Technical Field
[0001] The invention relates to liquid dishwashing detergent compositions. The compositions
have antibacterial properties.
Background
[0002] Liquid dishwashing compositions are much desired by consumers and can be used neat
or diluted. In diluted mode, a composition is diluted in water to form a wash liquor
in which the dishes to be cleaned are immersed. In neat mode, a composition is directly
applied neat onto dishes, and in this mode a dish implement is often use. Specifically,
the composition is applied onto the implement, usually a sponge or a dishcloth, which
is in turn contacted with the dishes to be cleaned.
[0003] A problem arises that dish implements are left humid most of the time, and so they
provide a good medium for bacterial growth. The contaminated implement which is used
to clean dishes will in turn contaminate those dishes.
[0004] We have now found that certain dishwashing compositions can fulfill the further purpose
of reducing or eliminating bacterial growth on dish implements.
Summary of the Invention
[0005] The compositions of the present invention are liquid dishwashing compositions comprising
:
- a surfactant,
- a hydrotrope selected from the group consisting of salts of cumene sulfonate, toluene
sulfonate, xylene sulfonate, benzene sulfonate or mixtures thereof; and
- an unsaturated aliphatic terpene alcohol or derivative.
[0006] The invention further encompasses a method of washing dishes with these compositions.
Without wishing to be bound by theory, it is believed that the anti bacterial efficacy
of said formulations is mainly driven by a synergy between the hydrotrope(s) and the
unsaturated aliphatic terpene alcohol(s) or derivative.
Detailed Description of the Invention
[0007] The compositions of the invention are aqueous liquid compositions. They typically
comprise from 30% to 80% by weight of the total composition of water, preferably 40%
to 70%.
[0008] The compositions herein are liquid and so they typically have a viscosity of from
50 cps to 2000 cps, preferably 100 cps to 350 cps, measured with a Brookfield Viscometer,
with a No. 18 spindle, at 20°C.
Surfactants
[0009] The compositions of the present invention comprise, as an essential ingredient, one
or several of the following surfactants. Suitable for use herein are amine oxides
according to the formula :

wherein R
2 represents a straight or branched alkyl or alkenyl group having 10 to 16 carbon atoms,
and R
3 and R
4 represent a C
1 to C
4 hydrocarbon chain, preferably a methyl group or an ethyl group. Generally, when the
number of carbon atoms in R
2 is less than 10, the detergency of the composition is lowered, while if it exceeds
16, the stability of the composition at low temperatures deteriorates.
[0010] Also suitable for use herein are alkyl alkoxylated sulfates of the formula R
1O(A)
nSO
3M, wherein R
1 is an alkyl or alkenyl group having 9 to 15 carbon atoms, A is an alkoxy group, preferably
ethoxy or propoxy, most preferably ethoxy, n represents 0.5 to 7 of real number in
average, and M is an alkalimetal, alkali earth metal, ammonium or alkanolammonium
group.
[0011] The use of alkyl alkoxylated sulfates with lower values for n, on an equal weight
basis, typically when n is below 1.0, improves the performance of the composition
on grease removal and sudsing due to the corresponding increase in moles of anionic
but results in an increase in the total amount of unalkoxylated alkyl sulphate, and
this seems to make the low temperature instability issue more acute. If different
alkyl alkoxylated sulfates are used which have different n values, the resulting average
n value of the alkyl alkoxylated sulfate in the composition will be the weighted molar
average n value of the individual n values of the different alkyl alkoxylated sulfates
used in the composition.
[0012] If the average n value is less than 0.5, the stimulus to skin increases and this
is not desirable. On the other hand, if the average n value is more than 3, the detergency
deteriorates.
[0013] Concerning R
1, if the average number of carbon atoms in R
1 is less than 9, the detergency is insufficient, while if it is more than 16, the
stability at low temperature deteriorates.
[0014] Suitable alkyl alkoxylated material for use herein can be straight or branched materials.
By branched material, it is meant that R
1 is branched, while the position of the branching, and the length of the branched
group is as determined by the position of the CH2-OH functional group in the parent
alcohol. The increase in the proportion of branched material can improve the physical
stability of the composition at low temperature.
[0015] In this respect, it is important that the branched alkyl alkoxylated sulfate material
should not represent more than 60%, by weight, of the total alkyl alkoxylated sulfate
(branched plus linear), otherwise the sudsing performance of the product deteriorates
unacceptably. At the other end of the range, there should be enough branched alkyl
alkoxylated sulfate to achieve a suitable low temperature stability. This minimum
value depends on the specific needs, and can be evaluated by plotting the stability
of a given matrix at the desired temperature, as a function of the proportion of branched
material. Generally, branched alkyl alkoxylated sulfates should be present in amounts
of up to 60%, preferably from 10% to 55%, most preferably 20% to 50%.
[0016] Alkyl alkoxylated sulfates are commercially available with a variety of chain lengths,
degrees of alkoxylation and degrees of branching under the trade names Empicol® ESA
70 (AE1S) or Empicol® ESB 70 (AE2S) by Albright & Wilson, with C12/14 carbon chain
length distribution which are derived from natural alcohols and are 100% linear, Empimin®
KSL68/A - AE1S and Empimin® KSN70/LA - AE3S by Albright & Wilson with C12/13 chain
length distribution and about 60% branching, Dobanol® 23 ethoxylated sulphates from
Shell with C12/13 chain length distribution and about 18% branching, Lial® 123 ethoxylated
sulphates from Condea Augusta with C12/13 chain length distribution and about 60%
branching and Isalchem® 123 alkoxylated sulphates with C12/13 chain length distribution
and about 95% branching.
[0017] Also, suitable alkyl alkoxylated sulfates can be prepared by alkoxylating and sulfating
the appropriate alcohols, as described in "Surfactants in Consumer Products" by J.Falbe
and "Fatty oxo-alcohols : Relation between their alkyl chain structure and the performance
of the derived AE,AS,AES" submitted to the 4th World Surfactants, Barcelona, 3-7 VI
1996 Congress by Condea Augusta. Commercial oxo-alcohols are a mixture of primary
alcohols containing several isomers and homologues. Industrial processes allow one
to separate these isomers hence resulting in alcohols with linear isomer content ranging
from 5-10% to upto 95%. Examples of available alcohols for alkoxylation and sulfation
are Lial® alcohols by Condea Augusta (60% branched), Isalchem® alcohols by Condea
Augusta (95% branched), Dobanol® alcohols by Shell (18% linear).
[0018] Other suitable surfactants for use herein are :
- Alkyl benzene sulfonates in which the alkyl group contains from 9 to 15 carbon atoms,
preferably 11 to 40 carbon atoms in straight chain or branched chain configuration.
An especially preferred linear alkyl benzene sulfonate contains about 12 carbon atoms.
U.S. Pat. Nos. 2,220,099 and 2,477,383 describe these surfactants in detail.
- Alkyl sulfates obtained by sulfating an alcohol having 8 to 22 carbon atoms, preferably
12 to 16 carbon atoms. The alkyl sulfates have the formula ROSO3-M+ where R is the C8-22 alkyl group and M is a mono- and/or divalent cation.
- Paraffin sulfonates having 8 to 22 carbon atoms, preferably 12 to 16 carbon atoms,
in the alkyl moiety. These surfactants are commercially available as Hostapur SAS
from Hoechst Celanese.
- Olefin sufonates having 8 to 22 carbon atoms, preferably 12 to 16 carbon atoms. U.S.
Pat. No. 3,332,880 contains a description of suitable olefin sulfonates.
- Alkyl glyceryl ether sulfonates having 8 to 22 carbon atoms, preferably 12 to 16 carbon
atoms, in the alkyl moiety.
- Fatty acid ester sulfonates of the formula :
R1 - CH(SO3-M+)CO2R2
wherein R1 is straight or branched alkyl from about C8 to C18, preferably C12 to C16, and R2 is straight or branched alkyl from about C1 to C6, preferably primarily C1, and M+ represents a mono- or divalent cation.
- Secondary alcohol sulfates having 6 to 18, preferably 8 to 16 carbon atoms.
[0019] Other suitable co-surfactants herein are
- Fatty acid amide surfactants having the formula :

wherein R6 is an alkyl group containing from 7 to 21, preferably from 9 to 17, carbon atoms
and each R7 is selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 hydroxyalkyl, and -(C2H4O)xH where x varies from 1 to about 3.
- Polyhydroxy fatty acid amide surfactant of the structural formula :

wherein R1 is H, C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof, preferably
C1-C4 alkyl, more preferably C1 or C2 alkyl, most preferably C1 alkyl (i.e., methyl); and R2 is a C5-C31 hydrocarbyl, preferably straight chain C7-C19 alkyl or alkenyl, more preferably straight chain C9-C17 alkyl or alkenyl, most preferably straight chain C11-C17 alkyl or alkenyl, or mixtures thereof; and Z is a polyhydroxyhydrocarbyl having a
linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain,
or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof. Z preferably
will be derived from a reducing sugar in a reductive amination reaction; more preferably
Z is a glycityl. Suitable reducing sugars include glucose, fructose, maltose, lactose,
galactose, mannose, and xylose. Z preferably will be selected from the group consisting
of -CH2-(CHOH)n-CH2OH, -CH(CH2OH)-(CHOH)n-1-CH2OH, -CH2-(CHOH)2(CHOR')(CHOH)-CH2OH, where n is an integer from 3 to 5, inclusive, and R' is H or a cyclic or aliphatic
monosaccharide, and alkoxylated derivatives thereof. Most preferred are glycityls
wherein n is 4, particularly -CH2-(CHOH)4-CH2OH.
[0020] In formula (I), R
1 can be, for example, N-methyl, N-ethyl, N-propyl, N-isopropyl, N-butyl, N-2-hydroxy
ethyl, or N-2-hydroxy propyl.
[0021] R
2-CO-N< can be, for example, cocamide, stearamide, oleamide, lauramide, myristamide,
capricamide, palmitamide, tallowamide, etc.
[0022] Z can be 1-deoxyglucityl, 2-deoxyfructityl, 1-deoxymaltityl, 1-deoxylactityl, 1-deoxygalactityl,
1-deoxymannityl, 1-deoxymaltotriotityl, etc.
- Betaine detergent surfactants having the general formula :
R - N(+)(R1)2 - R2COO(-)
wherein R is a hydrophobic group selected from the group consisting of 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 about 2 carbon atoms, and similar structures interrupted
by amide or ether linkages; each R1 is an alkyl group containing from 1 to about 3 carbon atoms; and R2 is an alkylene group containing from 1 to about 6 carbon atoms.
- Ethylene oxide condensates, which can be broadly defined as compounds produced by
the condensation of ethylene oxide groups (hydrophilic in nature) with an organic
hydrophobic compound, which can be aliphatic or alkyl aromatic in nature. The length
of the hydrophilic or polyoxyalkylene radical which is condensed with any particular
hydrophobic group can be readily adjusted to yield a water-soluble compound having
the desired balance between hydrophilic and hydrophobic elements.
[0023] Examples of such ethylene oxide condensates suitable as suds stabilizers are the
condensation products of aliphatic alcohols with ethylene oxide. The alkyl chain of
the aliphatic alcohol can either be straight or branched and generally contains from
about 8 to about 18, preferably from about 8 to about 14, carbon atoms for best performance
as suds stabilizers, the ethylene oxide being present in amounts of from about 8 moles
to about 30, preferably from about 8 to about 14 moles of ethylene oxide per mole
of alcohol.
- Cationic quaternary ammonium surfactants of the formula :
[R1(OR2)y][R3(OR2)y]2R4N+X-
or amine surfactants of the formula :
[R1(OR2)y][R3(OR2)y]R4N
wherein R1 is an alkyl or alkyl benzyl group having from about 6 to about 16 carbon atoms in
the alkyl chain; each R2 is selected from the group consisting of -CH2CH2-, -CH2CH(CH3)-, -CH2CH(CH2OH)-, -CH2CH2CH2-, and mixtures thereof; each R3 is selected from the group consisting of C1-C4 alkyl, C1-C4 hydroxyalkyl, benzyl, and hydrogen when y is not 0; R4 is the same as R3 or is an alkyl chain wherein the total number of carbon atoms of R1 plus R4 is from about 8 to about 16, each y is from about 0 to about 10, and the sum of the
y values is from about 0 to about 15; and X is any compatible anion.
[0024] The compositions herein typically comprise from 10% to 60% by weight of the total
composition of a surfactant, or mixtures thereof, preferably from 20% to 55%, most
preferably from 30% to 50%.
Hydrotropes
[0025] As a second essential ingredient, the compositions herein comprise a hydrotrope selected
from the group consisting of salts of cumene sulfonate, toluene sulfonate, xylene
sulfonate, benzene sulfonate or mixtures thereof. Preferred salts are ammonium and
sodium salts.
[0026] The compositions herein typically comprise from 1% to 15% by weight of the total
composition of said hydrotropes, preferably 3% to 10%, most preferably 4% to 6%.
Unsaturated aliphatic terpene alcohol or derivative
[0027] As a third essential ingredient, the compositions herein comprise an unsaturated
aliphatic terpene alcohol or derivates thereof (i.e unsaturated aliphatic terpene
alcohols where the alcohol group is functionalized, e.g. into acetate, formate, propionate,
or the like) or mixtures thereof. Suitable such alcohols or derivatives for use herein
include geraniol, nerol, citronellol, linalool, citronellyl acetate, geranyl acetate,
linalyl acetate, citronellyl formate, geranyl formate, linalyl formate, citronellyl
propionate, geranyl propionate and linalyl propionate.
[0028] Most preferred for use herein is geraniol.
[0029] The compositions herein typically comprise from 0.1% to 3% by weight of the total
composition of said unsaturated aliphatic terpene alcohol, preferably 0.2% to 1%,
most preferably 0.4% to 0.8%.
Optionals
[0030] The compositions herein can comprise a number of other, optional ingredients, as
follows :
[0031] A first optional, but preferred ingredient is a phenolic compound according to the
formula

wherein R, R1, R2, R3, R4 are independently H, a linear or branched, saturated or
unsaturated hydrocarbon chain having from 1 to 20 carbon atoms, preferably from 1
to 10, more preferably from 1 to 4, an alkoxylated hydrocarbon chain according to
the formula Ra(A)
n wherein Ra is a linear or branched, saturated or unsaturated hydrocarbon chain having
from 1 to 20 carbon atoms, preferably from 1 to 10, more preferably from 1 to 4, wherein
A is butoxy, propoxy and/or ethoxy, and n is an integer of 1 to 4, preferably from
1 to 3, or an aryl chain having from 1 to 20 carbon atoms, preferably from 1 to 10
and more preferably from 1 to 4, or mixtures thereof. Highly preferred from that class
of ingredients are Eugenol and Thymol.
[0032] The compositions herein can comprise from 0.1% to 4%, preferably from 0.2% to 1.5%
by weight of the total composition of such a phenolic compound or mixtures thereof.
Magnesium ions :
[0033] The compositions herein preferably comprise from 0% to 2.0%, preferably 0.1% to 1.5%,
most preferably from 0.3% to 1% by weight of the composition, of magnesium ions which
may be added to the liquid detergent compositions of the invention for improved product
stability, as well as improved sudsing and skin mildness.
[0034] It is preferred that the magnesium ions are introduced by neutalization of the acid
form of alkylethoxy surfactants with a magnesium oxide or magnesium hydroxide slurry
in water. Normally, this method is limited by the amount of anionic surfactants in
the composition. An alternative method is to use MgCl2, MgSO4 or other inorganic Mg
salts. These materials are less desirable because they can cause corrosivity problems
(chloride salts), decrease the solubility of the formulations, or cause formulatibility/stability
problems in the compositions. It is desirable for these reasons to limit the addition
of inorganic salts to less than 2%, preferably less than 1% by weight of the anionic
inorganic counterion.
Anti-gelling polymer :
[0035] As another optional component, the compositions of the invention comprise an anti-gelling
polymer which improves the compositions' resistance to gelling. Suitable polymers
for use herein have a molecular weight of at least 500, preferably from 500 to 20000,
more preferably 1000 to 5000, most preferably 1000 to 3000.
[0036] The required amount of anti-gelling polymer can easily be determined by trial and
error, but generally, the compositions herein comprise from 0.5% to 6% by weight of
the total composition of an anti-gelling polymer, or mixtures thereof, preferably
0.5% to 4%, most preferably 1.5% to 3%.
[0037] Suitable polymers for use herein include :
- polyalkylene glycols, preferably polyethylene glycol and polypropylene glycol;
- polyamines; Particularly suitable polyamine polymer for use herein are alkoxylated
or polyalkoxylated polyamines. Such materials can conveniently be represented as molecules
of the empirical structures with repeating units :

wherein R is a hydrocarbyl group, usually of 2-6 carbon atoms; R1 may be a C1-C20 hydrocarbon; the alkoxy groups are ethoxy, propoxy, and the like, and y is 2-30,
most preferably from 10-20; n is an integer of at least 2, preferably from 2-20, most
preferably 3-5; and X- is an anion such as halide or methylsulfate, resulting from the quaternization reaction.
[0038] The most highly preferred polyamines for use herein are the so-called ethoxylated
polyethylene amines, i.e., the polymerized reaction product of ethylene oxide with
ethyleneimine, having the general formula :

when y = 2-30. Particularly preferred for use herein is an ethoxylated polyethylene
amine, in particular ethoxylated tetraethylenepentamine, and quaternized ethoxylated
hexamethylene diamine.
- Terephtalate-based polymers; Suitable terephtalate polymers for use herein include
polymers having the formula :

wherein each R1 is a 1,4-phenylene moiety; the R2 are essentially 1,2-propylene moieties; the R3 are essentially the polyoxyethylene moiety - (CH2H2O)q-CH2-CH2-; each X is ethyl or preferably methyl; each n is from about 12 to about 45; q is
from about 12 to about 90; the average value of u is from about 5 to about 20; the
average value of v is from about 1 to about 10; the average value of u+v is from about
6 to about 30; the ratio u to v is from about 1 to about 6.
[0039] Hihgly preferred polymers for use herein are polymers of the formula :

in which X can be any suitable capping group, with each X being selected from the
group consisting of H, and alkyl or acyl groups containing from 1 to about 4 carbon
atoms, preferably 1 to 2 carbon atoms, most preferably alkyl. Furthermore, the alkyl
group may contain anionic, cationic or nonionic substituents such as sulphonate, sulphato,
ammonium, hydroxy etc. groups. n is selected for water solubility and is a range of
values which generally averages from about 10 to about 50, preferably from about 10
to about 25. There should be very little material, preferably less than about 10 mol
%, more preferably less than 5 mol %, most preferably less than 1 mol %, in which
u is greater than 5. Furthermore there should be at least 20 mol %, preferably at
least 40 mol %, of material in which in ranges from 3 to 5.
[0040] The R
1 moieties are essentially 1,4-phenylene moieties. As used herein, the term "the R
1 moieties are essentially 1,4-phenylene moieties" refers to compounds where the R
1 moieties consist entirely of 1,4-phenylene moieties, or are partially substituted
with other arylene or alkarylene moieties, alkylene moieties, alkenylene moieties,
or mixtures thereof. Arylene and alkarylene moieties which can be partially substituted
for 1,4-phenylene include 1,3-phenylene, 1,2-phenylene, 1,8-naphthylene, 1,4-naphthylene,
2,2-biphenylene, 4,4'-biphenylene and mixtures thereof. Alkylene and alkenylene moieties
which can be partially substituted include ethylene, 1,2-propylene, 1,4-butylene,
1,5-pentylene, 1,6-hexamethylene, 1,7-heptamethylene, 1,8-octamethylene, 1,4-cyclohexylene,
and mixtures thereof.
[0041] Preferably, the R
1 moieties consist entirely of (i.e., comprise 100%) 1,4-phenylene moieties, i.e. each
R
1 moiety is 1,4-phenylene.
[0042] For the R
2 moieties, suitable ethylene or substituted ethylene moieties include ethylene, 1,2-propylene,
1,2-butylene, 1,2-hexylene, 3-methoxy-1,2-propylene and mixtures thereof. Preferably,
the R
2 moieties are essentially ethylene moieties, or, preferably, 1,2-propylene moieties
or mixtures thereof. Preferably, from about 75% to about 100%, more preferably from
about 90% to about 100% of the R
2 moieties are 1,2-propylene moieties.
[0043] The value for n averages at least about 10, but a distribution of n values is present.
The value of each n usually ranges from about 10 to about 50. Preferably, the value
for each n averages in the range of from about 10 to about 25.
[0044] The most preferred polymers for use herein are polymers according to the formula
:

wherein X is methyl, n is 16, R
1 is 1,4-phenylene moiety, R
2 is 1,2-propylene moiety and u is essentially between 3 and 5.
Solvent :
[0045] As another optional component, the compositions of the invention can comprise a solvent
in an effective amount so as to reach the desired viscosity.
[0046] Suitable solvents for use herein include low molecular weight alcohols such as C
1-C
10, preferably C
1-C
4 mono- and dihydric alcohols, preferably ethyl alcohol, isopropyl alcohol, propylene
glycol and hexylene glycol.
[0047] The compositions herein typically comprise from 3% to 20% by weight of the total
composition of an alcohol, or mixtures thereof, preferably 3% to 15%, most preferably
5% to 10%.
[0048] Preferably, the compositions herein are formulated as clear liquid compositions.
By "clear" it is meant isotropic, stable and transparent. In order to achieve isotropic
compositions, the use of solvents and hydrotropes is well known to those familiar
with the art of dishwashing formulations. Those clear compositions are preferably
packaged in transparent containers, which can typically be made out of plastic or
glass.
[0049] In addition to the optional ingredients described hereinbefore, the compositions
can contain other optional components suitable for use in liquid dishwashing compositions
such as perfume, dye, opacifiers, enzymes, builders and chelants and pH buffering
means so that the compositions herein generally have a pH of from 5 to 11, preferably
6.0 to 10.0, most preferably 7 to 9 measured at a 10% solution in water.
Method :
[0050] In the method aspect of this invention, soiled dishes are contacted with an effective
amount, typically from about 0.5 ml. to about 20 ml. (per 25 dishes being treated),
preferably from about 3 ml. to about 10 ml., of the detergent composition of the present
invention. The actual amount of liquid detergent composition used will be based on
the judgement of user, and will typically depend upon factors such as the particular
product formulation of the composition, including the concentration of active ingredients
in the compositon, the number of soiled dishes to be cleaned, the degree of soiling
on the dishes, and the like.
[0051] The particular product formulation, in turn, will depend upon a number of factors,
such as the intended market (i.e., U.S., Europe, Japan, etc.) for the composition
product.
[0052] In the method herein, the soiled dishes are preferably immersed into a water bath
with or without a liquid dishwashing detergent as described herein. A dish implement,
i.e. a device suitable for absorbing a liquid dishwashing detergent such as a sponge
or a dishcloth, is placed directly onto or contacted with a separate quantity of undiluted
liquid dishwashing composition as described herein for a period of time typically
ranging from about 3 to about 10 seconds. The absorbing device, and consequently the
undiluted liquid dishwashing composition, is then contacted individually to the surface
of each of the soiled dishes to remove said soiling. The absorbing device is typically
contacted with each dish surface for a period of time ranging from about 5 to about
30 seconds, although the actual time of application will be dependent upon factors
such as the degree of soiling of the dish. The contacting of the absorbing device
to the dish surface is preferably accompanied by concurrent scrubbing.
[0053] After all the dishes to be cleaned have been cleaned, the dish implement is preferably
contacted, e.g. soaked with neat product and left to dry. There is little or no bacterial
growth in the dish implements used according to the method herein even over extended
usage, and contaminated dish implements (i.e. dish implements contaminated by previous
uses with other compositions) also recover after one or several uses in a method according
to the present invention.
Examples
[0054] The following compositions, which illustrate the invention, are made by mixing together
the listed ingredients in the listed proportions.
| Example 1 |
|
Example 2 |
|
| Alcoholethoxylate (2.2) sulfate |
22 |
Alcoholethoxylate (2.2) sulfate |
22 |
| Amine oxide |
3 |
Amine oxide |
3 |
| Nonionic |
7 |
Nonionic |
7 |
| Glucose amide |
5 |
Glucose amide |
5 |
| Betaine |
2 |
Betaine |
2 |
| Mg++ |
0.5 |
Mg++ |
0.5 |
| Ethanol |
7 |
Ethanol |
7 |
| Sodium cumene sulfonate |
5 |
Sodium toluene sulfonate |
5 |
| Polypropylene glycol (2000) |
2.00 |
Polypropylene glycol (2000) |
2.00 |
| Propylene glycol |
1.00 |
Propylene glycol |
1.00 |
| Geraniol |
0.60 |
Geraniol |
0.25 |
| Water |
balance |
Thymol |
0.25 |
| |
|
Eugenol |
0.25 |
| |
|
Water |
balance |
| |
|
|
|
| pH |
7.8 |
pH |
7.8 |
| Example 3 |
|
Example 4 |
|
| Alcoholethoxylate (3.0) sulfate |
19 |
Alcoholethoxylate (3.0) sulfate |
11 |
| Alcyl polyglycoside |
2 |
Nonionic |
6 |
| Nonionic |
13 |
Amide |
2 DEA |
| Amide |
2 DEA |
Amine oxide |
7 |
| Amine oxide |
6 |
Mg++ |
0.04 |
| Mg++ |
0.02 |
Sodium toluene sulfonate |
8.00 |
| Ethanol |
3 |
Geraniol |
0.30 |
| Sodium toluene sulfonate |
5 |
Thymol |
0.30 |
| Nacitrate |
3 |
Eugenol |
0.30 |
| Geraniol |
0.60 |
Water |
balance |
| Water |
balance |
|
|
| |
|
|
|
| pH |
6.4 |
pH |
6.8 |
| Example 5 |
|
Example 6 |
|
| Alcoholethoxylate (0.6) sulfate |
26 |
Alcoholethoxylate (0.6) sulfate |
26 |
| Amine oxide |
2 |
Amine oxide |
2 |
| Betaine |
2 |
Betaine |
2 |
| Glucose amide |
1.5 |
Glucose amide |
1.5 |
| Nonionic |
5 |
Nonionic |
5 |
| Mg++ |
0.50 |
Mg++ |
0.50 |
| Ethanol |
7 |
Ethanol |
7 |
| Sodium cumene sulfonate |
3 |
Sodium xylene sulfonate |
5 |
| Geraniol |
0.60 |
Geraniol |
0.20 |
| Water |
balance |
Thymol |
0.20 |
| |
|
Eugenol |
0.20 |
| |
|
Water |
balance |
| |
|
|
|
| pH |
7.8 |
pH |
7.8 |
| Example 7 |
|
Example 8 |
|
| Alcoholethoxylate (2.2) sulfate |
27 |
Sodium parafinesulfate |
7 |
| Amine oxide |
6 |
Alcoholethoxylate (2.0) sulfate |
22 |
| Nonionic |
4 |
Nonionic |
0.50 |
| GS-base |
6 |
Amide |
0.3 DEA |
| Ethanol |
6 |
Betaine |
0.50 |
| Calcium xylene sulfonate |
4 |
Ethanol |
0.60 |
| Geraniol |
0.60 |
Sodium toluene sulfonate |
5 |
| Triclosan |
0.25 |
Water |
balance |
| Water |
balance |
|
|
| |
|
|
|
| pH |
7.80 |
pH |
6.30 |
1. An aqueous liquid dishwashing composition comprising
- a surfactant,
- a hydrotropic selected from the group consisting of salts of cumene sulfonate, toluene
sulfonate, xylene sulfonate, benzene sulfonate or mixtures thereof; and
- an unsaturated aliphatic terpene alcohol or derivative.
2. A composition according to claim 1 which comprises from 10% to 60% by weight of the
total composition of said surfactant, from 1% to 15% by weight of the total composition
of said hydrotrope, and from 0.1% to 3% by weight of the total composition of said
unsaturated aliphatic terpene alcohol or derivative.
3. A composition according to claim 2 which comprises from 20% to 55% by weight of the
total composition of said surfactant, from 3% to 10% by weight of the total composition
of said hydrotrope, and from 0.2% to 1% by weight of the total composition of said
unsaturated aliphatic terpene alcohol.
4. A composition according to the preceding claims wherein said salts of cumene sulfonate,
toluene sulfonate, xylene sulfonate and benzene sulfonate is the sodium salt.
5. A composition according to the preceding claims wherein said unsaturated aliphatic
terpene alcohol is geraniol.
6. A composition according to the preceding claims which additionally comprises a phenolic
compound of the formula

wherein R, R1, R2, R3, R4 are independently H, a linear or branched, saturated or
unsaturated hydrocarbon chain having from 1 to 20 carbon atoms, preferably from 1
to 10, more preferably from 1 to 4, an alkoxylated hydrocarbon chain according to
the formula Ra(A)
n wherein Ra is a linear or branched, saturated or unsaturated hydrocarbon chain having
from 1 to 20 carbon atoms, preferably from 1 to 10, more preferably from 1 to 4, wherein
A is butoxy, propoxy and/or ethoxy, and n is an integer of 1 to 4, preferably from
1 to 3, or an aryl chain having from 1 to 20 carbon atoms, preferably from 1 to 10
and more preferably from 1 to 4, or mixtures thereof.
7. A composition according to claim 6, wherein said phenolic compound is eugenol or thymol,
or mixtures thereof.
8. A composition according to claims 6 and 7 which comprises from 0.1 % to 4% by weight
of the total composition of said phenolic compound, or mixtures thereof.
9. A method of washing dishes, wherein an effective amount of the composition according
to claims 1-8 is applied onto a dish implement, and said dish implement is then contacted
with dishes to be cleaned.