Background of the invention
1. Field of the invention
[0001] This invention deals with liquid detergent products.
2. Description in the art practices
[0002] In recent years, it has become common for detergent manufacturers to move away from
powdered or granular detergent products to liquids. The liquid detergents usually
contain a substantial amount of water in the product. Liquid detergent products are
considerably easier to manufacture than are granular detergent products. The latter
materials require a substantial amount of capital investment for spray-drying towers.
Additionally, a consumer preference has emerged for the liquid products due to their
more concentrated form. Most liquid detergent products do not contain the inert inorganic
material which is required to give spray-dried granules their crisp, non-caking structure.
Accordingly, the liquid detergent products are used in much smaller amounts while
giving approximately the same level of active ingredients in the wash water.
[0003] A second consumer preference is for a product having a desirable viscosity. Products
which are water- thin are not desirable. In part, products which are too thin are
more likely to be spilled by the consumer when attemping to handle the approximately
four-liter bottles in which liquid detergents are commonly packaged. Another advantage
of liquid detergent products is that they can be applied directly to a heavily soiled
portion of a garment. In such cases, raising the viscosity of a normally thin liquid
detergent product allows the detergent to stay on the soiled area longer. A market
also exists for shampoo, liquid hand soaps, body soaps, dishwashing liquids, cosmetics
and personal care products having a relatively high viscosity.
[0004] Various methods of thickening liquid detergent products are known in the art. These
methods employ cellulosic polymer such as carboxymethylcellulose, guar gums, xanthan,
colloidal silicates or clays. The glucoside ester-ether adducts as described in United
States Patent 4,450,090 to Kinney issued May 22,1984 are suggested as thickeners for
olefin sulfonates.
[0005] The use of short chain alkyl polyglycosides to reduce viscosity in aqueous liquid
detergent compositions is taught in European Patent Application No. 0 136 844, published
10.04,85. The particular glycosides taught in this application are those materials
containing from 2 to 6 carbon atoms in the alkyl portion and from 1 to 10 saccharide
units. United States Patent 3,219,656 issued November 23, 1965 to Boettner teaches
the production of alkyl polyglycosides including those glycosides prepared from an
oxo- undecyl alcohol, and as compounds, the 2,6,8-trimethyl-4-nonanol glycosides.
[0006] Renauto in United States Patent 3,721,633 issued March 20, 1973 teaches aqueous built
liquid detergent compositions disclosing alkyl polyglycosides and anionic surfactants
in combination with inorganic detergent builders. United States Patent 4,077,894 issued
March 7, 1978 to Langdon et al describes glycol-based anti-freeze products containing
a glycoside for the purpose of foam suppression.
[0007] Payne et al in United States Patent 4,396,520 issued August 2,1983 describes the
combination of alkyl polyglycosides and calcium-sensitive anionic surfactants in granular
detergent compositions. United States Patent 4,446,042 issued May 1, 1984 to Leslie
describes the preparation of detergent products containing nonionic surfactants, cationic
surfactants, anionic brighteners and glycosides in heavy-duty liquid detergent compositions.
[0008] Rau in United States Patent 4,465,828 issued August 14, 1984 describes alkyl saccharides
(glycosides) which are stated to have improved color due to the inclusion of a hydroxypolycarboxylic
acid. Rau also discloses that the glycosides may be formed from a saccharide and a
fatty alcohol containing from 1 to 20 carbon atoms which may be primary or secondary
or having a straight or branched chain.
[0009] European Patent Application No. 0070075 laid open on January 19, 1983 to Cook etal
describes alkyl polyglycoside detergent compositions which contain as an anionic cosurfactant
an alkyl benzene sulfonate, an alkyl glycerol ether sulfonate, an alpha-olefin sulfonate,
an alkyl polyethoxy carboxylate or mixtures of the foregoing. Arnaudis in Europen
Patent Application No. 0077167 published on April 20,1983 describes a process of manufacturing
surface-active glycosides in the presence of reducing acids. The Arnaudis application
states that the glycosides may contain branching in the hydrophobic portion and that
the alcohol may be primary or secondary.
[0010] Mao in European Patent Application No. 0092875 published on November 2,1983 discloses
a process for the production of alkyl glycosides involving a wiped-film evaparator.
Mao further teaches that the fatty portion of the glycoside may be a primary or secondary
alcohol having straight or branched chains which may be either saturated or unsaturated
and may contain either linkages as well. Substantially similar teachings to European
Patent Application No. 0092875 are also found in United States Patent 4,393,203 issued
July 12, 1983 to the same inventor.
[0011] European Patent Application No. 0096917 (laid open December 12, 1983), to Farris
describes the production of glycosides containing from 8 to 25 carbon atoms in the
alcohol residue of the glycoside. The alcohol residue may be primary or secondary,
straight or branched and obtained from a saturated or unsaturated material. Europan
Patent Application No. 0105556 to Jones et al made public April 18, 1984 describes
detergent products containing glycosides, nonionics, and anionics. Canadian Patent
919,424 to Culver et al issued January 23, 1973 describes alkaline drain cleaning
compositions containing phosphate esters, and a glycoside or an anionic surfactant.
[0012] To the extent that the references mentioned herein are applicable to the present
invention, they are incorporated by reference. Throughout the specification and claims,
percentages and ratios are by weight, temperatures in degrees Celsius, and pressures
in atmospheres over ambient unless otherwise indicated.
Summary of the invention
[0013] This invention describes a liquid detergent comprising:
(a) from 3% to 45% by weight of an anionic surfactant:
(b) from 0.3% to 20% by weight of monoglycoside represented as ROG wherein R is the
hydrophobic moiety (fatty organic portion) of the molecule containing from 10 to 24
carbon atoms O is an oxygen, preferably in the 1 position of the saccharide, and G
represents the saccharide and
(c) from 30% to 95% by weight of water,
and wherein the content, if any, of glycoside compounds having a degree of polymerization
(D.P.) of 2 or more within said composition is such that the average D.P. of all glycoside
compounds within said composition is less than 1.4.
[0014] Also described is a method of increasing the viscosity of an aqueous liquid detergent
composition containing an anionic surfactant by including therein from 0.3% to 20%
by weight of an alkyl monoglycoside represented as ROG wherein R is the hydrophobic
moiety (fatty organic portion) of the molecule containing from 10 to 24 carbon atoms,
O is an oxygen, preferably in the 1 position of the saccharide, and G represents the
saccharide, to thicken the aqueous liquid detergent composition and by ensuring that
the content, if any, of glycoside compounds having a degree of polymerization (D.P.)
of 2 or more within said composition is such that the average D.P. of all glycoside
compounds within said composition is less than 1.4.
Detailed description of the invention
[0015] The glycosides. which have been found useful in increasing the viscosity of aqueous
detergent products containing an anionic surfactant are monoglycosides.
[0016] The term monoglycoside as used herein includes such substituted monosaccharides as
fructosides, glucosides, mannosides, galactosides, talosides, allosides, altrosides,
idosides, arabinosides, xylosides, lyxosides, ribosides, and mixtures thereof.
[0017] The monoglycosides useful in raising the viscosity of the detergent composition are
represented as

wherein R is the hydrophobic moiety (fatty organic portion) of the molecule containing
from 10 to 24 carbon atoms, 0 is an oxygen, preferably in the 1 position of the saccharide,
and G represents the saccharide. While more than one R group may be on each saccharide
molecule (attached as an ether linkage), the difficulty and expense outweigh the benefit
of introducing more than the initial hydrophobic moiety.
[0018] It is observed that the benefits of the invention in the order of importance are
that the glycoside first be a monoglycoside, and second that the glycoside contain
from 10 to 24, and preferably from 12 to 18 carbon atoms in the hydrophobic moiety
of the molecule. Preferably a third condition is that the hydrophobic moiety on the
monoglycoside be branched either by using a secondary alcohol or by branching within
the hydrophobic moiety. A further variable herein is that the branching is desirably
multiple branched, e.g. several groups. The oxo alcohols having multiple methyl branching
are particularly desirable.
[0019] The following is a brief description of the manner of obtaining the monoglycoside
utilized herein. The monoglycoside is preferably a glucoside and may be obtained as
is described in United States Patent 3,219,656 to Boettner issued November 23, 1965
or the article entitled "Preparation and Properties of Pure Alkyl Glucosides, Maltosides,
and Maltotriosides by Koeltzow and Urfer, JAOCS, V. 61, No. 10, p. 1651 (1984). The
amount of monoglycoside obtained can be maximized by utilizing an excess of alcohol
to promote the acetal formation over the polymerization reaction.
[0020] Particular alcohols which may be utilized herein are n-dodecyl, n-tridecyl, n-tetradecyl,
n-pentadecyl, n-hexadecyl, n-octadecyl, n-decyl, tetramethyl 1-nonanol, and trimethyl-nonanol.
Secondary alcohols which may be used to obtain the monoglycoside include 2-decanol,
2-undecanol, 2-dodecanol and 2-tridecanol.
[0021] Additional alcohols which may be employed in forming the monoglycoside include guerbet
alcohols such as are described in United States Patent 4,425,458 to Lindner issued
January 10, 1984.
[0022] The anionic surfactants which are useful herein are alkyl ether sulfates, alkyl benzene
sulfonates, alkyl sulfates, olefin sulfonates, paraffin sulfonates and soap (carboxylate).
Particularly valuable are those anionic surfactants containing from 10 to 20 carbon
atoms in the hydrophobic portion of the molecule. A preferred surfactant group is
the alpha-olefin sulfonates. A second preferred surfactant is an alkyl ether sulfate
which contains an average of from 1 to 3 ethoxy groups in the molecule. The preferred
cation for the anionic surfactants is sodium or potassium or mixtures thereof. Further
anionic surfactants which may be employed are those described in United States Patent
4,476,045 to O'Lenick issued October 9, 1984.
[0023] Alkoxylated nonionic surfactants are to be minimized as an ingredient in the compositions
of this invention. It has been found that nonionics such as ethoxylated alcohols reduce
the viscosity thereby negating the advantages of the monoglycosides described herein.
Typically the alkoxylated nonionic should not be present at greater than 10%, preferably
less than 5% by weight. It has also been observed that higher glycosides (DP
2 and greater) reduce the viscosity as the DP increases and the hydrophobic moiety
decreases. Therefore higher (DP
2 and greater) glycosides are minimized such that the average DP is less than 1.4,
preferably less than 1.3.
[0024] The amount of glycoside as monoglycoside in the product is preferably from 0.5% to
10%, most preferably from 1 % to 5% by weight. The amount of anionic surfactant in
the formula is preferably from 5% to 30%, most preferably from 8% to 25% by weight.
The level of water in the product is conveniently set at from 35% to 92%, preferably
from 40% to 90% by weight. It is also desirable that the amount of monoglycoside as
used herein be in a weight ratio to the anionic surfactant of from 4:1 to 1:60, preferably
from 2:1 to 1:10.
[0025] The ingredients of the present invention may be combined in any convenient manner.
A preferred order of addition of the components involves obtaining the monoglycoside
in its solid state, and adding thereto a mixture of the anionic surfactant and water.
As the anionic surfactant is usually a fairly concentrated material, it is often necessary
to add further water to the end mixture to obtain the desired product. As the viscosity
will increase substantially as the monoglycoside is added, adequate mixing and pumping
capabilities should be utilized to ensure that the product may be efficiently transferred.
[0026] Desirably the product herein will have a viscosity of from 50 to 100,000 preferably
from 150 to 10,000 mPa - s at 25°C as determined by a Brookfield cone-plate viscometer
having a cone angle of 1.57°.
[0027] The compositions of the present invention may also include all manner of materials
normally found in aqueous liquid detergent products including, compatible hydrotropes,
optical brighteners and dyes, perfumes, enzymes and the like. Additional ingredients
which may be included in the composition of the present invention include builders
such as tripolyphosphate, nitrilotriacetate, pyrophosphate and any of the organic
builders as discussed in European Patent Application No. 0150930 published 07.08.85.
[0028] The products of the invention when utilized as laundry detergent products are normally
employed at from 0.05% to 1% by weight of the active ingredients in the wash water.
It is recommended that the laundry be washed at from 37°C to 60°C.
[0029] The products herein may also be formulated as liquid dishwashing or hard surface
cleaning products in a similar fashion. As dishwashing products are typically of a
lower viscosity than is desired for a laundry detergent product, smaller quantities
of the monoglycoside may be used. The products described herein are also useful in
cosmetics, handcleaners, body soaps, shower gels, shaving creams or gels and hair
shampoos. The pH of the products described in the Summary should be from 5 to 8 when
diluted on a dry solids basis at 0.1% by weight when no other pH influencing ingredients
are present. The products are conveniently adjusted to a pH of from 2.5 to 7.8, preferably
3 to 7.5, most preferably 3 to 7.2 to give maximum thickening. Any convenient buffer
or pH adjusting material such as citric acid and its salts may be employed therein.
[0030] The following are suggested exemplifications of the present invention.
Example I
[0031] Several glycosides are prepared. These glycosides are obtained from substantially
pure compounds according to Koeltzow and Urfer, supra. These compounds are referenced
in the syle of R
xDPy wherein R indicates the starting alcohol used to prepare the glycoside, x indicates
the chain length of the alcohol, and DP indicates that the material is a saccharide
having a degree of polymerization as indicated by y, e.g., DPi is glucose.
[0032] The following glucosides are obtained:
(a) C10DP1
(b) C12DP1
(c) C,3DP,
(d) C13DP,-(e) C15DP1
(f) C10DP2
(g) C12DP2
(h) C12DP3
* Obtained as a branched chain alcohol described as an isomeric mixture of branched
primary aliphatic alcohols containing carbon numbers predominantely in the range of
C11 through C,4 with C13 as the main constituent. The C12 content is approximately 20%. It boils in the approximate range of 250°C to 265°C
(482°F to 509°F). The alcohol is typically quite low in C" content (less than 2%); C14 content is estimated at 4%.
Example II
[0033] A base formulation of an anionic surfactant is prepared containing:

[0034] The pH of the base formula is adjusted and maintained from 5 to 5.5 with citric acid.
[0035] A series of comparative examples as described below are made by including the additive
from Example I into the base formula. The results are shown in Table I.

[0036] The above test uses as a standard cocoamide monoethanolamine which is a commonly
accepted viscosity control agent for liquid detergent products. Like all amines the
cocoamide monoethanolamine has a slightly objectionable odor. The products of this
invention are free of objectionable odors.
Example III
[0037] A base formula is prepared as indicated in Example II with the exception that the
additive is increased to 4% and the water in the formulation is decreased in a corresponding
amount. The oxo alcohol product
* gives a viscosity measurement of 3049. A control sample utilizes an equal amount
of Glucamate DOE-120 which is a methyl glucoside dioleate with 120 moles ethylene
oxide. The control gives a viscosity of 835. Glucamate DOE-120 is a Registered Trademark
of Amerchol Corporation, Edison N.J. USA.
Example IV
[0038] Substantially similar results are obtained in Example II when a similar amount of
a C
14 triethoxysulfate sodium salt is employed. Further, substitution for the olefin sulfonate
with a C
12 linear alkyl benzene sulfonate potassium salt gives substantially similar results.
1. A liquid detergent composition comprising:
(a) from 3% to 45% by weight of an anionic surfactant;
(b) from 0.3% to 20% by weight of monoglycoside represented as ROG wherein R is the
hydrophobic moiety (fatty organic portion) of the molecule containing from 10 to 24
carbon atoms, O is an oxygen, preferably in the 1 position of the saccharide, and
G represents the saccharide, and
(c) from 30% to 95% by weight of water,
and wherein the content, if any, of glucoside compounds having a degree of polymerization
(D.P.) of 2 or more within said composition is such that the average D.P. of all glycoside
compounds within said composition is less than 1.4.
2. A composition of Claim 1 wherein the anionic surfactant is selected from the group
consisting of alkyl sulfates, olefin sulfonates, paraffin sulfonates, alkyl benzene
sulfonates, alkyl ether sulfates, alkyl carboxylates, and mixtures thereof.
3. The composition of Claim 1 wherein the monoglycoside is a monoglucoside.
4. The composition of Claim 1 further containing a detergent builder.
5. The composition of Claim 4 wherein the detergent builder is a nitrilotriacetate
or phosphate salt.
6. The composition of Claim 1 or Claim 3 wherein the hydrophobic moiety of the monoglycoside
is derived from a branched alcohol.
* See Note Example I
7. The composition of Claim 1 additionally containing up to 10% by weight of an alkoxylated
nonionic surfactant.
8. The composition of any one of Claims 1, and 6, wherein the hydrophobic moiety is
derived from an oxo-alcohol structure.
9. The composition of any one of Claims 1 to 8 having a pH of from 5 to 8 when diluted
out on a dry solids basis to 0.1% by weight in water.
10. A method of increasing the viscosity of an aqueous liquid detergent composition
containing an anionic surfactant by including therein from 0.3% to 20% by weight of
an alkyl monoglycoside represented as ROG wherein R is the hydrophobic moiety (fatty
organic portion) of the molecule containing from 10 to 24 carbon atoms, O is an oxygen,
preferably in the 1 position of the saccharide, and G represents the saccharide, to
thicken the aqueous liquid detergent composition and by ensuring that the content,
if any, of glycoside compounds having a degree of polymerization (D.P.) of 2 or more
within said composition is such that the average D.P. of all glycoside compounds within
said composition is less than 1.4.
1. Flüssigwaschmittel enthaltend:
(a) 3 bis 45 Gew.-% eines anionischen Tensids,
(b) 0,3 bis 20 Gew.-% eines Monoglykosids der Formel ROG, in der R den hydrophoben
Teil des Moleküls (Fettalkylrest) mit 10 bis 24 Kohlenstoffatomen, O ein Sauerstoffatom,
vorzugsweise in 1-Stellung des Saccharids, und G das Saccharid bedeuten, und
(c) 30 bis 95 Gew.-% Wasser,
und wobei in diesem Mittel der Gehalt an Glykosidverbindungen mit einem Polymerisationsgrad
(D.P.) von 2 oder höher so gewählt ist, daß der Durchschnitts-D.P.-Wert aller Glkosidverbindungen
weniger als 1,4 beträgt.
2. Mittel nach Anspruch 1, in dem das anionische Tensid aus der Gruppe bestehend aus
Alkylsulfaten, Olefinsulfonaten, Paraffinsulfonaten, Alkylbenzolsulfonaten, Alkylethersulfaten,
Alkylcarboxylaten und Mischungen davon ausgewählt ist.
3. Mittel nach Anspruch 1, in dem das Monoglykosid ein Monoglucosid ist.
4. Mittel nach Anspruch 1, das zusätzlich eine Waschmittel-Buildersubstanz enthält.
5. Mittel nach Anspruch 4, in dem die Waschmittel-Buildersubstanz ein Nitrilotriacetat-
oder Phosphat-Salz ist.
6. Mittel nach Anspruch 1 oder 3, in dem der hydrophobe Teil des Monoglykosids von
einem verzweigten Alkohol abgeleitet ist.
7. Mittel nach Anspruch 1, das zusätzlich bis zu 10 Gew.-% eines alkoxylierten nichtionischen
Tensids enthält.
8. Mittel nach einem der Ansprüche 1, 3 and 6, in dem der hydrophobe Teil des Monoglykosids
von einer Oxoalkohol-Struktur abgeleitet ist.
9. Mittel nach einem der Ansprüche 1 bis 8, das, nach Verdünnung mit Wasser auf einen
Gehalt von 0,1 Gew.-%, bezogen auf eine trockene Feststoffbasis, einem pH-Wert von
5 bis 8 aufweist.
10. Verfahren zur Erhöhung der Viskosität eines wäßrigen Flüssigwaschmittels, das
ein anionisches Tensid enthält, durch Einarbeiten von 0,3 bis 20 Gew.-% eines Alkylmonoglykosids
der Formel ROG, in der R den hydrophoben Teil des Moleküls (Fettalkylrest) mit 10
bis 24 Kohlenstoffatomen, 0 ein Sauerstoffatom, vorzugsweise in 1-Stellung des Saccharids,
und G das Saccharid bedeuten, zum Verdicken des wäßrigen Flüssigwaschmittels, wobei
man den Anteil der Glykosidverbindungen mit einem Polymerisationsgrad (D.P.) von 2
oder mehr so einstellt, daß der Durchschnitts-D.P.-Wert aller Glykosidverbindungen
weniger als 1,4 beträgt.
1. Composition détergente liquide contenant:
a) de 3 à 45% en poids d'un tensio-actif anionique,
b) de 0,3 à 20% en poids d'un monoglycoside représenté par la formule ROG dans laquelle
R est la fraction hydrophobe (partie organique grasse) de la molécule contenant de
10 à 24 atomes de carbone, O est une atome d'oxygène placé, de préférence, en position
1 du saccharide et G représente le saccharide, et,
c) de 30 à 95% en poids d'eau et si la composition comporte des composés du type glycosides
ayant un degré de polymérisation (DP) au moins égal à deux, leur teneur dans celle-ci
est telle que le DP moyen de tous les composés du type glycosides dans la composition,
est inférieur à 1,4.
2. Composition selon la revendication 1 dans laquelle le tensio-actif anionique est
choisi dans le groupe constitué par les alcoylsulfates, les oléfinsulfonates, les
paraffinesulfonates, les alcoylbenzènesulfonates, les alcoyléthersulfates, les alcoylcarboxylates
et des mélanges de ceux-ci.
3. Composition selon la revendication 1, dans laquelle le monoglucoside est un monoglucoside.
4. Composition selon la revendication 1 contenant en outre un agent de structuration
de détergent.
5. Composition selon la revendication 4 dans laquelle l'agent de structuration de
détergent est un sel de nitrilotriacétate ou de phosphate.
6. Composition selon la revendication 1 ou la revendication 3 dans laquelle la fraction
hydrophobe du monoglycoside est dérivée d'un alcool ramifié.
7. Composition selon la revendication 1 contenant en supplément jusqu'à 10% en poids
d'un tensio-actif non ionique alcoxylé.
8. Composition selon l'une des revendications 1, et 6 dans laquelle la fraction hydrophobe
est dérivée d'une structure d'alcool-oxo.
9. Composition selon l'une des revendications 1 à 8 ayant un pH variant de 5 à 8 lorsqu'elle
est diluée à raison de 0,1% en poids de solide sec.
10. Procédé pour augmenter la viscosité d'une composition détergente liquide aqueuse
contenant un tensio-actif anionique par lequel on introduit dans celle-ci de 0,3 à
20% en poids d'un monoglycoside alcoylé représenté par la formule ROG dans laquelle
R est la fraction hydrophobe (partie organique grasse) de la molécule, qui contient
de 10 à 24 atomes de carbone, 0 est un atome d'oxygène placé de préférence en position
1 du saccharide et G représente le saccharide pour épaissir la composition détergente
liquide aqueuse et on fait en sorte que, si la composition comporte des composés du
type glycosides ayant un degré de polymérisation (DP) au moins égal à 2, leur teneur
dans celle-ci, est telle que le DP moyen de tous les composés du type glycosides dans
la composition soit inférieur à 1,4.