TECHNICAL FIELD
[0001] The present invention is related to liquid cleansing products, especially bath/shower
compositions which contain a cellulose polymer as a thickening/skin feel aid and a
solvent for viscosity control and phase stability.
BACKGROUND ART
[0002] The use of thickeners in liquid personal cleansing compositions is well known. U.S.
Pat. Nos. disclosing such compositions are 3,697,644, October 10, 1972 to Laiderman;
3,932,610, January 13, 1976 to Rudy et al.; 4,031,306, June 21, 1977 to DeMartino
et al.; and 4,061,602, December 6, 1977 to Oberstar et al.
[0003] It is also known that liquid personal cleansing products can be thickened by:
a. Using polymeric additives that hydrate, swell or molecularly associate to provide
body (e.g., hydroxy- propl guar gum is used as a thickening aid in shampoo compositions).
b. Using a combination of Carbopol (an acrylic acid polymer) and guar gum derivatives
(e.g., using combinations of Carbopol and Jaguar HP-60 gum/guar gum derivatives to
provide thickening and soft silky skin feel, as well as shelf stability).
c. Adding electrolytes, such as using NaCI to swell micelles to provide body.
[0004] While it is known to use thickeners in liquid cleansing compositions, there is no
teaching or suggestion of certain problems encountered with cellulose polymers in
making stable, good performing liquid cleansing bath/shower compositions, or solutions
thereto.
[0005] 'Specifically, there are no suggestions for incorporating the solvents used in this
invention into such compositions to obtain satisfactory stable products.
[0006] It is, therefore, an object of the present invention to provide cellulose polymers
containing liquid cleansing bath/shower compositions which are phase stable and cosmetically
attractive.
[0007] It is a further object of the present invention to provide liquid cleansing compositions
which are clear as well as stable.
[0008] it is still a further object of the present invention to provide liquid cleansing
compositions which deliver satisfactory skin feel and rinse properties.
[0009] These and other objects of the present invention will become obvious from the detailed
description which follows.
BRIEF DESCRIPTION OF THE FIGURE
[0010] The Figure shows four viscosity curves for five products vs. product concentration.
Curve 1 represents Example A; Curve 2 represents Example 11; Curve 3 represents Examples
1 (same as Example B) and 111; and Curve 4 Example C. The five product formulations
are found in the examples.
[0011] Curve 1 represents a product which has a high degree of slipperiness but is difficult
to rinse. Curves 2 and 3 represent products which have the desired degree of slipperiness
and ease of rinsing. Curve 4 represents a product which has a low degree of slipperiness,
but which is easy to rinse.
SUMMARY OF THE INVENTION
[0012] The present invention relates to liquid cleansing compositions comprising from about
0.1% to about 1.5% of a water-soluble cellulose polymer consisting of hydroxymethyl-,
hydroxyethyl-, hydroxypropyl-, hydroxybutyl methyl-, carboxymethyl cellulose, and
the like, from about 0.5% to about 20% of a solvent consisting of ethylene glycol
or propylene glycol (the monomers) or polyoxyethylene glycol or polyoxypropylene glycol
(considered as polymeric forms of ethylene glycol and propylene glycol, respectively)
or the mixed block copolymers of polyoxyethylene glycol and polyoxypropylene glycol
and mixtures thereof, from about 10% to about 50% of a synthetic surfactant, and from
about 50% to about 80% of water. The liquid cleansing composition has a neat (100%)
viscosity of 2,000-12,000 cps and a dilute (50%) viscosity of 15-95 cps. The compositions
must contain less then 1% electrolyte.
DETAILED DESCRIPTION OF THE INVENTION
[0013] An important attribute of a personal cleansing product is the feel of the product
in use. This feel can be described as soft, silky and slippery. Another important
attribute is the ease of rinsing of the product while in use. A poor rinsing product
can be described as one in which there is a prolonged feeling of slipperiness and
slickness during the rinsing process.
[0014] It has been discovered that the slipperiness and ease of rinsing of a product can
be related in part to the viscosity of the solution of the product in water as it
is diluted. This can be used to help describe products which have the desired level
of skin feel and ease of rinsing characteristics for certain end uses. The desired
product must then be formulated to provide the desired dilute viscosity curve which
controls skin feel and rinsing in use, the desired neat viscosity, the desired amount
of lather in use and a stable product that does not separate or change in neat viscosity
while stored.
[0015] It has been found that products with high dilution viscosity curves are desirable
to most women and disliked by most men because the product imparts a high degree of
slipperiness and silkiness, i.e., suitat
le for feminine use but not by both sexes. In addition, these products are difficult
to rinse for the same reasons. On the other hand, products that have low dilution
viscosity curves provide insufficient silky, slippery feel for both men and women,
but are very easy to rinse.
[0016] This invention relates to shelf stable products with desirable neat viscosity, using
selected thickeners, e.g., hydroxyethyl cellulose, and selected solvents, e.g., polyoxyethylene
or propylene glycol. The products are stable and provide a desirable level of skin
feel for both men and women by controlling the viscosity upon dilution relationships.
[0017] It is known to use Jaguar HP-60 polymer (hydroxypropyl guar gum, molar substitution
= 0.6) in a personal cleansing product. This provides a high dilution viscosity curve
desirable to most women and undesirable to most men. It is also known to use a combination
of Carbopol and Jaguar HP-60 and other guar gum derivatives which provide soft silky
skin feel that are shelf stable. These formulations though do not provide the desired
dilute viscosity and control of skin feel achieved in this development.
[0018] The terms "Neat Viscosity" and "Dilute Viscosity" as used herein are defined according
to the method taught herein, unless otherwise indicated.
Cellulosic Thickeners
[0019] The cellulosic thickeners in this invention are categorized as nonionic or anionic
and are selected to provide the desired viscosities. Suitable cellulosic thickeners
are listed in the Glossary and Chapters 3, 4, 12 and 13 of the Handbook of Water-Soluble
Gums and Resins, Robert L. Davidson, McGraw-Hill Book Co., New York, N.Y., 1980, incorporated
by reference herein.
[0020] The nonionic cellulosic thickeners include, but are not limited to, the following
polymers:
1. hydroxyethyl cellulose;
2. hydroxymethyl cellulose;
3. hydroxypropyl cellulose; and
4. hydroxybutyl methyl celulose.
[0021] The anionic cellulosic thickener includes carboxymethyl cellulose and the like.
[0022] The preferred thickener is hydroxyethyl cellulose, which is made by treating cellulose
with sodium hydroxide and reacting with ethylene oxide. Hydroxyethyl groups (molar
substitution 1.5 to 3, preferably 2 to 3) are introduced to yield a hydroxyethyl ether.
The reaction product is purified and ground to a fine white powder.
[0023] The amount of cellulosic thickener found useful in the present compositions is about
0.1% to about 1.5%, preferably from about 0.1% to about 1.0%. The thickeners are used
in combination with the solvent to produce the neat and dilute viscosities of 2,000
to 12,000 cps and 15 to 95 cps, respectively, preferably 4,000 to 10,000 cps and 20
to 60 cps, respectively.
Solvent
[0024] A second essential component of the present compositions is solvent consisting of
ethylene glycol or propylene glycol (the monomers) or polyoxyethylene glycol or polyoxypropylene
glycol (considered as a polymeric form of ethylene glycol or propylene glycol) or
the mixed block copolymers of polyoxyethylene glycol and polyoxypropylene glycol and
mixtures thereof. The polymeric forms of solvent have an average molecular weight
in the range of from about 200 to about 10,000, preferably 400 to 800. The solvent
is present at a level of from about 0.5% to about 20%, preferably from about 1% to
about 10% in the present compositions.
Surfactant
[0025] The third essential component of the present compositions is a surfactant. The surfactant,
which may be selected from any of a wide variety of anionic (nonsoap), amphoteric,
zwitterionic, nonionic and, in certain instances, cationic surfactants, is present
at a level of from about 10% to about 50%, preferably from about 10% to about 30%.
[0026] Anionic nonsoap surfactants can be exemplified by the alkali metal salts of organic
sulfuric reaction products having in their molecular structure an alkyl radical containing
from 8 to 22 carbon atoms and a sulfonic acid or sulfuric acid ester radical (included
in the term alkyl is the alkyl portion of higher acyl radicals). Preferred are the
sodium, ammonium, potassium or triethanolamine alkyl sulfates, especially those obtained
by sulfating the higher alcohols (C8-C18 carbon atoms), sodium coconut oil fatty acid
monoglyceride sulfates and sulfonates; sodium or potassium salts of sulfuric acid
esters of the reaction product of 1 mole of a higher fatty alcohol (e.g., tallow or
coconut oil alcohols) and 1 to 12 moles of ethylene oxide; sodium or potassium salts
of alkyl phenol ethylene oxide ether sulfate with 1 to 10 units of ethylene oxide
per molecule and in which the alkyl radicals contain from 8 to 12 carbon atoms, sodium
alkyl glyceryl ether sulfonates; the reaction product of fatty acids having from 10
to 22 carbon atoms esterified with isethionic acid and neutralized with sodium hydroxide;
water soluble salts of condensation products of fatty acids with sarcosine; and others
known in the art.
[0027] Nonionic surfactants can be broadly defined as compounds produced by the condensation
of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound,
which may be aliphatic or alkyl aromatic in nature. Examples of preferred classes
of nonionic surfactants are:
1. The polyethylene oxide condensates of alkyl phenols, e.g., the condensation products
of alkyl phenols having an alkyl group containing from about 6 to 12 carbon atoms
in either a straight chain or branched chain configuration, with ethylene oxide, the
said ethylene oxide being present in amounts equal to 10 to 60 moles of ethylene oxide
per mole of alkyl phenol. The alkyl substituent in such compounds may be derived from
polymerized propylene, diisobutylene, octane, or nonane, for example.
2. Those derived from the condensation of ethylene oxide with the product resulting
from the reaction of propylene oxide and ethylene diamine products which may be varied
in composition depending upon the balance between the hydrophobic and hydrophilic
elements which is desired. For example, compounds containing from about 40% to about
80% polyoxyethylene by weight and having a molecular weight of from about 5,000 to
about 11,000 resulting from the reaction of ethylene oxide groups with a hydrophobic
base constituted of the reaction product of ethylene diamine and excess propylene
oxide, said base having a molecular weight of the order of 2,500 to 3,000, are satisfactory.
3. The condensation product of aliphatic alcohols having from 8 to 18 carbon atoms,
in either straight chain or branched chain configuration with ethylene oxide, e.g.,
a coconut alcohol ethylene oxide condensate having from 10 to 30 moles of ethylene
oxide per mole of coconut alcohol, the coconut alcohol fraction having from 10 to
14 carbon atoms. Other ethylene oxide condensation products are ethoxylated fatty
acid esters of polyhydric alcohols (e.g., Tween 20-polyoxyethylene (20) sorbitan monolaurate).
4. Long chain tertiary amine oxides corresponding to the following general formula:

wherein R1 contains an alkyl, alkenyl or monohydroxy alkyl radical of from about 8 to about
18 carbon atoms, from 0 to about 10 ethylene oxide moieties, and from 0 to 1 glyceryl
moiety, and R2 and R3 contain from 1 to about 3 carbon atoms and from 0 to about 1 hydroxy group, e.g.,
methyl, ethyl, propyl, hydroxy ethyl, or hydroxy propyl radicals. The arrow in the
formula is a conventional representation of a semipolar bond. Examples of amine oxides
suitable for use in this invention include dimethyldodecylamine oxide, oleyldi(2-hydroxyethyl)
amine oxide, dimethyloctylamine oxide, dimethyl- decylamine oxide, dimethyltetradecylamine
oxide, 3,6,9- trioxaheptadecyldiethylamine oxide, di(2-hydroxyethyl)-tetradecylamine
oxide, 2-dodecoxyethyldimethylamine oxide, 3-dodecoxy-2-hydroxypropyldi(3-hydroxypropyl)-amine
oxide, dimethylhexadecylamine oxide.
5. Long chain tertiary phosphine oxides corresponding to the following general formula:

wherein R contains an alkyl, alkenyl or monohydroxyalkyl radical ranging from 8 to
18 carbon atoms in chain length, from 0 to about 10 ethylene oxide moieties and from
0 to 1 glyceryl moiety and R' and R" are each alkyl or monohydroxyalkyl groups containing
from 1 to 3 carbon atoms. The arrow in the formula is a conventional representation
of a semipolar bond. Examples of suitable phosphine oxides are: dodecyldimethylphos-
phine oxide, tetradecylmethylethylphosphine oxide, 3,6,9-trioxaoctadecyldimethylphosphine
oxide, cetyl- dimethylphosphine oxide, 3-dodecoxy-2-hydroxypropyl- di(2-hydroxyethyl)
phosphine oxide stearyldimethyl- phosphine oxide, cetylethylpropylphosphine oxide,
oleyldiethylphosphine oxide, dodecyldiethylphosphine oxide, tetradecyldiethylphosphine
oxide, dodecyldipro- pylphosphine oxide, dodecyldi(hydroxymethyl)phosphine oxide,
dodecyldi(2-hydroxyethyl)phosphine oxide, tetra- decylmethyl-2-hydroxypropylphosphine
oxide, oleyldi- methylphosphine oxide, 2-hydroxydodecyldimethylphos- phine oxide.
6. Long chain dialkyl sulfoxides containing one short chain alkyl or hydroxy alkyl
radical of 1 to about 3 carbon atoms (usually methyl) and one long hydrophobic chain
which contain alkyl, alkenyl, hydroxy alkyl, or keto alkyl radicals containing from
about 8 to about 20 carbon atoms, from 0 to about 10 ethylene oxide moieties and from
0 to 1 glyceryl moiety. Examples include: octadecyl methyl sulfoxide, 2-ketotridecyl
methyl sulfoxide, 3,6,9-trioxaoctadecyl 2-hydroxyethyl sulfoxide, dodecyl methyl sulfoxide,
oleyl 3-hydroxypropyl sulfoxide, tetradecyl methyl sulfoxide, 3-methoxytridecyl methyl
sulfoxide, 3-hydroxytridecyl methyl sulfoxide, 3-hydroxy-4-dodecoxybutyl methyl sulfoxide.
[0028] Zwitterionic surfactants can be exemplified by those which can be broadly described
as derivatives of aliphatic quaternary ammonium, phosphonium, and sulfonium compounds,
in which the aliphatic radicals can be straight chain or branched and wherein one
of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains
an anionic water-solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate,
or phosphonate. A general formula for these compounds is:

wherein R contains an alkyl, alkenyl, or hydroxy alkyl radical of from about 8 to
about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties and from 0 to 1
glyceryl moiety; Y is selected from the group consisting of nitrogen, phosphorus,
and sulfur atoms; R
3 is an alkyl or monohydroxyalkyl group containing 1 to about 3 carbon atoms; X is
1 when Y is a sulfur atom and 2 when Y is a nitrogen or phosphorus atom; R
4 is an alkylene or hydroxyalkylene of from 1 to about 4 carbon atoms and Z is a radical
selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate,
and phosphate groups.
[0029] Examples include: 4-[N,N-di(2-hydroxyethyl)-N-octadecyl- ammonio]-butane-1-carboxylate;
5-[S-3-hydroxypropyl-S-hexade- cylsulfonio]-3-hydroxypentane-1-sulfate; 3-[P,P-P-diethyl-P-3,6,
9-trioxatetradexocylphosphonio]-2-hydroxypropane-1-phosphate; 3- [N,N-dipropyl-N-3-dodecoxy-2-hydroxypropylammonio]-propane-1-phosphonate;
3- (N, N-dimethyl-N-hexadecylammonio)propane-1-sulfonate; 3-(N,N-dimethyl-N-hexadecylammonio)-2-hydroxypropane-1-sulfonate;
4-[N,N-di(2-hydroxyethyl)-N-(2-hydroxydode- cyl)ammonio]-butane-1-carboxylate; 3-[S-ethyl-S-(3-dodecoxy-2-hydroxypropyl)sulfonio]-propane-1-phosphate;
3-(P,P-dimethyl-P-dodecytphosphonio)-propane-1-phosphonate; and 5-[N,N-di(3-hydroxypropyl)-N-hexadecylammonio]-2-hydroxy-pentane-1-sulfate.
[0030] Examples of amphoteric surfactants which can be used in the compositions of the present
invention are those which can be broadly described as derivatives of aliphatic secondary
and tertiary amines in which the aliphatic radical can be straight chain or branched
and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon
atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfonate,
sulfate, phosphate, or phosphonate. Examples of compounds falling within this definition
are sodium 3-dodecylaminopropionate, sodium sodium 3-dodecylaminopropane sulfonate,
N-alkyltaurines, such as the one prepared by reacting dodecylamine with sodium isethionate
according to the teaching of U.S. Pat. No. 2,658,072, N-higher alkyl aspartic acids,
such as those produced according to the teaching of U.S. Pat. No. 2,438,091, and the
products sold under the trade name "Miranol" and described in U.S. Pat. No. 2,528,378.
Other amphoterics such as betaines are also useful in the present composition.
[0031] Examples of betaines useful herein include the high alkyl betaines such as coco dimethyl
carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxyethyl
betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis-(2-hydroxyethyl)carboxy
methyl betaine, stearyl bis-(2-hydroxypropyl) carboxymethyl betaine, oleyl dimethyl
gamma-carboxypropyl betaine, lauryl bis-(2-hydroxypropyl) alpha-carboxyethyl betaine,
etc. The sulfo-betaines may be represented by coco dimethyl sulfopropyl betaine, stearyl
dimethyl sulfopropyl betaine, lauryl bis-(2-hydroxyethyl) sulfopropyl betaine, amido
betaines amidosulfobetaines, and the like.
[0032] Many cationic surfactants are known to the art. By way of example, the following
may be mentioned:
stearyldimethylbenzyl ammonium chloride;
dodecyltrimethylammonium chloride;
nonylbenzylethyldimethyl ammonium nitrate;
tetradecylpyridinium bromide;
laurylpyridinium chloride;
cetylpyridinium chloride;
laurylpyridinium chloride;
laurylisoquinolium bromide;
ditallow(hydrogenated)dimethyl ammonium chloride;
dilauryldimethyl ammonium chloride; and
stearalkonium chloride.
[0033] Many additional nonsoap surfactants are described in McCUTCHEON'S, DETERGENTS AND
EMULSIFIERS, 1979 ANNUAL, published by Allured Publishing Corporation, which is incorporated
here by reference.
[0034] The above-mentioned surfactants can be used in the liquid cleansing bath/shower compositions
of the present invention. The anionic surfactants, particularly the alkyl sulfates,
the ethoxylated alkyl sulfates and mixtures thereof are preferred. More preferred
are anionic surfactants selected from the group consisting of sodium alkyl glycerol
ether sulfonate, sodium lauroyl sarcosinate, sodium alkyl sulfate, sodium ethoxy (3)
alkyl sulfate, and mixtures thereof.
Electrolyte
[0035] An additional requirement of the present compositions is that they contam a low level
of electrolyte. Electrolytes include inorganic salts (e.g., sodium chloride) as well
as organic salts (e.g., sodium citrate). The amount of electrolyte varies with the
type of surfactant but should not be present in finished product at a level greater
than 1.0%, preferably as little as possible and less than 0.5%. In addition to the
above-mentioned chloride and citrate salts, other salts include phosphates, sulfates
and other halogen ion salts. The counter ions of such salts can be sodium or other
monovalent cations as well as di- and trivalent cations. It is recognized that these
salts may cause instability if present at greater than 1.0% levels.
Aqueous Carrier
[0036] The liquid cleansing bath/shower compositions herein are in the form of liquids in
which water is the principal diluent. The level of water in the compositions is typically
from about 50% to about 80%.
Optional Components
[0037] The liquid cleansing bath/shower compositions can contain a variety of nonessential
optional ingredients suitable for rendering such compositions more desirable. Such
conventional optional ingredients are well known to those skilled in the art, e.g.,
preservatives such as benzyl alcohol, methyl paraben, propyl paraban and imidazolidinyl
urea; other thickeners and viscosity modifiers such as C
S-C
1S ethanolamide (e.g., coconut ethanolamide) and polyvinyl alcohol; skin moisturizers
such as glycerine; pH adjusting agents such as citric acid, succinic acid, phosphoric
acid, sodium hydroxide, etc.; suspending agents such as magnesium/aluminum silicate;
perfumes; dyes; and sequestering agents such as disodium ethylendiamine tetraacetate.
[0038] One preferred form of the present compositions is a clear product. However, if desired,
a pearlescer such as ethylene glycol distearate may be used to give the product a
pearlescent effect.
[0039] A preferred liquid cleansing product contains from about 1% to about 5% of an alkanolamide
of a fatty acid having from about 8 to about 18 carbon atoms.
[0040] If present, the optional components individually generally comprise from about 0.001%
to 10.0% by weight of the composition. The pH of the liquid cleansing bath/shower
compositions herein is generally from about 3 to about 9, preferably from about 5
to about 8.
Method of Manufacture
[0041] The liquid cleansing compositions of the present invention may be made using techniques
well known in the art. A suitable method is shown in Example I.
Industrial Applicability
[0042] The liquid cleansing compositions are useful as a cleansing aid for the entire body.
The basic invention of a cellulose polymer thickener and solvent may also be applicable
in other liquid type products such as liquid hand soaps and light duty dishwashing
liquids that require a certain degree of skin feel.
Method I - Neat Viscosity (100% Product)
Operation: (Brookfield LVF-Type Viscometer)
[0043] Pour approximately 140g of the finished product into a 150 ml beaker taking care
to avoid trapping air bubbles. Check the product temperature with the thermometer
- the temperature should be between 74.5-75.5°F. If not, a warm water or a cold water
bath must be used to adjust the temperature. A common galvanized laboratory tray (depth
of approximately 21 inches) may be used. Temperatures of the baths should be 60-65°F
for the cold and 85-90°F for the warm water. Place the beaker in the bath and stir
sample gently with the thermometer, taking care to avoid generation of air bubbles.
The sample is ready for analysis when a uniform temperature of 74.5-75.5
0F exists throughout the sample. Attach spindle #4 to the viscometer. While the temperature
of the sample is within the limits, carefully lower viscometer spindle #4 into the
beaker. The spindle guard should not be attached. (Note: It is important that the
spindle temperature is equilibrated to room temperature before inserting into the
sample; allow at least 15 minutes for temperature equilibration after washing spindle.)
Do not lower the spindle below the depth notch. If this occurs, raise the spindle
and carefully wipe the shaft above the notch, then reinsert the spindle into the sample.
Center the spindle in the beaker with the surface of the sample in the center of the
spindle depth notch. Start the viscometer motor, set at 30 rpm's, wait 15 seconds,
then take a meter reading. Take two additional readings. Refer to the Brookfield viscometer
manual for proper operation.
Calculations:
[0044] Calculate the viscosity of the sample as follows:
A = Average of the three meter readings.
200 = Conversion factor found in the Brookfield manual for spindle #4 @ 30 rpm's.
[0045] NOTE: When reporting the viscosity of the solution, always include the temperature
74.5-75.5°F (23.6-24.2°C).
Method II - Dilute Viscosity
(50% Product/50% Water)
Operation: (Brookfield LVF-Type Viscometer)
[0046] Pour 175g of finished product and 175g of distilled water into a 400 ml beaker. Mix
by hand with stirring rod taking care to avoid air bubbles. Check the solution temperature
with the thermometer - the temperature should be between 74.5-75.5°F. If not, a warm
water or a cold water bath must be used to adjust the temperature. A common galvanized
laboratory tray (depth of approximately 2i inches) may be used. Temperatures of the
baths should be 60-65°F for the cold and 85-90°F for the warm water. Place the beaker
in the bath and stir sample gently with the thermometer, taking care to avoid generation
of air bubbles. The sample is ready for analysis when a uniform temperature of 74.5-75.5°F
exists throughout the sample. Attach spindle #I to the viscometer. While the temperature
of the sample is within the limits, carefully lower viscometer spindle #I in the beaker.
The spindle guard should not be attached. (Note: It is important that the spindle
temperature is equilibrated to room temperature before inserting into the sample;
allow at least 15 minutes for temperature equilibration after washing spindle.) Do
not lower the spindle below the depth notch. If this occurs, raise the spindle and
carefully wipe the shaft above the notch, then reinsert the spindle into the sample.
Center the spindle in the beaker with the surface of the sample in the center of the
spindle depth notch. Start the viscometer motor, set at 30 rpm's, wait 15 seconds,
then take a meter reading. Take two additional readings. Refer to the Brookfield viscometer
manual for proper operation.
Calculations:
[0047] Calculate the viscosity of the sample as follows:
A = Average of the three meter readings
2 = Conversion factor found in the Brookfield manual for spindle #1 @ 30 rpm's.
[0048] NOTE: When reporting the viscosity of the solution, always include the temperature,
74.5-75.5°F (23.6-24.2°C).
EXAMPLES
[0049] The following examples further describe and demonstrate the preferred embodiments
within the scope of the present invention. The Examples are given solely for the purpose
of illustration and are not to be construed as limitations of the present invention
as many variations thereof are possible without departing from its spirit and scope.
Unless otherwise indicated, all percentages and ratios herein are by weight.
[0050] In addition to the examples is a Skin Feel Test Procedure and the results thereof
(Tables 1 and 2) that demonstrate the differences in both in-use slipperiness and
ease of rinsing for HEC-thickened products vs. Jaguar and salt-thickened products.
Skin Feel Test (Forearms)
Procedure:
[0051] Pre-Wash. Panelists were asked to first wash both forearms using CAMAY toilet bar
soap. After rinsing, while the arms were still wet, an initial skin friction reading
(using a Skin Friction Meter, Ser. No. 595108, made by the Department of Engineering,
University of Newcastle, Newcastle, England) was made on both forearms. Two syringes
were then filled with 1.0 ml of two of the three products to be tested.
[0052] In-Use Slipperiness. With arms still wet, the first product was delivered to the
palm of the right hand. The product was then rubbed on the underside of the left forearm
for 10 strokes (1 stroke is defined as rubbing the forearm from the wrist to the inside
crease of the elbow and back to the wrist). The second product was immediately delivered
to the left palm and rubbed on the underside of the right arm for 10 strokes. At this
point, a skin friction reading was taken with the products still on the arms. Results
are shown in Table 1.
[0053] Ease of Rinsing. Panelists were then asked to rinse each arm separately, counting
the number of bare hand strokes needed to completely rinse the product off their forearms.
Results are shown in Table 2.
TABLE 1
Skin Friction Meter Results
(In-Use Slipperiness)
[0054] Skin friction data of product on skin correlate with expected in-use slipperiness
based on the skin feel agents used in the following products. Examples A, B and C
listed below describe the three formulas used in this test.

[0055] The Neat and Dilute Viscosities of the above liquid cleansers, Examples A, B and
C, are shown in the Figure as Curves 1, 3 and 4, respectively. The skin friction reduction
results are as follows:

[0056] The confidence levels of significant differences (using the Student T test) between
the three products are as follows:

TABLE 2
Panelist Rinsing Results
(Ease of Rinsing)
[0057] Panelist product rinsing results correlate with expected ease of rinsing. The results
are as follows:

[0058] NOTE: Above results are based on a complete round robin paired comparison test using
a base panel of 22-23 for each pair tested.
[0059] The confidence levels of significant differences between the three products are as
follows:

EXAMPLE I
[0060] A full product formula was made with 0.2% hydroxyethyl cellulose (HEC) and 3% propylene
glycol. The base formulation used in this variation contained the following ingredients:

[0061] The above composition was prepared in the following manner:
- A cold (room temperature) mix was prepared by adding ingredients in the following
order: 50% of the added distilled water, hydroxyethyl cellulose, sodium lauryl ethoxy
(3) sulfate solution and 50% of the sodium lauryl sulfate solution.
- A hot (60-71.1°C, 140-160°F) mix was prepared by adding ingredients in the following
order: 50% of the added distilled water, 50% of the sodium lauryl sulfate solution,
ethylene diamine tetraacetic acid, preservatives, coconut monoethanolamide, propylene
glycol and ethylene glycol distearate.
- The hot mix was poured into the cold mix, with agitation.
- The remaining ingredients were mixed in the following order: color solution, citric
acid and perfume.
EXAMPLE II
[0062] A second full product formula was made with 0.5% hydroxyethyl cellulose (HEC) and
5% propylene glycol. The base formulation used in this variation contained the following
ingredients:

[0063] The above composition of the present invention was prepared in a manner similar to
that described in Example I.
EXAMPLE III
[0064] A third full product formula was made with 0.2% hydroxyethyl cellulose (HEC) and
2% polyoxyethylene glycol (PEG 600). The base formula used in this variation contained
the following ingredients:

[0065] The above composition of the present invention was prepared in a manner similar to
that described in Example I.
[0066] Examples I-III demonstrated the following regarding in-use skin feel slipperiness
and rinsing characteristics using the Skin Feel Test:
1. No difference in slip or ease of rinsing between the three HEC formulas of Examples
I-III.
2. Less slip and easier to rinse than a similar formula, Example A, which has 0.55%
Jaguar HP-60 gum.
3. More slip and harder to rinse than formula thickened with electrolyte (NaCI), Example
C.
[0067] The Figure shows plots of viscosity vs. dilute concentration curves with noted product
skin feel attributes. As can be seen, the three HEC formula dilution curves are similar
and fall in between the highly slick/slippery formula thickened with Jaguar gum Example
"A" and the less slick/slippery competitive formula thickened with electrolyte Example
"C". Curve 1 represents a product, Example A, which has a high degree of slipperiness
but is difficult to rinse. Curves 2 and 3 represent products, Examples II and I/III,
respectively, which have the desired degree of slipperiness and ease of rinsing. Curve
4 represents a product, Example C, which has a low degree of slipperiness, but which
is easy to rinse. See Methods I and 11 for neat and dilute viscosity procedures.
EXAMPLES IV & V
[0068] These examples illustrate the need for a solvent, in this case propylene glycol,
to achieve phase stability. Two full product formulations were prepared, one (IV)
with 0% propylene glycol and the other (V) with 3% propylene glycol. The base formulation
used in these variations contained the following ingredients:

[0069] The above compositions of the present invention were prepared in a manner similar
to that described in Example 1.
[0070] Results showed the non-propylene glycol-containing formula (IV) had phase separation
after only a few days; whereas the propylene glycol formula (V) of this invention
remained phase stable for several months.