U.S. patent number 3,920,561 [Application Number 05/488,338] was granted by the patent office on 1975-11-18 for composition for imparting softness and soil release properties to fabrics.
This patent grant is currently assigned to The Procter & Gamble Company. Invention is credited to Thomas Allen DesMarais.
United States Patent |
3,920,561 |
DesMarais |
November 18, 1975 |
Composition for imparting softness and soil release properties to
fabrics
Abstract
Fabric treating compositions comprising a fabric softener and a
highly substituted methyl cellulose derivative confer softness and
soil release properties to fabrics.
Inventors: |
DesMarais; Thomas Allen
(Cincinnati, OH) |
Assignee: |
The Procter & Gamble
Company (Cincinnati, OH)
|
Family
ID: |
23939343 |
Appl.
No.: |
05/488,338 |
Filed: |
July 15, 1974 |
Current U.S.
Class: |
510/517;
427/393.4; 427/393.1 |
Current CPC
Class: |
C11D
3/225 (20130101); C11D 1/62 (20130101); D06M
15/09 (20130101); C11D 3/0036 (20130101) |
Current International
Class: |
C11D
3/00 (20060101); C11D 3/22 (20060101); D06M
15/09 (20060101); C11D 1/38 (20060101); D06M
15/01 (20060101); C11D 1/62 (20060101); D06M
015/24 () |
Field of
Search: |
;252/8.8,8.9,542,547,545
;117/139C,139F ;260/231CM |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Czaja; Donald E.
Assistant Examiner: Woodberry; Edward
Attorney, Agent or Firm: Yetter; Jerry J. Schaeffer; Jack D.
Witte; Richard C.
Claims
What is claimed is:
1. A fabric treating composition comprising:
a. from about 1 to about 50% by weight of a combined fabric
softening and anti-static agent;
b. from about 0.05 to about 10% by weight of a methyl cellulose
ether having a DS methyl of at least about 2.1, a weight average
degree of polymerization of greater than about 100, a solution
viscosity above about 20 centipoise and a gel point less than about
50.degree.C; and
c. the balance of the composition comprising a water-dispersible
carrier.
2. A composition according to claim 1 wherein the fabric softening
and anti-static agent is selected from the group consisting of
quaternary ammonium salts containing at least one C.sub.10
-C.sub.20 fatty alkyl substituent group; alkyl imidazolinium salts
wherein at least one alkyl group contains a C.sub.8 -C.sub.25
carbon chain; and C.sub.12 -C.sub.20 alkyl pyridinium salts.
3. A composition according to claim 2 wherein the quaternary
ammonium salt is of the formula R.sup.1 R.sup.2 R.sup.3 R.sup.4
N.sup.+, X.sup.-, wherein R.sup.1 and R.sup.2 are each C.sub.12
-C.sub.20 fatty alkyl groups, or mixtures thereof, and R.sup.3 and
R.sup.4 are each C.sub.1 -C.sub.3 alkyl groups, or mixtures
thereof, and wherein X is an anion.
4. A composition according to claim 3 wherein the quaternary
ammonium salt is selected from ditallowalkyldimethylammonium
chloride and dicoconutalkyldimethylammonium chloride.
5. A composition according to claim 1 wherein the methyl cellulose
ether has a DS methyl of from about 2.1 to about 2.8.
6. A composition according to claim 5 wherein the DS methyl is 2.2
to 2.7.
7. A composition according to claim 1 comprising a quaternary
ammonium salt selected from ditallowalkyldimethylammonium chloride
and dicoconutalkylammonium chloride and a methyl cellulose ether
characterized by a DS methyl from about 2.3 to about 2.6.
8. A composition according to claim 7 comprising from about 3 to
about 15% by weight of the quaternary ammonium salt, from about
0.25 to about 2.0% by weight of the methyl cellulose ether,
characterized by a viscosity in the range from about 20 cps to
about 250 cps, the balance of the composition comprising a liquid
carrier selected from water and mixtures of water and lower
alcohols.
9. A composition according to claim 8 comprising, as an additional
component, a non-deterging amount of a nonionic surfactant, or
mixtures thereof.
10. A composition according to claim 9 wherein the surfactant is
selected from ethoxylated alcohols and ethoxylated phenols
characterized by a hydrophilic-lipophilic balance in the range of
about 7 to about 15 or mixtures thereof.
Description
BACKGROUND OF THE INVENTION
This invention relates to fabric treating compositions and to a
method for simultaneously softening and imparting soil release
properties to textile materials. More specifically, the
compositions herein comprise mixtures of a fabric softener such as
the common cationic ammonium softeners, and specific, highly
substituted methyl cellulose soil release agents.
It is common practice to soften fabrics during the rinse cycle of a
laundering operation. Fabric "softness" is an expression
well-defined in the art and is usually understood to be that
quality of the treated fabric whereby its handle or texture is
smooth, pliable and fluffy to the touch. Various chemical compounds
have long been known to possess the ability to soften fabrics
during a laundering operation. The use of various surface modifying
or coating agents to improve the cleaning properties of fabrics is
also a well known technique. Much effort has been expended in
designing various compounds capable of conferring soil release
properties to fabrics, especially those woven from polyester
fibers. The hydrophobic character of polyester fabrics makes their
laundering (particularly as regards oily soil and oily stains)
difficult, principally due to the low wettability of the polyester
fibers. Since the inherent character of the fiber itself is
hydrophobic, or oleophilic, once an oily soil or oily stain is
deposited on the fabric it tends to be "attached" to the surface of
the fiber. As a result, the oily soil or stain is difficult to
remove in an aqueous laundering process.
When hydrophilic fabrics such as cotton are soiled by oily stains
or oily soil, it is well-recognized that the oil is much more
easily removed than in the case of hydrophobic polyester fabrics.
This difference in oil removal characteristics is apparently caused
by the greater affinity of cotton fabrics for water. Differences in
hydrophilic/hydrophobic characteristics of cotton and polyester are
due in part to the basic building blocks of the fibers themselves.
That is, since polyester fibers are usually polymers of
terephthalic acid and ethylene glycol, they have less affinity for
water because there are fewer free hydrophilic groups, e.g.,
hydroxyl or carboxyl groups, where hydrogen bonding can occur. With
cotton, which is a cellulosic material, the large number of
hydrophilic groups provides compatibility with, and affinity for,
water.
From a detergency standpoint, the most important difference between
hydrophobic fabrics and hydrophilic fabrics is the tendency for
oily soil to form easily removable droplets when present on a
hydrophilic fabric and in contact with water. The mechanical action
of washing and the action of synthetic detergents and builders
normally used in the washing step of the laundering process removes
such oil droplets from the fabrics. The droplet formation is in
contrast to the situation which exists with polyester (hydrophobic)
fibers. Water does not "wick" through hydrophobic fabrics and the
oily soil or stain tends to be retained throughout the fabric, both
because of the inherent hydrophobic character of the fabric and the
lack of affinity of oily soil for water. Since all fabrics, and
especially polyester and polyester-blend fabrics (e.g.,
polyester-cotton blends) are susceptible to oily staining and, once
stained, are difficult to clean in an aqueous laundry bath,
manufacturers of such fibers and fabrics have sought to increase
their hydrophilic character to provide ease of laundering.
A truly superior fabric treating agent should provide a soft,
desirable hand to the fabric, as well as a soil release finish.
Moreover, an optimal fabric treating agent should also provide
anti-static benefits. To many users, "softness" connotes the
absence of static cling in the fabrics. Indeed, with fabrics such
as nylon and polyester, many users appreciate an anti-static
benefit at least as much as a softening benefit.
As might be expected, a wide variety of materials have been
suggested for use as fabric and textile conditioning agents to
provide one or more of the foregoing benefits. In many instances,
such compositions are designed for use in processes carried out by
the fiber or textile manufacturer; see Netherlands Application
65/09456; see also Garrett and Hartley, J. Soc. Dyers and
Colourists, 82, 7, 252-7 (1967) and Chem. Eng. News, 44, 42-43
(Oct. 17, 1966). These references, as well as British Pat. Nos.
1,088,984 and 1,092,453, teach various ester-based soil release
agents.
U.S. Pat. Nos. 3,668,000; 3,435,027; 2,663,989; 2,994,665;
3,523,088; South African Pat. No. 71/5149; British Pat. Nos.
1,171,877 and 1,045,197; the "CELLULOSE GUM CATALOG", Hercules
Powder Company; and the "METHOCEL PRODUCT INFORMATION" data sheets,
Dow Chemical Company, 1966, disclose the use of a wide variety of
cellulose derivatives as fabric finishes.
U.S. Pat. No. 3,712,873 discloses textile treating compositions
comprising a quaternary ammonium softening compound and various
cellulose and/or modified starch derivatives in combination with a
variety of adjunct materials.
The co-pending application of DesMarais, entitled "DETERGENT
COMPOSITIONS HAVING IMPROVED SOIL RELEASE PROPERTIES", Ser. No.
462,700, filed Apr. 22, 1974, the disclosures of which are
incorporated herein by reference, relates to detergent compositions
containing highly substituted methyl cellulose derivatives of the
type employed herein.
It is an object of the present invention to provide combined
softening/soil release compositions which impart superior soil
release benefits, especially to polyester fabrics.
It is another object herein to provide compositions for
simultaneously imparting softness, anti-static benefits and soil
release properties to fabrics in one-step, home laundry rinse
bath.
The foregoing objects are obtained by combining a fabric
softening/anti-static agent and a methyl cellulose soil release
agent having a high degree of substitution (DS) in compositions of
the type disclosed hereinafter.
SUMMARY OF THE INVENTION
The present invention encompasses fabric treating compositions
comprising from about 1 to about 50% by weight of a combined fabric
softening and anti-sattic agent, from about 0.05 to about 10% by
weight of a methyl cellulose ether having a DS methyl of at least
about 2.1 and a gel point less than about 50.degree.C, the balance
of the composition comprising a water dispersible carrier,
especially liquid carriers such as water or water-alcohol
mixtures.
DETAILED DESCRIPTION OF THE INVENTION
Fabric Softener
The fabric softener employed in the present invention comprises any
of the cationic (including imidazolinium) compounds listed in U.S.
Pat. No. 3,686,025, incorporated herein by reference. Such
materials are well-known in the art and include, for example, the
quaternary ammonium salts having at least one, preferably two,
C.sub.10 -C.sub.20 fatty alkyl substituent groups; alkyl
imidazolinium salts wherein at least one alkyl group contains a
C.sub.8 -C.sub.25 carbon "chain"; the C.sub.12 -C.sub.20 alkyl
pyridinium salts, and the like.
Preferred softeners herein include the cationic quaternary ammonium
salts of the general formula R.sup.1 R.sup.2 R.sup.3 R.sup.4
N.sup.+, X.sup.-, wherein groups R.sup.1, R.sup.2, R.sup.3 and
R.sup.4 are, for example, alkyl and X.sup.- is an anion, e.g.,
halide, methylsulfate, and the like. Especially preferred softeners
herein are those wherein R.sup.1 and R.sup.2 are each C.sub.12
-C.sub.20 fatty alkyl and R.sup.3 and R.sup.4 are each C.sub.1
-C.sub.3 alkyl (or mixtures). The fatty alkyl groups can be mixed,
i.e., the mixed C.sub.14 -C.sub.18 coconutalkyl and mixed C.sub.16
-C.sub.18 tallowalkyl quaternary compounds. Alkyl groups R.sup.3
and R.sup.4 are preferably methyl. Useful quaternary ammonium
compounds herein are set forth in detail in U.S. Pat. No.
3,686,025.
Particularly useful quaternary ammonium softeners herein include
ditallowalkyldimethylammonium chloride and
dicoconutalkyldimethylammonium chloride.
Soil Release Agent
The soil release fabric finishing agents employed in the instant
compositions are the methyl ethers of cellulose having a high
degree of methyl substitution (DS). More specifically, the high DS
methyl cellulose ethers herein can be characterized as cellulose
having at least 2.1, preferably from about 2.1 to about 2.8, methyl
groups , R', on the hydroxyls of the anhydroglucose units of
cellulose, i.e., a DS of from 2.1 to 2.8. It has now been
discovered that these high DS methyl cellulose derivatives exhibit
heretofore unrecognized advantages as oily soil release fabric
finishes and are far superior to the lower DS methyl and the
various hydroxyalkyl cellulosics known in the art.
The basic structure of the cellulose methyl ethers herein is as
follows, wherein group R' is methyl. In the formula the integer, n,
typically averages from about 100 to about 10,000. ##SPC1##
When preparing the methyl cellulose ether soil release agents
employed in the present compositions the hydroxyl groups of the
anhydroglucose units of cellulose are reacted with a methylating
agent, thereby replacing the hydrogen of the hydroxyls with methyl.
The number of substituent methyl groups can be designated by weight
percent, or by the average number of methyl (i.e., as methoxyl)
groups on the anhydroglucose units, i.e., the DS. If all three
available positions on each anhydroglucose unit are substituted,
the DS is designated three (3); if an average of two --OH's are
substituted, the DS is designated two (2), etc.
Commercial processes for preparing methyl cellulose ethers involve,
for example, simply combining methyl chloride with a cellulose feed
stock of the type disclosed hereinafter under alkaline conditions.
(It is to be understood that the methyl halides used to prepare the
high DS methyl celluloses herein can contain minor amounts of other
alkyl halides. The resulting cellulose ethers may, of course,
contain very minor proportions of the corresponding alkyl groups.
This is not important to the invention herein.) Such a process
results in a DS below, 2, and most generally a DS of about 1.5. The
prior art materials taught for use as fabric finishes are those
having a low DS, i.e., a DS below 2, and usually below about 1.5.
These lower DS materials are apparently specified for use as fabric
finishes inasmuch as they are commercially available and have what
was heretofore thought to be the requisite high water solubility
necessary for sorption on fabric surfaces.
in contrast with the prior art teachings regarding the cellulosic
fabric finishes, the soil release agents for use herein have a
degree of methyl substitution in the range of from about 2.1 to
about 2.8, preferably from about 2.2 to about 2.7, most preferably
from about 2.3 to about 2.6.
Of course, the theoretical DS limit is 3.0, inasmuch as there are a
maximum of 3 hydroxyl groups on each anhydroglucose unit in
cellulose. Surprisingly, the high DS methyl cellulose ethers herein
are sufficiently water soluble to provide good soil release fabric
finishes when applied from an aqueous bath. Moreover, the high DS,
methyl cellulose ethers exhibit their superior oily soil release
properties when applied to fabrics from an aqueous rinse bath
containing the above-disclosed softening agents.
The high DS methyl cellulose ethers herein can be prepared by the
exhaustive methylation of cellulose using a methyl halide,
preferably methyl chloride, and caustic, preferably sodium
hydroxide, in a pressure vessel in the manner well-known in the art
for preparing the lower DS methyl cellulosics. However, the
methylation procedure can be simply repeated and continued until
the high DS materials are secured. The progress of the methylation
reaction can be monitored by periodically sampling the reaction
product and determining the degree of methoxylation in the manner
more fully disclosed hereinafter.
It is to be understood that fabric treating compositions containing
any of the high DS methyl cellulose materials disclosed herein
provide excellent oily soil removal finishes compared with most low
DS (i.e., DS below about 2) alkyl and hydroxyalkyl cellulosics
known in the art. For truly superior performance in this regard,
the most highly preferred high DS methyl cellulose ethers are those
which are characterized by a gel point in an aqueous solution below
about 50.degree.C, preferably in a range of from 25.degree. to
about 48.degree.C. While not intending to be limited by theory, it
appears that the high DS methyl cellulosics having gel points below
about 50.degree.C, and preferably in the recited range, interact
with, and deposit on, fabrics from an aqueous rinse bath in optimal
fashion under household conditions. The gel point of the cellulose
soil release ethers herein can be determined in the manner
disclosed more fully hereinafter.
The highly preferred methyl cellulosics for use herein are
characterized by their high DS and gel point as specified
hereinabove, and can be further characterized by a solution
viscosity above about 20 centipoise, more preferably above about 40
centipoise (cps). It is to be recognized that the solution
viscosities of the cellulose ethers herein can vary over an
extremely wide range, and are often as high as 70,000 (measured as
a 2% wt. solution in water). Typical solution viscosities of the
high DS methyl cellulose ethers range from about 90 to about
69,000, but cellulosics having viscosities falling outside this
range are useful herein, provided they have the high DS methyl
substitution and the specified gel points. The viscosity of the
preferred cellulosic derivatives herein can be determined in the
manner set forth in ASTM Standard D-2363, more fully described
hereinafter.
While any of the high DS cellulose ethers herein are useful in
granular compositions which can be prepared using solid,
water-soluble carriers such as sodium sulfate, sodium carbonate,
and the like, most fabric treating compositions are marketed as
liquids. When such liquid compositions are being prepared, it is
preferred to select ethers having viscosities in the lower end of
the range in order to maintain optimal flow and pouring properties.
Accordingly, when formulating liquid fabric treating compositions
with the cellulosic soil release agents in the manner of the
present invention, it is preferred to select cellulosics having a
solution viscosity (as a 2% wt. aqueous solution) from about 20 cps
to about 250 cps.
In addition to the foregoing parameters, the most highly preferred
high DS methyl cellulosics can be further characterized as having a
weight average degree of polymerization of greater than about 100,
more preferably from about 100 to about 1000, most preferably from
about 400 to about 800. The term "weight average degree of
polymerization" used herein to define the most highly preferred
high DS methyl cellulosics relates to the average number of
anhydroglucose units in the cellulose polymer. The weight average
degree of polymerization (DP.sub.W) is related to such physical
parameters of the cellulose polymer as solubility, gel point and
viscosity. The DP.sub.W of the high DS methyl cellulosics herein
can be determined by measuring their solubility in cadoxen in the
manner fully described in the copending application of DesMarais,
cited hereinabove.
High DS methyl cellulose soil release agents of the type employed
herein having the most preferred DP.sub.W range can be prepared
using cotton linters or wood-derived cellulose feedstock. It is
well known that cotton-based cellulose material has a DP.sub.W
greatly in excess of 1000. However, the caustic treatment during
methylation reduces the DP.sub.W due to the action of the caustic
on the cellulose polymers. Accordingly, cotton is a perfectly
acceptable source of cellulose when preparing the high DS materials
falling within the preferred DP.sub.W ranges cited herein.
Wood-derived cellulose is known to be comprised of cellulose
polymers having a DP.sub.W of about 2000, and below. Accordingly,
wood-based cellulose can easily be converted to the high DS methyl
materials having the preferred DP.sub.W range recited hereinabove
without the need for any additional degradation, since sufficient
degraduation will naturally occur on contact with the caustic used
in the methylation step.
The high DS methyl cellulose ethers employed in the instant
compositions are characterized by various parameters in the manner
described immediately below. Specific examples of optimal high DS
methyl cellulose soil release agents employed herein are set forth
in Table 1.
The DS (methyl) of the various cellulosic soil release agents
employed herein can be determined in the manner set forth in
"Methods in Carbohydrate Chemistry", III, Cellulose, R. L.
Whistler, Ed., Academic Press, New York, 1963, Section 49, by I.
Croon, at p. 277, et seq.
The gel point, or "cloud point", of the high DS methyl cellulose
ether soil release agents employed herein is determined in the
following manner. A 2% wt. aqueous solution of the cellulose ether
being tested is used to determine the gel point. Ten cc. of the 2%
solution are placed in a test tube and a thermometer is inserted
into the solution. The test tube containing the solution and
thermometer is immersed in a beaker of water on a hot plate. The
water is heated at a rate of approximately 1.degree.C/minute.
During this heating, the solution of cellulose ether is stirred
with the thermometer. The temperature is raised, slowly, until the
solution just becomes cloudy (the cellulose ethers exhibit a
negative temperature coefficient of solubility). The temperature at
which the solution clouds is the gel point of the cellulose ether
being tested.
The viscosity of the high DS methyl cellulose ethers is determined
on the basis of a 2% wt. aqueous solution in the manner disclosed
in ASTM Standard D-2363 for the determination of the apparent
viscosity of hydroxypropyl methyl cellulose. Following the ASTM
procedure, a 2% aqueous solution of the high DS methyl cellulose
ether is determined in an Ubbelohde tube viscometer. The 2%
solution is based on a dry mass of the product, i.e., the corrected
mass for moisture found in the sample.
The DP.sub.W of the high DS methyl cellulose ethers can be
experimentally determined in cadoxen, which is a standard solvent
for both substituted and unsubstituted cellulosics. In general
terms, the efflux time of a solution of a cellulosic derivative in
1:1 cadoxen: water is measured in a Cannon-Ubbelohde dilution
viscometer. The solution is diluted with additional solvent and the
efflux time is again measured. The dilution step is repeated twice
more, and the efflux times are again measured. The efflux time of
the solvent is also determined in the same viscometer. From these
data, the relative efflux time (or relative viscosity), the
specific viscosity, and then the reduced viscosity are calculated.
The reduced viscosity is plotted on linear graph paper vs.
concentration of cellulose derivative in g/dl. A line is drawn
through the points and extrapolated to zero concentration. The zero
concentration intercept is defined as the intrinsic viscosity. The
weight-average degree of polymerization, DP.sub.W, can then be
calculated by the Henley relationship as reported by W. J. Brown,
TAPPI, 49, 367 (1966). Complete details of the procedure are set
forth in the referenced application of DesMarais, above.
Typical examples of high DS methyl cellulose soil release agents of
the type employed herein are set forth in Table 1. It is to be
understood that these cellulosics are prepared by exhaustively
methylating cellulose in caustic in the manner well-known in the
art, and that this methylation procedure forms no part of the
present invention. The cellulosics having relatively low
viscosities (examples D and H) can be prepared by simply steeping
the cellulose in the caustic bath to degrade the anhydroglucose
"backbone" of the cellulose, in well-known fashion.
TABLE 1 ______________________________________ Cellulose DS
Viscosity Gel Pt. Ether (Methyl) DP.sub.W (cp) (.degree.C)
______________________________________ A 2.31 418 4,515 40 B 2.29
419 1,185 39 C 2.22 1,113 1,399 48 D 2.14 386 94 38 E 2.28 1,005
26,000 39 F 2.40 813 27,000 39 G 2.62 517 5,619 37 H 2.45 167 93 30
______________________________________
The following examples illustrate the fabric treating compositions
of the present invention, but are not intended to be limiting
thereof. As will be seen from the examples, the preferred
compositions herein comprise from about 3% to about 15% by weight
of a fabric softener/anti-static agent of the type disclosed
hereinabove and at least about 0.05%, preferably from about 0.05 to
about 10%, more preferably from about 0.25 to about 2.0%, by weight
of the methyl cellulose ether. Higher concentrations of the
components can be used, according to the desires of the
formulator.
The compositions herein can be formulated as solids or liquids.
When solid compositions are desired, a water-soluble, solid carrier
material is conveniently used in combination with the active
ingredients. Such carriers can be, for example, any of the
water-soluble organic or inorganic salts commonly used as
detergency builders, e.g., sodium citrate, sodium phosphate, sodium
carbonate, and the like. Exhaustive listings of such materials are
found in standard textbooks and in the patent literature; see, for
example, U.S. Pat. No. 3,526,592, the disclosures of which are
incorporated herein by reference. All such materials are compatible
in the present compositions and are safe for use in contact with
fabrics. Solid compositions are easily prepared by simply
dry-blending the active ingredients with the solid carrier.
Liquid compositions can be prepared by mixing the softener and soil
release cellulosic in a liquid carrier, e.g., water, mixtures of
lower alcohols such as ethanol or isopropanol and water, and the
like. When preparing liquid compositions, it is convenient to use
the lower viscosity methyl cellulosics to maintain pourability.
The compositions herein can contain minor amounts (e.g., 0.1 to 5%
by wt.) of additives such as perfumes, dyes, optical bleaches, and
the like to provide the corresponding aesthetic and performance
benefits.
EXAMPLE I
A liquid composition which softens and imparts a soil release
finish to fabrics is as follows:
Ingredient Weight % ______________________________________
Ditallowalkyldimethyl- ammonium chloride 7.5 Cellulose ether D* 1.5
Isopropyl alcohol 3.5 Perfume, dye and minors 1.0 Water Balance
______________________________________ *Cellulose ether D from
Table 1.
The composition of Example I is prepared by simply admixing the
ingredients in the proportions shown until a homogeneous mixture is
secured. The resulting composition has a viscosity ca. 150 cps, and
is easily poured.
A 5 lb. load of mixed polyester and polyester/cotton blend fabrics
is laundered with a commercial anionic detergent composition and
spray-rinsed. The fabrics are thereafter immersed in ca. 8 gallons
of fresh, 90.degree.F water in the deep rinse cycle of a standard
automatic washing machine. 2.0 Ounces of the composition of Example
I are poured into the water, which is agitated to evenly distribute
the composition. The fabrics are agitated gently for ca. 2 minutes,
after which the water is drained from the washer drum. The fabrics
are thereafter spun dry, and dried in a standard automatic clothes
dryer.
Fabrics treated in the foregoing manner are soft to the touch and
are substantially free from static cling.
Fabrics treated in the foregoing manner are spotted with dirty
motor oil, which is allowed to "set" under ambient conditions. The
fabrics are thereafter laundered in a commercial, fully built,
anionic detergent composition under standard household laundering
conditions, rinsed and dried. As a control, untreated fabrics and
fabrics treated with a low (ca 1.5-1.7 avg.) degree of methyl
substitution are similarly treated and laundered. The compositions
herein provide substantially superior release of the dirty motor
oil over untreated fabrics and fabrics treated using the low DS
methyl substituted soil release agents.
In the foregoing composition soil release ether D from Table 1 is
replaced by an equivalent amount of soil release ether H from Table
1 and equivalent results are secured.
In the foregoing composition, the ditallowalkyldimethylammonium
chloride is replaced by an equivalent amount of
ditallowalkyldimethylammonium bromide,
ditallowalkyldimethylammonium iodide, ditallowalkyldimethylammonium
fluoride, ditallowalkyldimethylammonium hydroxide, and
ditallowalkyldimethylammonium methylsulfate, respectively, and
equivalent results are secured.
In the foregoing composition the isopropyl alcohol is replaced by
an equivalent amount of methyl alcohol, ethyl alcohol, n-propyl
alcohol and n-butyl alcohol, respectively, and equivalent results
are secured.
EXAMPLE II
A solid composition which softens and provides a soil release
finish to fabrics is as follows:
Ingredient Weight % ______________________________________
Ditallowalkyldimethyl- ammonium chloride 7.5 Cellulose ether A* 1.5
Perfume, dye and minors 1.0 Sodium carbonate Balance
______________________________________ *Cellulose ether A from
Table 1.
The composition of Example II is prepared by simply blending the
ingredients in the proportions shown until a homogeneous mixture is
secured. The resulting composition is in powder form, and is easily
pourable.
Following the procedure set forth hereinabove for Example I, a 5
lb. load of mixed polyester and polyester/cotton blend fabrics are
laundered and spray-rinsed. The fabrics are thereafter immersed in
ca. 8 gallons of fresh, 90.degree.F water in the deep rinse cycle
of a standard automatic washing machine having 100 grams of the
composition of Example II dissolved therein. The fabrics are
agitated gently for ca. 5 minutes, after which the water is drained
from the washer drum. The fabrics are thereafter spun dry and dried
in a standard automatic clothes dryer.
The fabrics treated in the foregoing manner have a soft, desirable,
anti-static hand. The fabrics treated in a manner of Example II and
thereafter stained with hydrocarbon and vegetable oils exhibit a
substantial soil release effect when subsequently laundered with a
commercial, anionic detergent composition.
The composition of Example II is modified by replacing the
ditallowalkyldimethylammonium chloride with an equivalent amount of
dicoconutalkyldimethylammonium chloride,
dicoconutalkyldimethylammonium methylsulfate,
stearyldimethylammonium chloride, distearyldiethylammonium
chloride, ditallowalkyldipropylammonium bromide, and cetyl
pyridinium chloride, respectively, and equivalent results are
secured.
The composition of Example II is modified by replacing cellulose
ether A, from Table 1, with an equivalent amount of ethers B, C, D,
E, F, G and H, from Table 1, respectively, and equivalent results
are secured.
The foregoing compositions give good softening and superior soil
release performance on fabrics treated therewith. It will be
recognized that the compositions can readily be formulated to
contain various adjunct materials, in addition to the active and
the carrier. More particularly, various surfactants, used in
non-deterging amounts (i.e., 0.05 -1.0% wt.), can be employed in
the compositions to help disperse them throughout the rinse bath.
Nonionic surfactants, especially the ethoxylated alcohols and
ethoxylated phenols characterized by a hydrophilic lipophilic
balance (HLB) in the range from about 7 to about 15, and mixtures
of such materials, are preferred for this use. Exemplary nonionic
surfactants for this purpose include the tri-, penta-, hepta- and
nona-ethoxylated primary and secondary alcohols marketed under
various tradenames, e.g., Tergitol 15-S-7, Tergitol 15-S- 3,
Tergitol 15-S-9, and the Dobanols.
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