Field of the Invention
[0001] The invention relates to the use of a composition comprising cationic fabric softeners,
preferably quaternary ammonium esters and (C₃-C₁₀) alkyl/aryl polyammonium salts.
[0002] These polyammonium salts are used to replace partially or fully calcium chloride
to aid the cationic fabric softeners in depositing on fabrics while reducing the inter-cationic
interferences usually leading to low deposition densities.
Background of the Invention
[0003] Compositions containing polyammonium salts and conventional fabric softeners are
disclosed in US application 07/88/979. However, no mention of the use of these polyammonium
salts as deposition density aid is disclosed in this document. FR-A-1581392 discloses
diamine salts falling within the definition of the polyammonium salts of the present
invention. However, these diamine salts are disclosed in the context of washing powders
including anionic detergents.
[0004] GB-A-2006237 discloses polymers comprising a monomere of alky-diamines. These monomeres
also fall within the definition of the polyammonium salts of the present invention.
The compositions disclosed are used in hair care formulations and the polymers derived
from the polyammonium monomeres are said to have improved compatibility with anionic
surfactants.
[0005] EP-A-69948 and JP-A-90012203 disclose polyammonium compounds in the context of fabric
treatment compositions. However, no indication of these compounds falling within the
definition of the present invention has been found. The problem underlying the present
invention is to provide viscosity control and stability of fabric softening compositions,
to increase the density of cations which can be deposited on a fabric fiber and, at
the same time, to perform anionic scavenging for carry-over detergent from the main
wash. These problems had all been solved individually before, however, their combination
with the additional condition that no adverse effects in other characteristics of
a fabric softener composition would be acceptable is the main objective of the present
invention.
Summary of the Invention
[0006] It now has been found surprisingly that the use of soluble carbohydrate polyammonium
salts replacing calcium chloride does satisfy the complex objective of the present
invention. Therefore, the present invention relates to the use of soluble polyammonium
salts for viscosity control, deposition density aid and anionic scavenging in rinse
added fabric softening compositions.
[0007] The fabric softening compositions comprise insoluble fabric softening agent and,
at least 0.1 % by weight of a (C₃-C₁₀)alkyl or aryl polyammonium salt. Preferred embodiments
according to the present invention are indicated in the dependent claims attached
to this specification.
[0008] In an alternative aspect to the polyammonium salts partially quaternized or non-quaternized
polyammonia can be used provided the rinse added composition is used in an environment
such that the non-quaternized or partially non-quaternized ammonia becomes protonated
through acidic buffering of the rinse liquid. Any useful acids buffering the rinse
liquid can be used in this context and the ammonia can be seen as the precursor of
quaternized ammoniums.
Detailed description of the Invention
[0009] In the following the essential compounds and optional compounds of the composition
as used in the invention will be described separately. Percentages, when they are
indicated, are by weight of the final composition. For optional compounds, reference
is made here to the general knowledge of those skilled in the art and the prior art
documents mentioned herein.
The cationic fabric softening compound.
[0010] The essential fabric softening compound of the present invention is typically a non-soluble
quaternized ammonium, preferably a di-ester quaternary ammonium. Preferably the cationic
fabric softening compound is present in a total amount of at least 15 %, more preferably
in an amount of 15 % to 25 %, not accounting for optional cationic fabric softeners.
[0011] According to the present invention the preferred ester ammonium can have the general
formula :
(R)
4-m - N⁺ - [(CH₂)n - Y - R²]m X⁻
wherein
each Y = -O-(O)C-, or -C(O)-O-;
m = 1, 2 or 3, preferably 2;
each n = 1 to 4
each R substituent is a short chain C₁-C₆, preferably C₁-C₃ alkyl or hydroxyalkyl
group, e.g.,methyl (most preferred), ethyl, propyl, hydroxyethyl, and the like, benzyl
or mixtures thereof; each R² is a long chain C₁₂-C₂₂ hydrocarbyl, or substituted hydrocarbyl
substituent, preferably C₁₅-C₁₉ alkyl and/or alkylene, most preferably C₁₅-C₁₇ straight
chain alkyl and/or alkylene; and the counterion, X⁻, can be any softener-compatible
anion, for example, chloride, bromide, methylsulfate, formate, sulfate, nitrate, and
the like.
[0012] It will be understood that substituents R and R² can optionally be substituted with
various groups such as alkoxyl or hydroxyl groups, and/or can be saturated, unsaturated,
straight and/or branched so long as the R² groups maintain their basically lipophilic
character. The preferred compounds can be considered to be di-ester variations of
ditallow dimethyl ammonium chloride(DTDMAC), which is a widely used fabric softener.
At least 80% is in the di-ester form, and from 0 % to about 20% can be monoester.
[0013] As used herein when the di-ester is specified, it will include the monoester that
is normally present, but not additional monoester that is added. For softening, the
percentage of di-ester should be as high as possible, preferably more than 90%.
[0014] The above compounds used as the primary active softener ingredient in the practice
of this invention can be prepared using standard reaction chemistry. In one synthesis
of a di-ester variation of DTDMAC, an amine of the formula RN(CH₂CH₂OH)₂ is esterified
at both hydroxyl groups with an acid chloride of the formula R²C(O)C1, then quaternized
with an alkyl halide, RX,, to yield the desired reaction product (wherein R and R²
are as defined herinbefore). The following are non-limiting examples (wherein all
long-chain alkyl substituents are straight-chain):
[HO-CH(CH₃)CH₂][CH₃]N⁺[CH₂CH₂OC(O)C₁₅H₃₁]₂ Br⁻
[C₂H₅]₂N⁺[CH₂CH₂OC(O)C₁₇H₃₅]₂ Cl⁻
[CH₃][C₂H₅]N⁺[CH₂CH₂OC(O)C₁₃H₂₇]₂ I⁻
[C₃H₇][C₂H₅]N⁺[CH₂CH₂OC(O)C₁₅H₃₁]₂ (SO₄-CH₃)⁻
[CH₃]₂N⁺-CH₂CH₂OC(O)C₁₅H₃₁ Cl⁻
CH₂CH₂OC(O)C₁₇H₃₅
[CH₂CH₂OH][CH₃]N⁺[CH₂CH₂OC(O)R²]₂ Cl⁻
[CH₃]₂N⁺[CH₂CH₂OC(O)R²] Cl⁻
where -C(O)R2 is derived from soft or hard tallow, or mixtures thereof.
[0015] Since the foregoing compounds (di-esters) are somewhat labile to hydrolysis (hence
their beneficial degradability), they should be handled rather carefully when used
to formulate the compositions herein. For example, stable liquid compositions herein
are formulated at a pH in the range of about 2 to about 5, preferably from about 2
to about 4.5, more preferably from about 2 to about 4. The pH can be adjusted by the
addition of a Bronsted acid. pH ranges for making stable softener compositions containing
di-ester quaternary ammonium fabric softening compounds are disclosed in U.S. 4,767,547.
[0016] Examples of suitable Bronsted acids include the inorganic mineral acids, carboxylic
acids, in particular the low molecular weight (C₁-C₅) carboxylic acids, and alkylsulfonic
acids. Suitable inorganic acids include HCl, H₂SO₄, HNO₃ and H₃PO₄. Suitable organic
acids include formic, acetic, methylsulfonic and ethylsulfonic acid. Preferred acids
are hydrochloric and phosphoric acids. The presence of the aromatic acids which are
useful in the present invention also helps to stabilize the di-ester compounds.
[0017] The preferred di-ester quaternary ammonium fabric softening compound (DEQA) can also
have the general formula :

wherein each R, R² and X have the same meanings as before. Such compounds include
those having the formula :
[CH₃]₃ N⁺[CH₂CH(CH₂OC(O)R²)OC(O)R²] Cl⁻
where -OC(O)R2 is derived from soft or hard tallow, or mixtures thereof.
[0018] Preferably each R is a methyl or ethyl group and preferably each R² is in the range
of C₁₅ to C₁₉. Degrees of branching, substitution and/or non-saturation can be present
in the alkyl chains. The anion X⁻ in the molecule is preferably the anion of a strong
acid and can be, for example, chloride, bromide, iodide, sulfate and methyl sulfate;
the anion can carry a double charge in which case X⁻ represents half a group. These
compounds, in general, are more difficult to formulate as stable liquid compositions.
These types of compounds and general methods of making them are disclosed in U.S.
4,137,180.
[0019] For stability of the composition and to enhance concentratability, as well as the
derived isotopic characteristic, it is beneficial to have a high level of unsaturation
in the lipophilic long chain hydrocarbons. An iodine value of above 30 up to 100,
preferably above 50, has been found to be beneficial. Also beneficial, particularly
if the iodine value is not above 70, are double bonds of the cis configuration due
to their melting point difference vs trans double bonds.
[0020] Other cationic materials with ring structures such as alkyl imidazoline, imidazolinium,
pyridine, and pyridinium salts having a single C₁₂-C₃₀ alkyl chain can also be used.
Very low pH is required to stabilize, e.g. imidazoline ring structures. Some alkyl
imidazolinium salts useful in the present invention have the general formula :

wherein Y² is -C(O)-O-, -O-(O)-C-, -C(O)-N(R⁵), or -N(R⁵)-C(O)-
in which R⁵ is hydrogen or a C₁-C₄ alkyl radical; R⁶ is a C₁-C₄ alkyl radical; R⁷
and R⁸ are each independently selected from R and R² as defined hereinbefore for the
single-chain cationic surfactant with only one being R².
[0021] Some alkyl pyridinium salts useful in the present invention have the general formula
:
R² - N⁺ X⁻
wherein R² and X⁻ are as defined above. A typical material of this type is cetyl pyridinium
chloride.
Further optional cationic and other softening compounds have been described or referred
to in PCT application US-93-04107 filed May 3, 1993.
[0022] The fabric softener compositions optionally further contain quaternary - di or poly
- ammoniums as described in detail in EP-A-503155 and EP-A-507003. These ammoniums
are non-soluble cationic fabric softeners.
Polyammonium Salt
[0023] (C₃-C₁₀) alkyl or aryl polyammonium salts, or the ammonia precursors in a protonating
environment are used according to the present invention for viscosity control, as
deposition density aid and for anionic scavenging in rinse added fabric softening
compositions. They are present in the fabric softening compositions in amounts of
at least 0.1 %, preferably from 0.1 % to 5 %, most preferably from 0.2 % to 1 % by
weight of the composition.
[0024] Hereinafter the polyammonium salts will be described with the nitrogen in its ammonium
state but, as indicated above, they can be used with one or all nitrogens in their
ammonia state, provided that they become protenated upon use. This in ensured by having
sufficient protons available e.g. by the presence of an acid as described above.
[0025] Preferred polyammonium salts are (C₃-C₈) alkyl polyammonium salts, particularly di-ammonium
salt. Examples of such salts are
- 1,5-di-ammonium-2-methyl-panthene di-chloride.
- 1-ammonium-chloride-5-ammonia-hexoic acid (lysine-monohydrochloride).
[0026] While not wishing to be bound by theory, it has been considered by the inventors
that these compounds have a substantially better viscosity control, deposition density
aid and anionic scavenging because they distance the positive charges, while keeping
them connected within one molecule.
[0027] This "partial individualisation of charges" can be compared for di-ammoniums with
a model of two positive charges connected by a string which provides a high level
of independence between the charges in comparison to a double charged calcium. On
the other hand the density of the two charges connected by the string is higher than
two independently charged molecules, since the string length is small relative to
the distance which would be reached by electrical repellance for an even distribution
of independently charged molecules on an identical number of charges.
[0028] Using the polyammonium salts provides a better control of the viscosity of the composition
in that the polyammonium salts allow lower and higher temperatures without unacceptable
viscosity conditions (i.e. gelling at low temperatures, watery appearance at high
temperatures) relative to a comparably formulated composition using CaCl₂.
[0029] Further the use of the polyammonium salts allows better scavenging of carry over
anionic surfactants (which is possibly due to the "partial
individualisation of charges") and hence prevents depletion of the active cationic softening compound.
[0030] Further the limited string length between the "
partially individualized charges" helps to bridge electrical repellent surface forces between
deposited fabric softener actives and thereby aids in the deposition density of rinse
added fabric softeners.
Optional ingredients
[0031] As an optional viscosity modifier single long chain cationic surfactants, which are
water soluble, can be present in amounts of 0% up to 15%. Such single long-chain-alkyl
surfactants useful in the present invention are, preferably quaternary ammonium salts
of the general formula:
[R²N⁺R₃] X⁻
wherein the R² group is C₁₀-C₂₂ hydrocarbon group, preferably C₁₂-C₁₈ alkyl group
or the corresponding ester linkage interrupted group with a short alkylene (C₁-C₄)
group between the ester linkage and the N, and having a similar hydrocarbon group,
e.g. a fatty acid ester of choline, preferably C₁₂-C₁₄ (coco) choline ester and/or
C₁₆-C₁₈ tallow choline ester. Each R is a C₁-C₄ alkyl or substituted (e.g. hydroxy)
alkyl, or hydrogen, preferably methyl, and the counterion X⁻ is a softener compatible
anion, for example, chloride, bromide, methyl sulfate, etc.
[0032] The ranges above represent the amount of the water soluble single-long-chain-alkyl
cationic surfactant which is added to the composition of the present invention. The
ranges do not include the amount of monoester which is already present in the essential
fabric softening compound.
[0033] The long chain group R², of the single-long-chain-alkyl cationic surfactant, typically
contains an alkylene group having from about 10 to about 22 carbon atoms, preferably
from about 12 to about 18 carbon atoms. This R² group can be attached to the cationic
nitrogen atom through a group containing one, or more, ester, amide, ether, amine,
etc., preferably ester, linking groups which can be desirable for increased hydrophilicity,
biodegradability, etc. Such linking groups are preferably within about three carbon
atoms of the nitrogen atom. Suitable biodegradable single-long-chain alkyl cationic
surfactants containing an ester linkage between the nitrogen and the long chain are
described in U.S. 4,840,738.
[0034] It will be understood that the main function of the water-soluble cationic surfactant
is to lower the viscosity and/or increase the dispersibility of the essential fabric
softener compound and it is not therefore, essential that the cationic surfactant
itself have substantial softening properties, although this may be the case. Also,
surfactants having only a single long alkyl chain, presumably because they have greater
solubility in water, can protect the essential fabric softener compound from interacting
with anionic surfactants and/or detergent builders that are carried over into the
rinse.
[0035] Another optional compound improving the viscosity of highly concentrated fabric softening
compositions are non-ionic surfactants. Suitable non-ionic surfactants to serve as
viscosity/dispersibility modifier include addition products of ethylene oxide and,
optionally, propylene oxide, with fatty alcohols, fatty acids, fatty amines, etc.
[0036] Any of the alkoxylated materials of the particular type described hereinafter can
be used as the non-ionic surfactant. The non-ionics are used at a level of from 0%
to about 15%. Suitable compounds are substantially water-soluble surfactants of the
general formula :
R⁹ - Y - (C₂H₄O)
Z - C₂H₄OH
wherein R⁹ is selected from the group consisting of primary, secondary and branched
chain alkyl and/or acyl hydrocarbyl groups; primary, secondary and branched chain
alkenyl hydrocarbyl groups; and primary, secondary and branched chain alkyl- and alkenyl-substituted
phenolic hydrocarbyl groups; said hydrocarbyl groups having a hydrocarbyl chain length
of from 8 to about 20, preferably from about 10 to about 18 carbon atoms. More preferably
the hydrocarbyl chain length is from 16 to 18 carbon atoms. In the general formula
for the ethoxylated non-ionic surfactants herein, Y is typically -O-, -C(O)O-, -C(O)N(R)-,
or -C(O)N(R⁹)R-, in which R⁹, and R, when present, have the meanings given hereinbefore,
and/or R can be hydrogen, and z is at least about 8, preferably at least about 10-11.
Performance and, usually, stability of the softener composition decrease when fewer
ethoxylate groups are present.
[0037] Examples of non-ionic surfactants are disclosed in further detail in PCT application
US-93-04107 filed May 3, 1993. All of the typical fabric softener compounds usual
in the art may further be present in the compositions according to the present invention,
in particular enzymes (protease, lipase, cellulase and amylase, especially cellulase),
perfumes, dyes, solvents, polymers, bacterial and fungal stabilizers and other compounds.