and dodecyl dimethylammonium
hexanoate.
[0038] Zwitterionic surface active agents operable in the instant composition are broadly
described as internally-neutralized derivatives of aliphatic quaternary ammonium and
phosphonium, and tertiary sulfonium compounds in which the aliphatic radical can be
straight chain or branched, and wherein one of the aliphatic substituents contains
from 8 to 18 carbon atoms and one contains an anionic water solubilizing group, e.g.,
carboxy, sulfo, sulfato, phosphato, or phosphono.
[0039] Highly preferred are betaine detergent surfactants which synergistically interact
with the polymeric surfactant to provide improved grease handling.
The Betaine Detergent Surfactant
[0040] The betaine detergent surfactant has the general formula:
wherein R is a hydrophobic group selected from alkyl groups containing from 10 to
22 carbon atoms, preferably from 12 to 18 carbon atoms, alkyl aryl and aryl alkyl
groups containing a similar number of carbon atoms with a benzene ring being treated
as equivalent to 2 carbon atoms, and similar structures interrupted by amido or ether
linkages; each R⁶ is an alkyl group containing from one to 3 carbon atoms; and R⁷
is an alkylene group containing from one to 6 carbon atoms.
[0041] Examples of preferred betaines are dodecylamidopropyl dimethylbetaine; dodecyldimethylbetaine;
tetradecyldimethylbetaine; cetyldimethylbetaine; cetylamidopropyldimethylbetaine,
tetradecyldimethylbetaine, tetradecylamidopropyldimethylbetaine, and docosyldimethylammonium
hexanoate and mixtures thereof.
[0042] Betaine surfactants are unique ingredients that provide exceptional benefits. When
betaine surfactant and polymeric surfactant are combined with any anionic surfactant
with, or without magnesium ions being present, superior grease holding benefits are
provided.
[0043] Betaines containing a C₁₂₋₁₄ alkyl provide a much bigger benefit when combined with
polymeric surfactant than when used by themselves.
[0044] The betaine is preferably present at a level of from
% to 15% by weight of the formula, preferably from 1% to 10%, most preferably from
1% to 8%. The ratio of anionic detergent surfactants to the betaine is from 1 to 80,
preferably from 1 to 40, more preferably from 2 to 40.
[0045] When betaines are present, the composition should preferably have a ratio of betaine
to polymeric surfactant of more than 7:1, preferably more than 9:1.
Solvents
[0046] Alcohols, such as ethyl alcohol, and hydrotropes, such as sodium and potassium toluene
sulfonate, sodium and potassium xylene sulfonate, trisodium sulfosuccinate and related
compounds (as disclosed in U.S. Patent 3,915,903), and urea, can be utilized in the
interests of achieving a desired product phase stability and viscosity. Alkanols containing
from one to six carbon atoms, especially two, and especially ethyl alcohol can be
present. Ethyl alcohol at a level of from 0% to 15%, preferably from 1% to 6%, and
potassium and/or sodium toluene, xylene, and/or cumene sulfonates at a level of from
1% to 6% can be used in the compositions of the invention. The viscosity should be
greater than 0.1 Pa.s, more preferably greater than 0.14 Pa.s, more preferably greater
than 0.2 Pa.s for consumer acceptance.
[0047] However the polymeric surfactant can be used to reduce the viscosity and provide
phase stability, e.g., when either the preferred alkyl polyethoxylate sulfate or magnesium
ions are present in the composition. For viscosity reduction, the percentage of ethylene
oxide in the polymer should be less than 70%, preferably less than 50%. Preferred
compositions contain less than 2% alcohol and less than 3% hydrotrope and preferably
essentially none while maintaining a viscosity of from 0.15 Pa.s to 0.5 Pa.s, preferably
from 0.2 Pa.s to 0.4 Pa.s. If viscosity reduction is not desired the percentage of
ethylene oxide in the polymer should be more than 50%, preferably more than 70%. The
polymeric surfactant reduces viscosity for all water soluble anionic surfactants.
[0048] The compositions of this invention contain from 20% to 90%, preferably from 30% to
80%, water.
Additional Optional Ingredients
[0049] The compositions of this invention can contain up to 10%, by weight of selected detergency
builders either of the organic or inorganic type. Examples of water-soluble inorganic
builders which can be used, alone or in admixture with themselves and organic alkaline
sequestrant builder salts, are alkali metal carbonates, phosphates, polyphosphates,
and silicates. Specific examples of such salts are sodium tripolyphosphate, sodium
carbonate, potassium carbonate, sodium pyrophosphate, potassium pyrophosphate, and
potassium tripolyphosphate. Examples of organic builder salts which can be used alone,
or in admixture with each other or with the preceding inorganic alkaline builder salts,
are alkali metal polycarboxylates, e.g., water-soluble citrates and tartrates, such
as sodium and potassium citrate and sodium and potassium tartrate. In general, however,
detergency builders have limited value in dishwashing detergent compositions and use
at levels above 10% can restrict formulation flexibility in liquid compositions because
of solubility and phase stability considerations. It is preferred that any builder
used be relatively specific to control of calcium as opposed to magnesium, Citrates,
tartrates, malates, maleates, succinates and malonates are especially preferred.
[0050] The detergent compositions of this invention can contain, if desired, any of the
usual adjuvants, diluents and additives, for example, perfumes, electrolytes, enzymes,
dyes, antitarnishing agents and antimicrobial agents, without detracting from the
advantageous properties of the compositions. Alkalinity sources and pH buffering agents
such as monoethanolamine, triethanolamine and alkali metal hydroxides can also be
utilized.
[0051] When the anionic surfactant is a C₁₀-C₂₀ alkylpolyethoxylate sulfate surfactant containing
from 0.25 to 10 ethoxy groups per molecule on average, the pH should be above 6, preferably
above 7 to avoid hydrolysis of the ester linkage. Also, it is desirable that the composition
be substantially free of antibacterial agents such as N-trichloromethyl-thio-4-cyclohexene-1,2,dicarboximide
for safety.
[0052] Low levels of antibacterial agents that will prevent growth of bacteria or molds
in the product, but which have essentially no effect in use can be desirable, especially
when low levels of alcohol are present.
[0053] All percentages and ratios herein are by weight unless otherwise indicated.
[0054] The following examples are given to illustrate the compositions of the invention.
[0055] In the following examples, the compounds have the following definitions. E stands
for an ethoxylate group and P stands for a propoxylate group.
Name |
Formula |
MW |
HLB |
Tetronic 504 |
(E₈P8.5)₄(=NCH₂CH₂N=) |
3400 |
15.5 |
Tetronic 702 |
(E4.5P₁₄)₄(=NCH₂CH₂N=) |
4000 |
7 |
Tetronic 704 |
(E12.5P₁₄)₄(=NCH₂CH₂N=) |
5500 |
15 |
Tetronic 707 |
(E47.5P₁₄)₄(=NCH₂CH₂N=) |
12000 |
27 |
Tetronic 902* |
(E₆P₁₇)₄(=NCH₂CH₂N=) |
5300 |
6.5 |
Tetronic 904* |
(E₁₇P₁₇)₄(=NCH₂CH₂N=) |
7500 |
14.5 |
Tetronic 907* |
(E₅₅P₁₇)₄(=NCH₂CH₂N=) |
13900 |
26 |
Tetronic 908 |
(E₉₁P₁₇)₄(=NCH₂CH₂N=) |
20000 |
30.5 |
Tetronic 1307 |
(E₇₄P₂₄)₄(=NCH₂CH₂N=) |
18600 |
23.5 |
Tetronic 1502* |
(E₁₀P₃₁)₄(=NCH₂CH₂N=) |
9000 |
5 |
Tetronic 1504 |
(E28.5P₃₁)₄(=NCH₂CH₂N=) |
12500 |
13 |
Tetronic 70R4 |
(P₁₄E12.5)₄(=NCH₂CH₂N=) |
5500 |
|
* Prepared by blending other commercially available materials. |
Tetronic is a Registered Trade Mark of the Union Carbide Co. |
[0056] The base product contains 5% magnesium C₁₂₋₁₃ alkyl sulfate, 23% mixed magnesium
and ammonium C₁₂₋₁₃ alkyl polyethoxylate (1) sulfate, 2.7% C₁₂₋₁₃ alkyl dimethyl amine
oxide; 5% ethyl alcohol, 3% sodium toluene sulfonate, about 60% water, and the balance
being inorganic salts and minor ingredients.
[0057] In the following examples, "grease cutting" is determined by the following test.
A preweighed 250 cc. polypropylene cup has 3 cc. of a melted beef grease applied to
its inner bottom surface. After the grease has solidified, the cup is reweighed. Then
a 0.4% aqueous solution of the composition to be tested is added to the cup to completely
fill it. The aqueous solution has a temperature of 46°C. After 15 minutes, the cup
is emptied and rinsed with distilled water. The cup is dried and then weighed to determine
the amount of grease removal. The amount removed by the base product is indexed at
100.
[0058] In the following examples, "grease capacity" is determined by modifying the above
grease cutting test by using 10 ml of an easier to remove fat which is an 80/20 mixture
of a solid vegetable shortening and a liquid vegetable shortening, lowering the detergent
concentration to about 0.2%, and soaking for 30 minutes to allow equilibrium to occur.
[0059] In the Examples "*" indicates a significant difference and the figures in parentheses
under the headings "Grease Capacity" and "Grease Cutting" are the number of replicates
run and averaged to give the indicated test scores.
[0060] In all of the Examples, the viscosity of the composition is greater than about 1.5
Pa.s and less than about 5 Pa.s centipoise.
EXAMPLE I
[0061] This test shows the improvement in grease capacity and grease cutting obtainable
with various Tetronics.
EXAMPLE II
[0062] This example demonstrates that reversing the order of addition of the ethylene oxide
and propylene oxide to create a hydrophilic center and hydrophobic ends provides compounds
which are equally as effective as the Tetronics.
EXAMPLE III
[0063] This example demonstrates that a polymeric surfactant with a somewhat hydrophilic
center, two or more intermediate hydrophobic moieties and terminal hydrophilic moieties
provides almost the same benefits as the Tetronics.
EXAMPLE IV
[0064] This example demonstrates that a compound with a hydrophilic chain with grafted polypropylene
oxide hydrophobic chains can provide grease capacity and grease cutting benefits in
accordance with the invention.
EXAMPLE V
[0065] This example shows that similar structures in which alkylene chains are substituted,
at least in part, for polypropoxylate moieties provide benefits in accordance with
the present invention.
COMPARATIVE EXAMPLE VI
[0066] This example demonstrates that mixtures of polypropylene glycol and polyethylene
glycol, and the individual materials do not provide the benefits.
COMPARATIVE EXAMPLE VII
[0067] This example demonstrates that excessively water-soluble compounds and compounds
which are more like conventional surfactants and contain terminal oleophilic hydrophobic
groups do not provide the benefits.
COMPARATIVE EXAMPLE VIII
[0068] This example is a continuation of Example VII.
COMPARATIVE EXAMPLE IX
[0069] This example also demonstrates that other conventional surfactants do not provide
the benefits.
EXAMPLE X
[0070] This example, shows the effect of increased Tetronic surfactant. Above 4%, there
is a loss which becomes substantial before a level of about 9% is reached.
COMPARATIVE EXAMPLE XI
[0071] This example shows the effect of using twice the amount of a commercial detergent.
The Grease Capacity and Grease Cutting are increased, but at a much greater cost than
associated with the invention.
|
Grease Capacity |
Grease Cutting |
Total |
Reps |
(4) |
(4) |
- |
Base Product |
100 |
100 |
200 |
Base Product (Double Usage) |
140* |
130* |
270* |
LSD₁₀ |
8 |
10 |
13 |
EXAMPLE XII
[0072] Viscosity Reduction
[0073] This example demonstrates the large reductions in viscosity obtained by adding the
polymeric surfactant. The viscosity can be adjusted back up by reducing alcohol and/or
hydrotrope levels. As can be seen, the higher the level of ethoxylate moieties in
the polymers, the less the reduction in viscosity.
Additional Materials Description
[0074] The additional polymeric surfactants not defined hereinbefore are as follows:
Name |
Formula |
MW |
HLB |
Tetronic 1302 |
(E₉ P₂₄)₄ (=NCH₂CH₂N=) |
7800 |
5.5 |
Tetronic 1304 |
(E₂₄ P₂₄)₄ (=NCH₂CH₂N=) |
10500 |
13.5 |
EXAMPLE XIII
[0075] In this example, a different type of test was used to demonstrate another aspect
of grease control by the detergent compositions. In most cases, this test gives a
ranking between formulations similar to that of the total index value of the preceeding
examples.
[0076] This test determines the effectiveness or strength of the grease emulsification by
the detergent by measuring the level of grease deposition on a hydrophobic surface
after its exposure to a detergent solution to which a grease has been added. This
test models the actual situation of redeposition of greases onto later washed items,
especially plastics.
[0077] For this experiment, 7.6 ℓ (2 gallons) of median hardness water [102.6 x 10⁻³ g/ℓ]
(6 grains/gallon) were held at 40.6°C (105°F), a common end-of-wash temperature for
dishwater. A 0.1% solution of the detergent product was made and mild agitation was
begun. Liquid vegetable oil was added in 6cc increments. At totals of 18cc, 36cc,
and 54cc, plastic items (3 for each grease level, 9 total) are dipped in succession
into the water. After drying , the mean weight gain per plastic item unit area is
calculated and indexed to a reference product.
[0078] The reference product used here is the base product. The polymeric surfactant is
added at the 1% level to the base.
[0079] A "*" indicates a statistically significant (LSD₀₅) reduction in grease redeposition
compared to the Base Product.
[0080] The compounds tested herein were those of formula 3.
in which, in compound,
- P
- X=8, Y=4
- Q
- X=8, Y=14
- R
- X=43, Y=4
- S
- X=43, Y=14
- T
- X=17, Y=10
and formula 4.
in which, in compound
U X=16, Y=2.75
V X=7.5, Y=2.75
[0081] Note from the above that Tetronic 704 and Compound F did not excel in this test,
but did perform well in the previous examples. Again, the Methocel® polymer does not
provide sufficient benefit.
[0082] Also, certain very high molecular weight compounds (R and S) do not show any advantage.
PREFERRED PROCESS
[0083] When some of the compositions of this invention are first made, they are not at equilibrium.
They typically require an aging period to reach equilibrium and exhibit the full benefit.
A period of about two weeks, which is about equivalent to the normal time between
making and use by the consumer is usually sufficient.
1. A high sudsing liquid detergent composition with enhanced grease handling ability
containing by weight:
(a) from 5% to 50% anionic surfactant;
(b) from 0.1% to 10% of polymeric surfactant containing polymerised ethylene oxide
and/or propylene oxide groups, said polymeric surfactant having a molecular weight
of from 400 to 60,000;
(c) from 0% to 10% of a suds stabilizing nonionic surfactant selected from fatty acid
amides, trialkyl amine oxides and mixtures thereof;
(d) from 0% to 10% of a detergency builder selected from inorganic phosphates, inorganic
polyphosphates, inorganic silicates, inorganic carbonates, organic carboxylates, organic
phosphonates, and mixtures thereof;
(e) from 0% to 15% of an alkanol containing from one to six carbon atoms; and
(f) from 20% to 90% water,
characterised in that said polymeric surfactant is selected from compounds of formula
1) [R¹(R²O)n(R³0)m]y[R⁴]
wherein R¹ is hydrogen, each R² or R³ is an alkylene group containing from two to
six carbon atoms with no more than 90% of said molecule comprising R² or R³ groups
containing two carbon atoms the (R₂O) and (R₃O) groups being interchangeable; wherein
R⁴ is selected from
i) alkylene groups containing from one to 18 carbon atoms,
ii) poly (hydroxyalkylene oxide) groups wherein each alkylene group has from one to
six hydroxy groups and contains from three to eight carbon atoms and there are from
to two fifty hydroxyalkylene oxide groups and from two to fifty hydroxy groups,
iii) (=NR²N=), and
(iv) =N (̵R²NH)̵x,
wherein n is from 0 to 500, m is from 0 to 500, n+m is from 5 to 1000, x is from
2 to 50, and y is from 2 to 50 and equal to the available bonds of R⁴,
2) R¹ (̵OCH₂CH₂)̵
xR²(̵OCH₂CH₂)̵
yOR¹
where: R¹ is H, CH₃, or CH₃(CH₂)
n where n is 1-17, or unsaturated analogues thereof, each of x and y is 2-500, and
R² is -O(CH₂)̵
z
where z = 1-18, or unsaturated analogues thereof, the percentage of (̵OCH₂CH₂)̵ groups
in the molecule being less than 90%;
wherein x is 8 and y is 4 or 14 or x is 17 and y is 10.
wherein x is 7.5 or 16, and y is 2.75;
said composition having a pH of greater than six when the composition contains a C₁₀-C₂₀
alkylpolyethoxylate sulfate surfactant containing from 0.25 to 10 ethoxy groups per
molecule on average and having a viscosity of greater than 0.1 Pa.s, said composition
being substantially free of nonionic alkylpolyethoxylate detergent surfactant when
the amount of anionic surfactant is less than 20%, said anionic surfactant being a
C₁₀-C₂₀ alkyl polyethoxylate sulfate surfactant salt containing from 0.25 to 10 ethoxy
groups per molecule on the average when no magnesium ions or betaine surfactants are
present.
2. A composition according to Claim 1 wherein there is from 0.1% to 7%, preferably from
0.5% to 4%, polymeric surfactant.
3. A composition according to either one of claims 1 & 2 wherein the anionic detergent
is selected from sodium, ammonium, monoethanolammonium, diethanolammonium, triethanolammonium,
potassium and magnesium salts of alkyl sulfates containing 8-18 carbon atoms, alkyl
benzene sulfonates in which the alkyl group contains form 9 to 15 carbon atoms, and
alkyl polyethoxylate sulfates in which the alkyl group contains from 10 to 20 carbon
atoms and there are from 0.5 to 10 ethoxylate groups on the average, and mixtures
thereof.
4. A composition according to any one of claims 1-3 wherein there is less than 2% polymeric
surfactant and in which from 10% to 100% of the anionic surfactant is in the form
of a magnesium salt.
5. A composition according to any one of claims 1-3 wherein there is at least 8% of an
alkylpolyethoxylate sulfate containing from 10 to 16 carbon atoms in the alkyl group
and from 0.5 to 8 ethoxylates on the average; wherein from 20% to 90% of the anionic
surfactant is the magnesium salt.
6. A composition according to any one of claims 1-4 wherein the anionic surfactant comprises
at least 10% alkylpolyethoxylate sulfate in which the alkyl group contains from 10
to 20 carbon atoms and containing from 1 to 6 ethoxylates on the average, alkyl sulfates
containing from 8 to 18 carbon atoms on the average, and mixtures thereof, and wherein
the suds stabilizing nonionic surfactant is an amine oxide semipolar nonionic surface
active agent comprising compounds having the formula:
wherein R¹ is an alkyl, 2-hydroxyalkyl, 3-hydroxyalkyl, or 3-alkoxy-2-hydroxypropyl
radical in which the alkyl and alkoxy groups, respectively, contain from 8 to 18 carbon
atoms, R² and R³ are each a methyl, ethyl, propyl, isopropyl, 2-hydroxyethyl, 2-hydroxypropyl,
or 3-hydroxypropyl radical and n is from 0 to 10.
7. A composition according to claim 4 when dependent on claim 3, wherein the anionic
surfactant is selected from mixtures of alkylbenzene sulfonates in which the alkyl
group contains from 9 to 15 carbon atoms and alkylpolyethoxylate sulfates in which
the alkyl group contains from 10 to 16 carbon atoms and there are from 0.5 to 6 ethoxylates
on the average and in which the suds stabilizing nonionic surfactant is a fatty acid
amide represented by the general formula:
R¹-CO-N(H)m(R²OH)2-m
wherein R₁ is a saturated or unsaturated, aliphatic hydrocarbon radical having from
7 to 21 carbon atoms, R² represents a methylene or ethylene group; and m is 1 or 2
and there is from 2% to 8% of said fatty acid amide.
8. A composition according to any one of claims 1-3 wherein there is from 0.5% to 4%
polymeric surfactant, in which surfactant the amount of ethylene oxide is less than
70% by weight, said composition containing less than 2% alkanol and less than 3% of
a hydrotrope material, and having a viscosity of from 0.15 to 0.5 Pa.s.
9. A composition according to claim 8 wherein there is less than 2% polymeric surfactant,
in which surfactant the amount of ethylene oxide in the polymeric surfactant is less
than 50% by weight, and wherein the viscosity is from 0.2 to 0.4 Pa.s.
1. Hochschäumende flüssige Detergenszusammensetzung mit erhöhter Fettbehandlungsfähigkeit,
enthaltend, bezogen auf das Gewicht:
(a) 5% bis 50% eines anionischen grenzflächenaktiven Mittels;
(b) 0,1% bis 10% eines polymeren grenzflächenaktiven Mittels, welches polymerisierte
Ethylenoxid- und/oder Propylenoxidgruppen enthält, welches polymere grenzflächenaktive
Mittel ein Molekulargewicht von 400 bis 60.000 aufweist;
(c) 0% bis 10% eines schaumstabilisierenden nichtionischen grenzflächenaktiven Mittels,
ausgewählt unter Fettsäureamiden, Trialkylaminoxiden und Gemischen hievon;
(d) 0% bis 10% eines Detergensgerüststoffes, ausgewählt unter anorganischen Phosphaten,
anorganischen Polyphosphaten, anorganischen Silicaten, anorganischen Carbonaten, organischen
Carboxylaten, organischen Phosphonaten und Gemischen hievon;
(e) 0% bis 15% eines Alkanols, welcher 1 bis 6 Kohlenstoffatome aufweist; und
(f) 20% bis 90% Wasser,
dadurch gekennzeichnet, daß das genannte polymere grenzflächenaktive Mittel unter
Verbindungen der Formel
1) [R¹(R²O)n(R³0)m]y[R⁴]
worin R¹ für Wasserstoff steht, jeder Rest R² oder R³ eine Alkylengruppe mit 2 bis
6 Kohlenstoffatomen ist, wobei nicht mehr als 90% des genannten Moleküls R²- oder
R³-Gruppen mit zwei Kohlenstoffatomen umfassen, worin die (R₂O)- und (R₃O)-Gruppen
untereinander austauschbar sind; worin R⁴ unter
i) Alkylengruppen mit 1 bis 18 Kohlenstoffatomen,
ii) Poly(hydroxyalkylenoxid)-Gruppen, worin jede Alkylengruppe 1 bis 6 Hydroxygruppen
aufweist und 3 bis 8 Kohlenstoffatome enthält, wobei 2 bis 50 Hydroxyalkylenoxidgruppen
und 2 bis 50 Hydroxygruppen vorhanden sind,
iii) (=NR²N=) und
iv) =N(̵R²NH)̵x ausgewählt ist,
worin n von 0 bis 500 beträgt, m von 0 bis 500 reicht, n+m von 5 bis 1000 beträgt,
x von 2 bis 50 reicht und y von 2 bis 50 beträgt und den verfügbaren Bindungen von
R⁴ entspricht;
2) R¹ (̵CH₂CH₂)̵
xR²(̵OCH₂CH₂)̵
yOR¹ ,
worin R¹ für H, CH₃ oder CH₃(CH₂)
n , worin n von 1 bis 17 beträgt, oder für nicht gesättigte Analoga hievon steht, x
und y beide von 2 bis 500 sind und R² -O(CH₂)̵
z , worin z von 1 bis 18 beträgt, oder ungesättigte Analoga hievon darstellt, wobei
der Prozentsatz von (̵OCH₂CH₂)̵-Gruppen im Molekül weniger als 90% beträgt;
worin x 8 ist und y 4 oder 14 beträgt oder x 17 ist und y 10 beträgt;
worin x 7,5 oder 16 ist und y 2,75 beträgt;
ausgewählt ist, welche Zusammensetzung einen pH-Wert von mehr als 6 aufweist, wenn
die Zusammensetzung ein C₁₀-C₂₀-Alkylpolyethoxylatsulfat-grenzflächenaktives Mittel
mit durchschnittlich 0,25 bis 10 Ethoxygruppen je Molekül enthält und eine Viskosität
von mehr als 0,1 Pa.s besitzt, welche Zusammensetzung im wesentlichen von nichtionischem
Alkylpolyethoxylat-grenzflächenaktivem Detergensmittel frei ist, wenn die Menge an
anionischem grenzflächenaktivem Mittel weniger als 20% beträgt, welches anionische
grenzflächenaktive Mittel ein C₁₀-C₂₀-Alkylpolyethoxylatsulfat-grenzflächenaktives
Salz mit durchschnittlich 0,25 bis 10 Ethoxygruppen je Molekül ist, wenn keine Magnesiumionen
oder Betain-grenzflächenaktive Mittel vorhanden sind.
2. Zusammensetzung nach Anspruch 1, worin 0,1% bis 7%, vorzugsweise 0,5% bis 4%, polymeres
grenzflächenaktives Mittel enthalten sind.
3. Zusammensetzung nach einem der Ansprüche 1 und 2, worin das anionische grenzflächenaktive
Detergensmittel unter Natrium-, Ammonium-, Monoethanolammonium-, Diethanolammonium-,
Triethanolammonium-, Kalium- und Magnesiumsalzen von Alkylsulfaten mit 8 bis 18 Kohlenstoffatomen,
Alkylbenzolsulfonaten, worin die Alkylgruppe 9 bis 15 Kohlenstoffatome aufweist, und
Alkylpolyethoxylatsulfaten, worin die Alkylgruppe von 10 bis 20 Kohlenstoffatome aufweist
und worin durchschnittlich 0,5 bis 10 Ethoxylatgruppen vorliegen, und unter Gemischen
hievon ausgewählt ist.
4. Zusammensetzung nach einem der Ansprüche 1 bis 3, worin weniger als 2% an polymerem
grenzflächenaktivem Mittel vorhanden sind, und worin 10% bis 100% des anionischen
grenzflächenaktiven Mittels in Form eines Magnesiumsalzes vorliegen.
5. Zusammensetzung nach einem der Ansprüche 1 bis 3, worin mindestens 8% eines Alkylpolyethoxylatsulfates
mit 10 bis 16 Kohlenstoffatomen in der Alkylgruppe und durchschnittlich 0,5 bis 8
Ethoxylatgruppen enthalten sind, wobei 20% bis 90% des anionischen grenzflächenaktiven
Mittels vom Magnesiumsalz gebildet werden.
6. Zusammensetzung nach einem der Ansprüche 1 bis 4, worin das anionische grenzflächenaktive
Mittel mindestens 10% Alkylpolyethoxylatsulfat, worin die Alkylgruppe 10 bis 20 Kohlenstoffatome
aufweist und welches durchschnittlich 1 bis 6 Ethoxylatgruppen besitzt, Alkylsulfate
mit durchschnittlich 8 bis 18 Kohlenstoffatomen und Gemische hievon umfaßt, und worin
das schaumstabilisierende nichtionische grenzflächenaktive Mittel ein semipolares
nichtionisches grenzflächenaktives Mittel auf Basis eines Aminoxides ist, welches
Verbindungen der Formel:
umfaßt, worin R¹ einen Alkyl-, 2-Hydroxyalkyl-, 3-Hydroxyalkyl- oder 3-Alkoxy-2-hydroxypropylrest
darstellt, worin die Alkyl- und Alkoxygruppen jeweils 8 bis 18 Kohlenstoffatome enthalten,
R² und R³ beide einen Methyl-, Ethyl-, Propyl-, Isopropyl-, 2-Hydroxyethyl-, 2-Hydroxypropyl-
oder 3-Hydroxypropylrest bedeuten und n von 0 bis 10 beträgt.
7. Zusammensetzung nach Anspruch 4, sofern sich dieser auf Anspruch 3 bezieht, worin
das anionische grenzflächenaktive Mittel unter Gemischen von Alkylbenzolsulfonaten,
worin die Alkylgruppe 9 bis 15 Kohlenstoffatome enthält, und Alkylpolyethoxylatsulfaten,
worin die Alkylgruppe 10 bis 16 Kohlenstoffatome enthält und welche durchschnittlich
0,5 bis 6 Ethoxylatgruppen aufweisen, ausgewählt ist und worin das schaumstabilisierende
nichtionische grenzflächenaktive Mittel ein Fettsäureamid ist, welches durch die allgemeine
Formel:
R¹-CO-N(H)m(R²OH)2-m
dargestellt ist, worin R¹ einen gesättigten oder ungesättigten aliphatischen Kohlenwasserstoffrest
mit 7 bis 21 Kohlenstoffatomen bedeutet, R² eine Methylen- oder Ethylengruppe darstellt
und m 1 oder 2 beträgt, und worin 2% bis 8% des genannten Fettsäureamides vorliegen.
8. Zusammensetzung nach einem der Ansprüche 1 bis 3, worin 0,5% bis 4% polymeres grenzflächenaktives
Mittel enthalten sind, in welchem grenzflächenaktivem Mittel die Menge an Ethylenoxid
weniger als 70 Gew.-% beträgt, welche Zusammensetzung mehr als 2% Alkanol und weniger
als 3% eines hydrotropen Materials beinhaltet und eine Viskosität von 0,15 bis 0,5
Pa.s aufweist.
9. Zusammensetzung nach Anspruch 8, worin weniger als 2% polymeres grenzflächenaktives
Mittel vorliegen, in welchem grenzflächenaktivem Mittel die Menge an Ethylenoxid im
polymeren grenzflächenaktiven Mittel weniger als 50 Gew.-% ist, und worin die Viskosität
0,2 bis 0,4 Pa.s beträgt.
1. Composition détergente liquide à fort pouvoir moussant ayant une capacité améliorée
de détachage des graisses, contenant, en poids :
(a) de 5% à 50% de tensioactif anionique;
(b) de 0,1 à 10% de tensioactif polymère contenant des groupes oxyde d'éthylène et/ou
oxyde de propylène polymérisés, ledit tensioactif polymère possédant une masse moléculaire
de 400 à 60 000;
(c) de 0% à 10% d'un tensioactif non ionique stabilisateur de mousse choisi parmi
les amides d'acides gras, les oxydes de trialkylamines et des mélanges de ceux-ci;
(d) de 0% à 10% d'un adjuvant de détergence choisi parmi les phosphates minéraux,
les polyphosphates minéraux, les silicates minéraux, les carbonates minéraux, les
carboxylates organiques, les phosphonates organiques, et des mélanges de ceux-ci;
(e) de 0% à 15% d'un alcanol contenant de 1 à 6 atomes de carbone; et
(f) de 20% à 90% d'eau,
caractérisée en ce que ledit tensioactif polymère est choisi parmi les composés de
formule
1) [R¹(R²O)n(R³O)m]y[R⁴]
dans laquelle R¹ est un hydrogène, chaque R² ou R³ est un groupe alkylène contenant
de 2 à 6 atomes de carbone, pas plus de 90% de ladite molécule comprenant des groupes
R² ou R³ contenant deux atomes de carbone, les groupes R²O et R³O étant interchangeables;
dans laquelle R⁴ est choisi parmi :
i) les groupes alkylène contenant de 1 à 18 atomes de carbone,
ii) les groupes poly(oxyde d'hydroxyalkylène) dans lesquels chaque groupe alkylène
possède de 1 à 6 groupes hydroxy et contient de 3 à 8 atomes de carbone et il existe
de 2 à 50 groupes oxyde d'hydroxyalkylène et de 2 à 50 groupes hydroxy,
iii) (-NR²N=), et
iv) =N-(R²NH)x-,
où n a une valeur de 0 à 500, m a une valeur de 0 à 500, n+m a une valeur de 5 à
1000, x a une valeur de 2 à 50, et y a une valeur de 2 à 50 et est égal aux liaisons
disponibles de R⁴;
2) R¹-(OCH₂CH₂)
x-R²-(OCH₂CH₂)
y-OR¹
dans laquelle R¹ est H, CH₃ ou CH₃(CH₂)
n, où n est 1-17, ou leurs analogues insaturés, chaque x et y a une valeur de 2-500
et R² est O(CH₂)
z-, où z a une valeur de 1-18, ou leurs analogues insaturés, le pourcentage de groupes
-(OCH₂CH₂)- dans la molécule étant inférieur à 90%;
dans laquelle x est égal à 8 et y est égal à 4 ou 14, ou x est égal à 17 et y est
égal à 10.
dans laquelle x est égal à 7,5 ou 16 et y est égal à 2,75;
ladite composition ayant un pH supérieur à 6 lorsque la composition contient un tensioactif
alkyl(en C₁₀-C₂₀)polyéthoxysulfate contenant en moyenne de 0,25 à 10 groupes éthoxy
par molécule et ayant une viscosité supérieure à 0,1 Pa.s, ladite composition étant
essentiellement dépourvue de tensioactif détergent alkylpolyéthoxylat non ionique
lorsque la quantité de tensioactif anionique est inférieure à 20%, ledit tensioactif
anionique étant un sel de tensioactif alkyl (en C₁₀-C₂₀)polyéthoxysulfate contenant
en moyenne de 0,25 à 10 groupes éthoxy par molécule en l'absence d'ions magnésium
ou de tensioactifs bétaïnes.
2. Composition selon la revendication 1, dans laquelle il y a de 0,1% à 7%, de préférence
de 0,5% à 4%, de tensioactif polymère.
3. Composition selon l'une quelconque des revendications 1 et 2, dans laquelle le détergent
anionique est choisi parmi les sels de sodium, d'ammonium, de monoéthanolammonium,
de diéthanolammonium, de triéthanolammonium, de potassium et de magnésium d'alkylsulfates
contenant 8-18 atomes de carbone, d'alkylbenzènesulfonates dans lesquels le groupe
alkyle contient de 9 à 15 atomes de carbone et d'alkylpolyéthoxysulfates dans lesquels
le groupe alkyle contient de 10 à 20 atomes de carbone et il y a en moyenne de 0,5
à 10 groupes éthoxylat, et des mélanges de ceux-ci.
4. Composition selon l'une quelconque des revendications 1-3, dans laquelle il y a moins
de 2% de tensioactif polymère et dans laquelle de 10% à 100% du tensioactif anionique
se trouve sous la forme d'un sel de magnésium.
5. Composition selon l'une quelconque des revendications 1-3, dans laquelle il y a au
moins 8% d'un akylpolyéthoxysulfate contenant de 10 à 16 atomes de carbone dans le
groupe alkyle et en moyenne de 0,5 à 8 groupes éthoxylat; dans laquelle de 20% à 90%
du tensioactif anionique est le sel de magnésium.
6. Composition selon l'une quelconque des revendications 1-4, dans laquelle le tensioactif
anionique comprend au moins 10% d'alkylpolyéthoxysulfate dans lequel le groupe alkyle
contient de 10 à 20 atomes de carbone et contenant en moyenne de 1 à 6 groupes éthoxylat,
d'alkylsulfates contenant en moyenne de 8 à 18 atomes de carbone, et des mélanges
de ceux-ci, et dans laquelle le tensioactif non ionique stabilisateur de mousse est
un agent tensioactif non ionique semipolaire de type oxyde d'amine comprenant des
composés répondant à la formule :
dans laquelle R¹ est un radical alkyle, 2-hydroxyalkyle, 3-hydroxyalkyle ou 3-alcoxy-2-hydroxypropyle
dans lequel les groupes alkyle et alcoxy contiennent respectivement de 8 à 18 atomes
de carbone, R² et R³ représentent chacun un radical méthyle, éthyle, propyle, isopropyle,
2-hydroxyéthyle, 2-hydroxypropyle ou 3-hydroxypropyle, et n a une valeur de 0 à 10.
7. Composition selon la revendication 4, lorsqu'elle dépend de la revendication 3, dans
laquelle le tensioactif anionique est choisi parmi les mélanges d'alkylbenzènesulfonates
dans lesquels le groupe alkyle contient de 9 à 15 atomes de carbone et d'alkylpolyéthoxysulfates
dans lesquels le groupe alkyle contient de 10 à 16 atomes de carbone et qui contiennent
en moyenne de 0,5 à 6 groupes éthoxylat, et dans laquelle le tensioactif non ionique
stabilisateur de mousse est un amide d'acide gras représenté par la formule générale
:
R¹-CO-N(H)m(R²OH)2-m
dans laquelle R¹ est un radical hydrocarboné aliphatique, saturé ou insaturé, de 7
à 21 atomes de carbone, R² représente un groupe méthylène ou éthylène; et m est égal
à 1 ou 2 et il y a de 2% à 8% dudit amide d'acide gras.
8. Composition selon l'une quelconque des revendications 1-3, dans laquelle il y a de
0,5% à 4% de tensioactif polymère, tensioactif dans lequel la quantité d'oxyde d'éthylène
est inférieure à 70% en poids, ladite composition contenant moins de 2% d'alcanol
et moins de 3% d'un produit hydrotrope et ayant une viscosité de 0,15 à 0,5 Pa.s.
9. Composition selon la revendication 8, dans laquelle il y a moins de 2% de tensioactif
polymère, tensioactif dans lequel la quantité d'oxyde d'éthylène dans le tensioactif
polymère est inférieure à 50% en poids, et dans laquelle la viscosité est de 0,2 à
0,4 Pa.s.