CA1137260A - Pretreatment composition for stain removal - Google Patents

Pretreatment composition for stain removal

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Publication number
CA1137260A
CA1137260A CA000354052A CA354052A CA1137260A CA 1137260 A CA1137260 A CA 1137260A CA 000354052 A CA000354052 A CA 000354052A CA 354052 A CA354052 A CA 354052A CA 1137260 A CA1137260 A CA 1137260A
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CA
Canada
Prior art keywords
ester
composition
active agent
carbon atoms
alcohol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000354052A
Other languages
French (fr)
Inventor
Ralph R. Sepulveda
Lynn H. Lander
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever PLC
Original Assignee
Unilever PLC
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Filing date
Publication date
Application filed by Unilever PLC filed Critical Unilever PLC
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Publication of CA1137260A publication Critical patent/CA1137260A/en
Expired legal-status Critical Current

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Abstract

ABSTRACT

A method and compositions for pre-laundering treat-ment of fabrics for stain removal are disclosed. The compo-sitions comprise 25-100% of an ester of a short chain alcohol and a fatty acid and 0-75% of a surfactant.

Description

' This invention applies to the field of composi-tions for the pretreatment of heavily soiled areas of tex-tiles prior to regular ~ashing. Many textile articles are not uniormly soiled; examples are tablecloths, pants' knees and collars and cufs on men's shirts. I a sultable pre-treatment is applied to the badly stained areas, better re-. .
sults can be obtained for the wash in general with less useof the detergent product. Especially difficult is finding a suitable pretreatment for the removal of greasy stains from fabrics such as polyesters.

Hydrophilic fibers, such as cotton, have a prefer-ential affinity for water over oil. During laundering, water displaces oily soil from the surface of the fabric, causing the soil to "roll-up"; the soil is then more readily removed by mechanical action. Polyester fibers, such as those made ~rom the copolymer of ethylene glycol and tereph'thalic acid, do not have this preferential affinity for water,'but rather, ' ~ are hydrophobic. Blends of polyester and cotton also ex-hibit hydrophobic tendencies. 'Due to this lack of affinity bet~een fiber and ~later, ordinary laundering o~ten does not satisfactorily remove oily soils from polyester-con~ainlng '' ~~
fibers. -.

,, ' ', '~ ', ' 1~3~
.. . . . . .
" ' -1 The use oE certain types of materials for pre-treàtment is known to the art. U.S. Patent 3,431,060 discloses a composition with a synthetic detergent and an optical brightener dispensed in aerosol form using a 5 suitable propellant. The active is broadly disclosed as being a nonionic, anionic or cationic surfactant.
U.S. Patent 3,417,023 discloses a pretreatment stick containing a gel-forming soap, a synthetic deter- !
gent and an optical brightener. The detergent is again broadly disclosedO
U.S. Patent 3,915,633 discloses a pre-wash com-posltion containing an organic complexing acid and a non-ionic or anionic surfactant. Among the sample nonionics mentioned are the esters polyglycerol monolaurate and gly-col dioleate. No example is given using either ester.
Certain organic es*ers are known to be cleaning aids. U.S. Patent 2,251,691 discloses partial esters of polyglycerol and fatty acids as being useful in dry clean-ing. U.S. Patent 2,251,694 discloses an ester of a hydroxy-carboxylic acid and a fatty acid as being useful in dry cleaning. The alkyl esters of fatty acids are disclosed by U.S~ Patent 1,875,530 as being useful ingredients of cosme--tics. Polyethylene glycol esters of fatty acids are dis- ¦
closed as having surfactant properties by U.S. Patent
2,528,13~.
U.S. Patent 2,462,758 discloses a detergent com-position consisting essentially of sulfate or sulfonated anionic surfactant and an monohydric ~lcohol or glycol ester. The ester is added to the composition in order to improve foaming characteristics.

1~L37~60 SUMMARY OF THE INVENTION
.. ,..................................... I

It is an object of the present invention to pro-vide a laundry pretreatment composition wllich will provide effective stain removal on polyester contain:ing fibers.
It is also an object of this invention to provide a laundry pretreatment composition which will effectively remove greasy-oily soils.
Still other objects and advantages of the present i~vention will become apparenk from the instant specifica-tion. --It has now been found that the above ohjects may be accomplished by the use of a pretreating composition comprising as an active system, about 25%~100% of an ester of a short chain alcohol and a fatty acid, about 0-75~ of l~ a nonionic surfactant and about 0-50% of an anionic surfac-. ... . .
tant. In a preferred embodiment the composition is non-aqueous and contains 50-90% ester and 10-50% of a surfac-tant.
:
DETAILED DESCRIPTION OF THE INVENTION

2~ The instant invention provides for a method of -treating stained fabric prior to laundering hy contacting said~ fabric with a composition which comprises about 25%
to about 100~ of an ester of a short chain alcohol and a fatty acid, 0 to about 75~ of a nonionic surfactant, and 2~ o to about 50~ of an anionic surfactant.
The esters encompassed by this invention are well known to the art. They are formed of alcohols con-taining 1 to about 4 carbon atoms and having one or more hydroxyl groups and fatty acids containing ahout 8 to about 22 ` ~37%6(~ 1 .
C~
carbon atoms, saturated or unsaturated, branched or straight chain. Fatty acid di-esters of t~le polyalkylene glycols, such as polyethylene glycol and polypropylene glycol, may also be used. These are nonionic in nature but have no surface active properties. Among the esters contemplated are:

S (1) Esters of monohydric alcohols of the formula R-OH, wherein R is an alkyl radical; such as isopropyl myristate, isopropyl palmitate, but~l stearate, butyl oleate, ethyl stearate!, isopropyl isostearate and methyl laurate (2) Glycerol esters such as glycerol monolaurate, glycerol mono- and di-oleate, and glycerol monostearake; also the corresponding esters of polyglycerol;
(3) Glycol esters such as ethylene glycol mono- ~' 15 ~ and di-stèaràte, diethylene glycol di-stearate, and mixtures thereof;
(4) Polyethylene glycol esters such as PEG di- ¦
- ~ stearate.
Mixtures of the above estexs may also be used, including esters produced by the reaction of alcohols with fatty acid groups, such as coconut oil or tallow fatty acids~
The amount and type of surfactant to be used in conjunction with the ester for maximum stain removal will 2~ depend on the type of stain and the type of fabric. In some applications, 100~ ester is desirable; in cthers a 50/50 mixture gives optimal results. Active compositions compris~
ing about 25~ to about 90~ ester, along with 0 to about 60 anionic surfactant and~0 to about 75~ nonionic surfactant ' .

37Z~O
.
are preferred for use where the range of fabrics treated will be broad, encompassing synthetics and synthetic/cot-ton blends.
The nonionic surface-active agents useful in this invention include those normally used in detergent compositions. Among these are:
(1) Polyoxyethylene condensates of alkyl phenols containing 6-12 carbon atoms in a straight or branched chain, and 2-25 E.O. units per molecule. Commercial surfactants of this 1-~!~ type are the Igepals and Tritons.
(2) Condensation products of aliphatic alcohols containing 8-22 carbon atoms in a straight or branched chain with ethylene oxide, 3-15 lS ~.O. units per molecule. Examples are the - ~ Tergitols and Neodols. -- (3) Condensation products of ethylene oxide with the reaction products of propylene oxide and diamine. Examples are the Tetronics.
20- (4) Condensation produc~s of ethylene oxide with the xeaction product of propylene oxide and propylene glycol. Examples are the Pluronics~
(5) Amine oxide surfactants having the formula RlR2R3 N ~ O wherein Rl and R2 are Cl-C3 alkyl groups and R3 is a C8-C22 alkyl with 0-2 hydroxyl groups.
(6) Phosphine oxide surfactants of the formula RlR2R3 P ~ O wherein Rl, R2 and R3 arP as defined above.

(7~ Sulfoxide surfactants of the formula .~ t~e l~rks --5~

37Z61~ 1 o R3~- S R2, whexein R3 and R2 a.re as de-fined above.
The anionic surface-active agents which may be used are those commonly found in detergent products. In-cluded are:
(1) The "soaps", alkali metal, ammonium and alkyl ammonium salts of C8-C22 fatty .¦
acids; ` .¦.
t2) alkali metal and ammonium salts of organic sulfuric reactions products containing an alkyl radical having 8 to 22 carbon atoms.
Examples are the alkyl sulfates, the alkyl ¦ :
sulfonates, and the alkyl benzene sulfon- 1, :
1~ ates; \
- - (3) the olefin sulfonates having 8-22 carbon -atoms;
: (4) the alkyl glyceryl ether sulfonates ha~ing 8-22 carbon atoms;
(5) alkali met.al salts of fatty acid monogly- -ceride sulfates and sulfonates; - .
(6) alkali metal salts of alkylphenol ethylene oxide ether sulfates, containing 1 12 E.O.
units per molecule and 8-22 carbon atoms ~ - in the`alkyl chain;
- (7) the.fa~ty acid isethionates;
(8) the alkyl ether sulfates having 1-30 E.O.
units per molecule and an alkyl or al.kenyl unit of 8-22 carbon atoms;
3~ (9) salts of.a fatty acid amide of a methyl tauride.

37~
.
Nonionic surfactants are preferred for the compo-sitions of this invention and may be used at levels up to about 75%~ Anionic surfactants are less effective in these compositions, but can still be used at levels up to about 60%.
In addition, the combinations of anionics and esters showed a tendency to separate in many cases, and were therefore less suitable for commercial application.
Mixtures of the various surfactants herein described may also be used. I
In addition to the surfactant/ester system, the pretreatment composition may contain other adjuvants known to the detergent art such as builders, bleaches, and opti- i cal brighteners. Other materials to ease dispensing may also be added. If the product is to be used in stick form, ~irming agents such as clays may be used; if it is to be dispensed as an aerosol, a propellant may be added.
In its most preferred form, the composition com-prises about 50-90% ester, 0 to about 50~ nonionic surface-active agent and 0 to about 50~ anionic surface-active agent, the total surfactant being a~out 10% to about 50~. The pre-ferred compositions contain little or no water, since added water can hasten hydrolysis of the ester, or separation of th~ surfactant and ester.
The preferred esters for use in the compositions are esters formed of alcohols of the formula R-OH wherein R is an alkyl radical, with fatty acids; isopropyl myristate and butyl stearate particularly preferred. The preferred sur-factants are nonionics with ethylene oxide condensates of primary and secondary alcohols having 11-15 carbon atoms 30- and 3-5 ~.O. units per molecule particularly preferred.

~3~;~6~

. . , The following examples serve to illustrate the invention. All proportions are by weight.
In the following e~amples, the procedure for determining stain removal is as follows:
, ~ 65/35 Dacron/cotton (D/C) and single knit poLy-ester swatches are s~ained with 3 and 5 drops of dirty mo~or oil, xespectively/ and the oil is allowed to be - absorbed into the,cloth for one hour. The result of the staining procedure is swatches with stains of approximately equal si~e. The reflectance of each swatch is then mea- ', sured with a Gardner Reflectance Spectrophotometer, Model No. XL-lO, CDM.' The stained swatches are treated by drop-ping a specified amount of a pretreatment composition on ', each stain, and adding two swatches to a pot containing l L5 , literof a standard detergent solution. The detergents, de-scribed belo~, and made up with 180 ppm (unless otherwise specified) hardness water (Ca~+:Mg+~ = 2:l~. The swatches are agitated in this detergent solution at 120F for 10 ' minutes, rinsed or one minute'in fresh 180 ppm, 120F 1 water, and dried in a commercial clothes dryer. A final reflectance value is then measured. Detergency is calcu-lated by subtracting the initial average reflectance of the soiled cloth before pretreatment from the reflectance of the cloth after'treating and drying. The ~ detergency 'is determined by dividing this detergency number by a num-ber representing the average difference in reflectance between a soiled cloth and a clean cloth. Thus, Ref (after washing) -_Re~ (after soiling) x lO0 , ~ detergency Ref ~-fore soiling) - Ref (after soillng) A difference in % detergency between two samples run together of about 5 percentage points should be considered a signifi-- 'cant difference~
- Two laundry detergents were used to wash the cloths.
Their compositions were as follows: ~
e m~rk ~ ~ -~L37260 J
- . Detergent A - _ -... , . - , -~lei~ht %
Sodium Linear Alkylbenzene Sulfonate (C14-C18 7.4 Sodium Plcohol Sulfate (Cl~-C18 chaln) 5.2 Sodium Fatty Alcohol E.O. Sulfate (C12-C1~ 4.2 chain, 4.7 E.O. Avera~e) Polyethylene Glycol (M.W. = 6000-7500) 1.6 Sodium Sulfate 36.6 Sodium Phosphates 23.2 Sodium Silicate (SiO2:Na2O = 2.4) . 10.4 Sodium Carbonate . 3.9 Water -- 6.8 Miscellaneous to 100 ' Detergent B
Weight oxylated Primary Alcohol - C14-ls Chain . Length,13 E.O. Average , . 8.9 , Sodium Soap . 1.0 : 20 Sodium Tripolyphosphate - 30,0 dium Silicate (SiO2:Na2O = 2.4) 4.5 Sodium Perborate 2.5 Sodium Sulfate 43.Q
Water 9 3 25 Miscellaneous to 100 - ~3~6~) 1 Test formulations were made up as follcws:
~ster - isopropyl myristate urEactant - C~ 5 secondary alcohol, 3 E.O. (sold by Union Carbide as Tergitol 15-S-3).

EsterNonionic Surfactant 1 - 100%
2 25% 75~ i 3 50% 50~ ,i ' 4 '75% 25%
100~
The detergent solution used in the testing was made from Detergent A. 0.5 grams pretreatment witli a~ove , mixture per swatch was used.
5 ~ .,. .. ~. Q Detergency ' Det. A conc. , Sample ~ /C Polyester .. - . ~ _ Control (no pretreatment) ' 2.0 16.2 4.2 1 - 1.4 28.9 2~.~
~0 2 ' - ' 1.4 35~8 39.2 3 1.4 39.2 40.8 4 ' 1.4 37.7 33.9 ' 1, ~ 40.8 21.6 I , The data show that it is more difficult to remove the stain from polyester than from blends with cotton,,prob-ably due to the aforementioned hydrophobic nature of poly-ester. On polyester, mixtures of nonionic and ester clearly ' show the greatest detergency. On Dacron~cotton, the ester alon~ is comparable to the mixtures.

~L~3726~) -... .~ .~ . , E~AMPLES 6-10 Test formulations were made up as follows:

Iso~ro~yl myristate Cll-15 sec- alcohol 5 E.O.
(Tergitol 15-S-5) 6 - 100%
7 25% 75%
8 50% 50%
9 75~ 25%
'100~ -The detergent solution was Detergent A. Pre-treat~ent = 0.5 g/swatch.

~ Deterqenc~
Det. A
Sample q/l D/C Polyester ~Control (no pretreatment) 2.0 28.4 , 1.5 6 1.4 20.3 13.8 7 1.4 37.3 32.3 - 8 - 1.4 55.4 46.1 - 9 1.~ 49.2 46.5 ~ 10 1.4 51.3 31.
, With this formulation peak detergency on poly-ester cloths appears to be somewhere in the range of 50-75~ ester; on Dacron/cotton comparable detergency was - found in the 50-100% ester range.

~11--~. ~
~3~

EX~MPLES 11-15 Test formulations:

Isopropyl m~ristate C11-15 sec- alcohol 7 E.O, (Tergitol 15-S-7) 11 - 100%
12 25% 75%
13 50% 50 14 75~ 25%
1~ 100%

Detergent solution: Detergent A. Pretrea-t-ment: 0.5 g/swatch.

~ Detergency Det. A
~ q~lD/C Pol!yester \
Control (no pretreatment) 2.0 28.5 3.4 ~`
' ~ .
11 1.4 15.9 8.1 12 1.~ 21.1 12.7 13 1.4 31.0 32.2 lg 1.4 36.8 33.1 2~ 15 1.4 49.4 43.0 This surfactant gives poorer detergency than - those with less E.O. per molecule. Improvements are ~ound with greater ester concentrations.

-12~

- ~37;~6C~ 1 The following formulations were made with primary alcohol ethoxylates and isopropyl m~ristate.

Isopropyl m~ristate Nonionic -- !
: 5 16 - 100% C12_15, 3 E-O-17 25~ 75~ C12-15' 3 E.O.
18 75% 25~o cl2-l5~ 3 E-O-19 100%
. 100% C12_1s~ 9 E-O- ;
21 25% -75% C12-15' 9 E.O. .
22 50% 50~ C12-15~
23 75~ 25% C12-15' 9 24 100~ - C12 15~ 9 E.O. .

The C12 15~ 3 E.O. surfactant is sold by Shell as Neodol .
C12 15, 9 E.O, surfactant is Neodol 25-9 ~
The detergent solution is Detergent A.

% Deter~enc~ _ Pretreatment Det. A . .
Sampleg/swatch ~ D/C Polyester 16 ~75 1~36 32~0 . 37~9 .
17 ~50 1~36 34~2 36~3 18 ~50 1~36 39~9 49~2 19 ~75 1.36 50~5 35.2 _ . . . _ .
Control (no pretreatment~ 2~0 22~8 3~4 - 20 ~50 1~4 10~1 16~7 21 50 104 18~2 14~2 22 ~ 50 1.4 32.4 42.2 23 .50 1.~ 48~9 S0~5 24 O50 1~4 46~1 37~

. ' I
--13-- !

~ ~372~
.. ` ` ` .~ .: . ` ~ . , .
The higher E.O. material again provides poorer detergency, with less ester. ~t higher ester concentra-tion, the differences between surfactants are small.

The following formulations were made with vari-ous esters as indicated, and Cll 15 secondary alcohol with : 5 EØ

ster Type Ester_% Nonionic Isopropyl myristate/ - 100% i palmitate blend 26 " 25% 75%
27 " 50% 50 - 28 " ; 75~ 25%
29 " . 100~ , -Butyl Stearate - 100~
31 . " 25~ 75% .
32 " 50% ~ 50%
33 " 75% 25 34 " 100~ -Detergent solution: Detergent A. Pretreatment:
0.5.g/swatch.

.

% Detergency Det. A
_g/l D/C Polyester Control (no pretreat- 2.0 29.9 4.5 ment) 1.~ 20.~ 17.3 26 . 1.4 30.8 33.5 27 1.4 60.2 52.0 28 1.4 53.4 55.9 29 1.4 49.3 40~5 Control (no pretreat- 2.0 31.0 4.9 ment) 1.4 19.9 16.4 31 1.4 34.5 29.0 32 1.~ S8.5 ~9.9 33 1.~ 41.9 36~3 34 1.4 ~6.0 22.1 1.
Both esters provide good results and,.for a variety of abrics are best used in proportions of 50-75% with 25-50~ noni.onic.

- Pretreatment was done using butyl stearate as ,' the ester and as surfactant, a condensate of ethylene -oxide with hydrophobic bases formed by condensing propy-lene oxide with pxopylene glycol, and having an aver.age molecular weight of about 2000 was used. This surfac-tant is known commercially as BASF-Wyandotte Pluronic L-61t and contains about 10~ ethylene oxide.

~ tra~ k - - 113 oJZ60 ~, ... . ~ . .
Sample EsterSurfactant - 100%
.` 36 25~ 75%
37 75~d 25%
. 38 100%

Detergent solution: Detergent A, 1.36 g/l.

. % Detergency Pretreatment Sample g/swatch D/C Polyester ~ 35 .75 12.1 1.8 . 36 .50 ~ 2~.0 18.3 37 .50 36.0 35~3 .
3~ .75 48.9 42.7 ` I
'`' . .
. EXAMPLES 39-42 \
,., , .., . _ ,, , Pretreatment wàs done with combinatio,ns of poly- ~
ethylene glycol (M.W. = 400) dioleate and dimethyl dihydro-gena~ed tallow amine oxide.

, Sam~le Ester Nonionic ~ ,_ 39 - 100%
.40 25% 75%
` 20 ~1 75% ` 25%
42 100% - .

oetergent solution: Detergent ~, 1.36 g/l.

-16~

~9~37~60 - - - . . ?
~ Deteraencv Pretreatment ~~
Sample g/swatch D/C Polyester 39 .75 13.3 6.5 .50 19.6 g.8 541 .50 35.3 31.1 42 .75 31.3 31.5 .
E~AMPL,ES 43-52 A series of dirty motor oil stains were pre- i treated with compositions consisting of 25% nonionic, 75%
isopropyl myristate, with washes in Detergent A, 120 ppm water. Pretreatment: 0.5 g~swatch. Results were as fol-.
lows:
.
~ Detergencv Det. A
lSSample Nonionic g/l D/CPolyester __ .
Control no pretreatment 2~033.0 2~3 43 Tergitol 15-S-3 1.4 53.646.3 44 Tergitol 15-S-5 1.4 57.852~8 Tergitol 15-S-7 1.4 40.631.1 20 46 Tergitol 15-S-9 1.4 43.848.4 47 ~eodol 25-9 1.4 46.748.0 Another series o dirty motor oil stalns were pretreated with compositions consisting of 75% nonionic and Z5% isopropyl myristate, with washes in Detergent A, 120 ppm water. Pretreatment: 0.5 g/swatch. Results are as follo~s:

-.

L3~
~ ~0 Dete~ency .
Sample Nonionic ~/1D/C Polyester Control no pretreatment 2.0 26.6 6.0 48 Tergitol 15-S-3 1.4 4~.2 46.0 49 Tergitol 15~S-5 1.4 35.1 36.3 Tergitol 15-S-7 1.4 20.6 15.3 Sl Tergitol 15-S-9 1.4 22.1 15.2 52 Neodol 25-9 1.4 25.7 21.1 With compositions high in nonionic, peak stain removal is obtained with Tergitol 15-S-3, with 15-S-5 also acceptable. With the low-nonionic compositions, Tergi-tol 15-S-5 is the best performer, although the others were ~3 acceptable. Overall stain removal is better with the low-nonionic composition.
, - \ I

, Test formulations were made up as follows:
.
Isopropyl -Sam~le Myristate Anionic - 53 25% 75% sodium C14-C16 alpha olefin sulfonate 54 75% 25% sodium secondary alkane sulfonate 25~ 75% sodium secondary alkane sulfonate 56 75~ 25% sodium lauryl hydroxy ether sulfonate 57 75% 25~ sodium C10 linear alcohol sulfate , Det~rgent solution: Detergent B, 1.99 g/l.
2~ Pretreatment = 0.5 g/swatch.

.
, 1137261~ ~
., ., ~ . . . .
.
% Detergency Sample D/CPolyester Control (no pretreatment) 35.3 7.4 53 27,69~9 54 50.630.7 29.38.7 56 51.427.4 57 53.026.6 Sample 55 was a translucent-opaque gel-like vis-
- 10 cous paste. ~11 other samples showed some separation, but were readily dispersed upon shaking.
~.- ., , . , Test formulations were made up as follows: ) Isopro ~ Myrlstate Surfactant 58 ~ 50% 50% Na C10 Alcohol Sulfate 59 25% 50% Na C10 Linear Alcohol Sulfate 3 - 25% Cll-cl5 Sec AlcO
5 E.O.

20Detergent solution: Detergent B, 1.99 g/l.
Pretreatment: 0.5 g/swatch.

% Detergency D/C Polyester Control lno pretreatment) 36.4 2.6 S8 - 51.6 24.5 ~9 42.2 23.2 Compositions containing 75% anionic and 25~ ester were generally ineffective. Compositions with 50% anionic were accepta~le.

Claims (16)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROEPRTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An active composition for the pre-laundering treatment of stains on fabrics consisting essentially of (a) about 25% to about 90% of at least one ester formed of a fatty acid of about eight to about twenty-two carbon atoms chain length, and (1) an alcohol of one to about four carbon atoms chain length; or (2) a polyalkylene glycol which is a poly-ethylene or polypropylene glycol; and wherein said ester is a di-ester;
(b) 0 to about 75% of at least one nonionic sur-face-active agent;
(c) 0 to about 60% of at least one anionic sur-face-active agent;

the total of (b) and (c) being about 10% to about 75%.
2. The composition of claim 1 wherein said ester is formed of said fatty acid and an alcohol of the formula R-OH wherein R is an alkyl radical of one to about four carbon atoms chain length.
3. The composition of claim 1 wherein said ester is a di-ester formed of polyethylene glycol and a fatty acid.
4. The composition of claim 1 comprising about 25% to about 90% of said ester and about 10% to about 75%
of said nonionic surface-active agent.
5. The composition of claim 1 comprising:
(a) about 50% to about 90% of said ester;
(b) 0 to about 50% of said nonionic surface-active agent; and (c) 0 to about 50% of said anionic surface-active agent;
the total of (b) and (c) being about 10% to about 50%.
6. The composition of claim 2 wherein said ester is isopropyl myristate.
7. The composition of claim 2 wherein said ester is butyl stearate.
8. The composition of claim 3 wherein said ester is polyethylene glycol dioleate, wherein the polyethylene moiety has a molecular weight of about 400.
9. The composition of claim 4 wherein said ester is isopropyl myristate and said nonionic surfactant is a C11-C15 secondary alcohol with 3-5 ethylene oxide units per molecule.
10. The composition of claim 5 wherein said non-ionic surface-active agent is present at a level of about 10% to about 50%.
11. The composition of claim 5 wherein said ester is isopropyl myristate present at a level of about 50% and said nonionic surface-active agent is a C11-C15 secondary alcohol with about 3-5 ethylene oxide units per molecule present at a level of about 50%.
12. The composition of claim 5 wherein said ester is iso-propyl myristate present at a level of about 25%, said non-ionic surface-active agent is a C11-C15 secondary alcohol with about 5 ethylene oxide units per molecule present at a level of about 25%, and said anionic surface-active agent is sodium C10 linear alcohol sulfate present at a level of about 50%.
13. A method for the pre-laundering treatment of stained fabrics comprising contacting said stained fabric with an active composition comprising:
(a) about 25% to about 90% of at least one ester formed of a fatty acid of about eight to about twenty-two carbon atoms chain length, and (1) an alcohol of one to about four carbon atoms chain length or (2) a polyalkylene glycol which is a poly-ethylene or polypropylene glycol; and wherein said ester is a di-ester;
(b) 0 to about 75% of at least one nonionic sur-face-active agent; and (e) 0 to about 60% of at least one anionic sur-face-active agent.
14. A method for the pre-laundering treatment of stained fabrics comprising contacting said fabrics with an active composition comprising at least one ester formed of a fatty acid of about 8 to 22 carbon atoms chain length, and (i) an alcohol of one to about four carbon atoms chain length or (ii) a polyalkylene glycol which is a polyethylene or polypropylene glycol and wherein said ester is a diester.
15. The method of claim 14 wherein said ester is an ester of a fatty acid and an alcohol of the formula R-OH wherein R is an alkyl radical of one to about four carbon atoms chain length.
16. The method of claim 15 wherein said ester is isopropyl myristate or butyl stearate.
CA000354052A 1979-06-18 1980-06-16 Pretreatment composition for stain removal Expired CA1137260A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US4977479A 1979-06-18 1979-06-18
US049,774 1979-06-18

Publications (1)

Publication Number Publication Date
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Family

ID=21961660

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5298195A (en) * 1992-03-09 1994-03-29 Amway Corporation Liquid dishwashing detergent

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5298195A (en) * 1992-03-09 1994-03-29 Amway Corporation Liquid dishwashing detergent
US5443757A (en) * 1992-03-09 1995-08-22 Amway Corporation Liquid dishwashing detergent

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