AU4270789A - Detergent composition - Google Patents

Detergent composition

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Publication number
AU4270789A
AU4270789A AU42707/89A AU4270789A AU4270789A AU 4270789 A AU4270789 A AU 4270789A AU 42707/89 A AU42707/89 A AU 42707/89A AU 4270789 A AU4270789 A AU 4270789A AU 4270789 A AU4270789 A AU 4270789A
Authority
AU
Australia
Prior art keywords
carbon atoms
composition according
sulphosuccinate
alkyl groups
composition
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.)
Granted
Application number
AU42707/89A
Other versions
AU622932B2 (en
Inventor
Mohamad Sami Falou
Reginald Vear Scowen
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
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Unilever PLC filed Critical Unilever PLC
Publication of AU4270789A publication Critical patent/AU4270789A/en
Application granted granted Critical
Publication of AU622932B2 publication Critical patent/AU622932B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/83—Mixtures of non-ionic with anionic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Description

M32,
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L MICOCP RESOLUTION TEST CHART NA4oABUREAU OF sTANIJARDS STANDAI~D REFERENCE MATERIAL loioa (ANSI arndISO TEST CHART No. 2)
N Ar, n7 /I
'2 FORM 1
COMMONWEALTH OF AUSTRALIA
PATENTS ACT 1952
APPLICATION FOR A STANDARD PATENT
I\We, UNILEVER PLC of UNILEVER HOUSE BLACKFRIARS LONDON EC4 ENGLAND hereby apply for the grant of a standard patent for an invention entitled:
c~ DETERGENT COMPOSITION. c I Irr Ctsr which is described in the accompanying complete specification Details of basic application(s):
Number of basic Name of Convention country in Date of basic application which basic application was application filed 8824599.8 20 OCT 88
My/our address for service is care of GRIFFITH HACK CO., Patent Attorneys, 601 St. Kilda Road, Melbourne 3004, Victoria, Australia. t r
t f DATED this 10th day of October 1989
UNILEVER PLC GRIFFITH HACK CO.
'7(f
TO: The Commissioner of Patents.
Australia Patent Declaration Form
Forms 7 and 8
AUSTRALIA
Patents Act 1952
DECLARATION IN SUPPORT OF A CONVENTION OR NON-CONVENTION APPLICATION FOR A PATENT OR PATENT OF ADDITION no. 42707/89 Name(s) of In support of the application/made by UNILEVER PLC Applicant(s)
Title for a patent for an invention entitled DETERGENT COMPOSITION
Name(s) and I!MU DILSHAD RAJAN, of address(es) Unilever House, Blackfriars, London EC4P 4BO. England of person(s) making declaration do solemnly and sincerely declare as follows:-
1. amec>daet<he<Qpp6oi xtox?3^ tau x authorised by the abovementioned applicant to make this declaration on its behalf.
2. The basic application(s) as defined by Section 141 of the Act was/wmm made in the following country or countries on the following date ak by the following applicant(s) namely:- Country,filing Great Bri-nin on 20 October 1988 date and name bv Unilever ol of Applicant(s) by Unilever Dlc for the or on each basic by application
3. The said basic application(s) was/were the first application(s) made in a Convention country in respect of the invention the subject of the applica-ion. Name(s) and 4. The actual inventor(s) of the said invention AS/are address(es) Mohamad Sami FALOU of 8 Hill Close, Oldham, Lanes OL4 of the or England; and Reginald Vear SCOWEN of 113 Brookhurst Road, each actual Bromborough, Wirral, Merseyside L63 OEH, England 'inventor See reverse 5. The facts upon which the applicant(s) is/are entitled side of this to make this application are as follows:- form for The said applicant is the assignee of the said actual guidance in inventors. completing this part
DECLARED at London, Englandthis day of October 1989
1)1s o0 cC a A a i L i aP, a a a C Ci C tl~
(12) PATENT ABSTRACT (11) Document No. AU-A-42707/89 (19) AUSTRALIAN PATENT OFFICE
(54) Title DETERGENT COMPOSITION
International Patent Classification(s) (51)4 C1D 001/83 C11D 001/25 C11D 001/72 (21) Application No. 42707/89 (22) Application Date 10.10.89 Priority Data (31) Number (32) Date (33) Coi untry 8824599 20.10.88 GB UNITED KINGDOM (43) Publication Date 26.04.90 (71) Applicant(s) UNILEVER PLC (72) Inventor(s) NAME NOT GIVEN (74) Attorney or Agent GRIFFITH HACK CO. MELBOURNE (57) Claim 1. A detergent compo sition comprising:
1 to 50% by weight of a surfactant system which is a mixture
of:
i) dialkylsulphosuccinate, the alkyl substituent groups of
which contain at least 4 carbon atoms each and contain 12 to
carbon atoms in total; and
ii) an alkoxylated nonionic surfactant which has an HLB
value not above 10.5;
the ratio of i) to ii) lying between 7:1 and 1:7, and
to 60% by weight of detergency builder.
-I
(11)42707/89 -2-
12. A method of washing which comprises contacting
soiled material with a built aqueous wash liquor which is a
solution of surfactant system comprising a mixture of:
i) dialkylsulphosuccinate, the alkyl substituent groups of
which contain at least 4 carbon atoms each and contain 12 to
carbon atoms in total; and
ii) an alkoxylated nonionic surfactant which has an HLB
value not above 10.5;
the ratio of i) to ii) lying between 7:1 and 1:7.
IL
AUSTRALIA PATENTS ACT 1952 Form COMPLETE SPECIFICATION
(ORIGINAL) FOR OFFICE USE
Short Title:
Int. Cl:
Application Number: Lodged:
Complete Specification-Lodged: Accepted: S Lapsed: Published: 0' n. Priority:
Related Art: 4 t
TO BE COMPLETED BY APPLICANT
Name of Applicant: UNILEVER PLC r Address of Applicant: UNILEVER HOUSE 9 BLACKFRIARS LONDON EC4 ENGLAND
Actual Inventor:
Address for Service: GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.
Complete Specification for the invention entitled: DETERGENT COMPOSITION.
The following statement is a full description of this invention including the best method of performing it known to me:-
1A
DETERGENT COMPOSITION
This invention relates to a detergent composition
for cleaning soiled materials using a built aqueous wash
liquor, and in particular but not exclusively to a detergent
composition for washing fabrics.
Fabric washing compositions contain, as an
essential ingredient, a detergent active system whose role
is to assist in the removal of soil from fabric and its
10 suspension in the wash liquor. Suitable detergent active materials fall into a number of classes, including anionic,
nonionic and cationic materials and marketed products e. contain materials selected from one or more of these
classes.
A known group of compounds which fall into the
class of anionic detergent active materials are the *Se
a dialkylsulphosuccinates. These materials have been used as t 1 detergent active materials in products for other cleaning
purposes, such as in dishwashing compositions. However, dialkyvlsulphosuccinates have not found favour in detergent
compositions intended to give a built wash liquor, such as
compositions intended for washing fabrics. We have now discovered that enhanced performance
from dialkylsulphosuccinates in solution in a built wash
liquor can be achieved by specific selection of alkyl
substituent groups and by mixing with a specific nonionic
detergent active material. Thus, according to the
invention there is provided a detergent cbmposition
1 i r. 2 comprising:
1 to 50% by weight of a surfactant system which is a mixture
of:
i) a dialkylsulphosuccinate, the alkyl substituent groups
of which contain at least 4 carbon atoms each and contain 12
to 20 carbon atoms in total; and
S 10 ii) an alkoxylated nonionic surfactant which has an HLB
value not above 10.5, preferably below this as indicated
below, 0 4
0 44
the ratio of i) to ii) lying between 7:1 and 1:7; and
to 60% by weight of detergency builder.
SThe balance of any detergent composition may be
selected from water and other ingredients conventionally
encountered in detergent compositions. According to a second aspect of this invention
there is provided a method of washing which comprises Scontacting soiled material with a built aqueous wash liquor
which is a solution of surfactant system comprising a
mixture of:
i) dialkylsulphosuccinate, the alkyl substituent groups of
which contain at least 4 carbon atoms each and contain 12 to
S-
3
carbon atoms in total; and
ii) an alkoxylated nonionic surfactant which has an HLB
value not above 10.5;
the ratio of i) to ii) lying between 7:1 and 1:7.
For a given total number of carbon atoms in the
two alkyl groups of the sulphosuccinate, it is advantageous
0 040 10 that the alkyl groups contain the same number of carbon atoms so that the dialkylsulphosuccinate is symmetrical. It I tt is then possible for other dialkylsulphosuccinate molecules, with alkyl substituents of different chain length or with rfit
t" unsymmetrical substituents, to be present also. It is preferred however, that of all dialkylsulphosuccinate
molecules present in the composition at least 55% of the alkyl chains, preferably at least 70% of the alkyl chains
are of the same length.
We have found that the optimum chain length for
the alkyl substituents is seven carbon atoms, especially
when these C7 alkyl groups are of straight chain formation.
Suitable nonionic surfactants which may be used
C are alkoxylated materials which are the reaction products of
Scompounds having a hydrophobic group and a reactive hydrogen
atom, for example aliphatic alcohols, acids, amides or alkyl
phenols with alkylene oxides, especially ethylene oxide
either alone or with propylene oxide. Specific alkoxylated nonionic detergent compounds are alkyl (C6 -C2 2 phenols-
-r w~
ethylene oxide condensates, the condensation products of
aliphatic (C8 -Cg primary or secondary linear or branched
alcohols with ethylene oxide, and products made by
condensation of ethylene oxide with the reaction products of
propylene oxide and ethylenediamine.
Alkylene oxide adducts of fatty materials are
preferably used as the nonionic surfactants. The number of
alkylene oxide groups per molecule has a considerable effect
upon the HLB of the nonionic surfactant. The chain length
10 and nature of the fatty material is also influential, and thus the preferred number of alkylene oxide groups per
molecule depends upon the nature and chain length of the a 4 fatty material. 44&$
As indicated above, the nonionic surfactant has an
HLB value not above 10.5. It is preferred that the nonionic
surfactant has an HLB value below 10, preferably below 9.
The surfactant system may include other surfactant
materials in addition to the specified
dialkylsulphosuccinate and nonionic materials. These other
surfactant materials may be selected from anionic detergent
active materials, zwitterionic or amphoteric detergent
active materials or mixtures thereof.
Preferably, any such further surfactant materials
are present at a level which is no more than a minor amount
of the total amount of surfactant in the composition.
For compositions in which the
dialkylsulphosuccinate has alkyl groups with a total of 14
carbon atoms or less, it is possible to have electrolyte
I
present in the wash liquor, without detriment to detergency.
There may well be enough electrolyte to give a concentration
of at least 0.05 molar, preferably at least 0.1 molar when
the composition is used at a concentration of 1 g/14 tre.
If more than half of the sulphosuccinate has alkyl
groups with a total of 16 carbon atoms, or more, it is very
desirable to restrict the concentration of electrolyte in
the wash liquor to not over 0.05 molar, preferably 0.035
molar. (The concentration of surfactant in the wash liquor
is likely to be from 0.05 to 2.0 g/litre, preferably 0.1 to
o* 9 0 1.0 g/litre.
More specifically, if more than half of the
a 'o@o sulphosuccinate has alkyl groups with a total of 16 or more o"o carbon atoms, it is desirable that the ionic strength of the
15 wash liquor should not exceed 0.05 moles/litre preferably 0.035 moles/litre.
Ionic strength is related to concentration but
takes account of the numbers of ions in a molecule and multiple charged ions.
20 Ionic strength is calculated from the molarity (m)
of each ionic species present in solution and the charge (z)
carried by each ionic species. Ionic strength is one
half the summation of m.z 2 for all ionic species present
i.e.
I S m.z2 E
For a salt whose ions are both univalent, ionic
strength is the same as the molar concentration. This is
not so where more than two ions or multiple charges are r involved. For instance a 1 molar solution of sodium carbonate contains 2 moles/litre of sodium ions and 1 mole/litre of carbonate ions carrying a double charge.
Ionic strength is given by:
I [2(12) 1 x 3 moles/litre
A description of ionic strength is given in
"Physical Chemistry" by Walter J. Moore, 4th Ed. 1963.
The level of electrolyte in the wash liquor is
not, in practice, a parameter over which the domestic user
of a fabric washing product exercises direct control. It
on is determined, inter alia by the level of water-soluble
salts present in the product and the recommended dosage for o000
0 0'o 90 that product. Thus forms of the present invention using o o alkyl groups with a total of 16 or more carbon atoms are of
15 particular value in two circumstances, i.e. i) where recommended dosage levels are low, as for example in North
America, and ii) where the product contains high levels of S water-insoluble material, as for example where the product
contains a water-insoluble detergency builder material. The
20 only water-insoluble detergency builder material which has
ibeen used extensively is zeolite, a crystalline
aluminosilicate ion-exchange material, but the invention
would also be of value to products containing any other
water-insoluble builder material. Detergent compositions
are generally used in amounts greater than 1 gram/litre,
usually in the range from 4 g/litre to 10 g/litre.
The detergent composition of this invention may
comprise from 1% to 50% by weight of the surfactant system.
6Lb- -A e i I
Preferred is that the amount of the surfactant system should
range from 2% better 4 or even 6% by weight up to 30 or
Any electrolyte which is present will generally be
a water-soluble salt. This may be such a salt as will
provide a benefit in terms of the fabric washing process
such as a water-soluble detergency builder salt or a water-
soluble alkaline salt. Alternatively the electrolyte may be
constituted by a water-soluble filler salt such as sodium
sulphate or sodium chloride. Salts from all three classes
may be present.
o Generally, compositions according to the invention ao will contain some electrolyte, for example ranging frc;i
go up to 90% by weight of the composition, so as to give an ionic strength of at least 5 x 10 3 moles/litre, more likely 09 15 at least 0.01 moles/litre in a wash liquor. A wash liquor
may have an electrolyte concentration of at least 0.01
molar.
S When a low level of electrolyte is required the Scomposition may comprise not more than 60% by weight,
S 20 preferably not more than 40% by weight of water-soluble r alkali metal salts, and may also contain from 10% to 60% by
weight, preferably from 20% to 50% by weight, of a water-
insoluble detergency builder material. a 9
It is desirable that the compositions according to
the invention be approximately neutral or preferably
alkaline, that is when the composition is dissolved in an
amount to give surfactant concentration of 1 g/1 in
distilled water at 25 0 C the pH should desirably be at least
I _Er-
ILr---r_
8
6, preferably at least 8 and yet more preferably at least To this end the compositions may include a water-
soluble alkaline salt. This salt may be a detergency
builder (as described in more detail below) or a non-
building alkaline material.
The amount of detergency builder can range from
to 60% by weight. It may be preferred to use from at least
by weight to 50% by weight. The detergency builder may
be any material capable of reducing the level of free
0 calcium ions in the wash liquor and will preferably provide
the compositions with other beneficial properties such as Sthe generation of an alkaline pH and the suspension of soil o
removed from the fabric.
Examples of phosphorus-containing inorganic
detergency builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates,
orthophosphates, polyphosphates and phosphonates. Specific
°t examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates and
20 hexametaphosphates.
Examples of non-phosphorus-containing inorganic
detergency builders, when present, include water-soluble
Salkali metal carbonates, bicarbonatos, silicates and
crystalline and amorphous aluminosilicates. Specific
examples include sodium carbonate (with or without calcite
seeds), potassium carbonate (with or without calcite seeds),
sodium and potassium bicarbonates and silicates.
Examples of organic detergency builders, when present, include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxsulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid.
Apart from the ingredients already mentioned, a
number of optional ingredients may also be present.
o 10 Examples of other ingredients which may be present in the
o composition are polymers containing carboxylic or sulphonic acid groups in acid form or wholly or partially neutralised *o*o to sodium or potassium salts, the sodium salts being
preferred. Preferred polymers are homopolymers and
15 copolymers of acrylic acid and/or maleic acid or maleic t
o anhydride. Of especial interest are polyacrylates,
acrylic/maleic acid copolymers, and acrylic phosphinates. Suitable polymers, which may be used alone or in
combination, include the following:
S 20 polyacrylic acids, for example Versicol (Trade
Mark) E5, E7 and E9 ex Allied Colloids, Narlex (Trade Mark)
LD 30 and LD 34 ex National Adhesives and Resins Ltd,
Acrysol (Trade Mark) LMW-10, LMW-20, LMW-45 and Al-N ex Rbhm
Haas, and Sokalan (Trade Mark) PA-20, PA-40, PA-70 and PA-
110 ex BASF;
ethylene/maleic acid copolymers, for example the
EMA (Trade Mark) series ex Monsanto;
methyl vinyl ether/maleic acid copolymers, for example, Gantrez (Trade Mark) AN 119 and AN 149 ex GAF
Corporation;
acrylic acid/maleic acid copolyme's, for example,
Sokalan (Trade Mark) CP4, CP5 and CP7 ex BASF, and the
Alcosperse (Trade Mark) series ex Alco;
acrylic phosphinates, for example, DKW (Trade
Mark) 125 ex National Adhesives and Resins Ltd, and the
Belsperse (Trade Mark) series ex Ciba-Geigy. cc The molecular weights of homopolymers and
S 10 copolymers are generally 1000 to 150,000, preferably 1500 to
"ao 100,000. The amount of any polymer may lie in the range
from 0.5 to 5% by weight of the composition. Other suitable
o polymeric materials are cellulose ethers such as carboxy methyl cellulose, methyl cellulose, hydroxy alkyl
celluloses, and mixed ethers, such as methyl hydroxy ethyl
S* cellulose, methyl hydroxy propyl cellulose, and methyl
S' carboxy methyl cellulose. Mixtures of different cellulose
ethers, particularly mixtures of carboxy methyl cellulose
and methyl cellulose, are suitable. Polyethylene glycol of
S 20 molecular weight from 400 to 50,000, preferably from 1000 to
10,000, and copolymers of polyethylene oxide with polypropylene oxide are suitable as also are copolymers of
polyacrylate with polyethylene glycol. Polyvinyl
pyrrolidone of molecular weight of 10,000 to 60,000
preferably of 30,000 to 50,000 and copolymers of polyvinyl
pyrrolidone with other poly pyrrolidones are suitable.
Polyacrylic phosphonates and related copolymers of molecular
weight 1000 to 100,000, in particular 3000 to 30,000 are r. 11 also suitable.
Further examples of other ingredients which may be
present in the composition include fabric softening agents
such as fatty amines, fabric softening clay materials,
lather boosters such as alkanolamides, particularly the
monoethanolamides derived from palm kernel fatty acids and
coconut fatty acids, lather depressants, oxygen-releasing
bleaching agents such as sodium perborate and sodium
percarbonate, peracid bleach precursors, chlorine-releasing 04 0 0 10 bleaching agents such as trichloroisocyanuric acid, O inorganic salts such as sodium sulphate, and, usually o 0 4tt present in very minor amounts, fluorescent agents, perfumes
including deodorant perfumes, enzymes such as cellulases, Oitt
proteases and amylases, germicides and colourants.
The detergent compositions according to the invention may be in any suitable form including powders,
bars, liquids and pastes. For example suitable liquid compositions may be non-aqueous or aqueous, the latter being
either isotropic or lamellar structured. The compositions
may be prepared by a number of different methods according
to their physical form. In the case of granular products
they may be prepared by dry-mixing or coagglomeration.
SDialkylsulphosuccinate is preferably not subjected to
conventional spray-drying, because it is hydrolytically
unstable. The specified nonionic surfactants can be
liquified by melting or solvent dissolution and sprayed onto
preformed base powder granules.
An example of a granulaz; detergent composition which can be used at a dosage of 6 g/litre to yield an ionic strength of 0.023 mole/litre is: by weight
Dialkylsulphosuccinate
Nonionic surfactant 6
Zeolite
Alkaline silicate 3
Polyacrylate 4 Sodium carbonate 6
Sodium sulphate
Water and minor constituess which are not electrolytes balance to 100%
The invention will now be described in more detail
in the following non-limiting examples.
EXAMPLES
S'o. A number of examples and comparative examples were
i 20 carried out. These examples compared the soil removal
(specifically triolein removal) from fabrics using various compositions.
The experimental conditions were the same in each
case. Wash liquors were used to wash a fabric load in a
Tergotometer at a liquor to cloth ratio of 40:1. Washing
was carried out at 40°C for 20 minutes, with agitation at
The load consisted of a number of polyester test
cloths to which had previously been applied an amount of C 1 4
labelled triolein. Measurement of the level of labelled
-i
triolein after washing, using radiotracer techniques gave an
indication of the degree of detergency (soil removal).
Various dialkylsulphosuccinate compounds were
used. All had straight alkyl chains. The material
indicated below as C 6 /C8 was a mixture consisting of
molecules with one C 6 and one C 8 alkyl group, molecules with
two C6 alkyl groups and molecules with two C7 alkyl groups,
in a 2:1:1 ratio.
Nonionic surfactants were C 1 2 alcohol ethoxylated
I' 10 with differing average amounts of ethylene oxide, as stated
below. 04
q In a first series of experiments, for each tested Q
composition, wajh liquors were made up containing 1 g/l of
the surfactant mixture and 0.1 molar sodium chloride (to
represent the electrolyte level which would derive from
other components of the composition in practice) at a pH of For sodium chloride electrolyte concentration and ionic strength are the same. SIn a second series of experiments wash liquors 4tI
again contained 1 g/l uf th. surfactant mixture and had an
S, ionic strength of 0.1 mole/litre but the electrolyte was T 1.8 g/l sodium tripolyphosphate, 0.48 g/l sodium silicate
and 3.9 g/1 sodium chloride, giving a pH of
Results of both series of experiments are given in
Table 1 below.
TABLE 1
Example No 1 2 3 4
pH 6.5 10 6.5
Alkyl groups on diC7 diC7 C C diC 8 sulphosuccinate straight straight straight straight Ethylene oxide 3 3 3 3 residues on C 1 2 alcohol Sulphosuccinate: Nonionic ratio %triolein removal 000
9000 100:0 18.2 62.0 11.0 28.8 *0 15 87.5:12.5 11.9 28.8 00 0.
0 75:25 27.4 69 .9 13.1 25 .9
o0.00 62. 5: 37. 5 18.6 71.3 6.9 21.7
50:50 6.7 68.8 5.9 12.
37. 5: 62. 5 39.0
25:75 4.3 4.8
0:100 0.5
09 0 A further series of experiments was carried out at A44
a lower ionic strength of 0.02 mole/litre. Results are set
out in Table 2 below.
F
7
TABLE 2
Example No 5 6 7 8 9
pH 6.5 6.5 10 10
Alkyl groups C6 /C 8 C6 C6 C,/C 8 diC, on sulpho- straight straight straight straight straight succinate
Ethylene oxide 3 residues on C1 2 alcohol o s Sulphosuccinate: 0404 4 15 Nonionic ratio triolein removal "4 100:0 6.8 6.8 11.0 11.0 31.9 o *O
4.: 80:20 7.3 4.8 21.3 10.1 34.4 1I
4440 60:40 10.1 4.5 38.3 14.9 42.4
50:50 8.7
40:60 5.3 8.5 44.8 27.5 35.4
20:80 4.6 30.6 15.8 53.13 17.6 0:100 59.9 77.5
Comparison of Examples 5 and 6 and comparison of
Examples 7 and 8, all in Table 2, shows that greater
detergency occurs with a mixture of the low HLB nonionic and
dialkylsulphosuccinate than with either of these components
alone. This synergistic effect is not observed with the
higher HLB nonionic. The same synergistic effect is observed with Examples 1 to 3 in Table 1.
It can be seen from the Examples that the
synergistic effect is obtained both at approximately neutral
pH and at alkaline pH, and under both low electrolyte (0.02
7. 16
mole/litre) and higher electrolyte (0.1 mole/litre)
conditions, except however in the case of diC8
alkylsulphosuccinate for which synergy is observed at low
electrolyte only (Example 9). It can be seen also that synergy generally occurs
at sulphosuccinate:nonionic ratios between 1:4 and 4:1, and
that diC alkyl sulphosuccinate gives best performance. Further examples demonstrate liquid compositions
built with sodium citrate, as set out in Table 3 below. The
compositions were added to water in an amount of 12 g/l, to
provide wash liquors containing 1.7 g/l surfactant, an 2 electrolyte concentration of 1.18 x 10- molar and anionic
strength of 3.42 x 10- 2 moles/litre. The removal of
labelled triolein was measured as set out above and the
result is included in Table 3. The sulphosuccinate used had
C, straight alkyl groups. the nonionic surfactant was C12 alcohol ethoxylated with an average of 3 ethylene oxide
residues.
4 i
4 1 *t
L- 4 i
17
TABLE 3
Example No 11
Constituent by weight DiC 7 alkyl- sulphosuccinate 13
C1 2 3EO 6.5 13 .0 Glycerol 4 4 4 Borax 1.3 1.3 1.3 Sodium citrate 10 10 o to Sodium chloride 3 3 3 or
It Ethanol 30 30 it 0 Water balance to
Triolein removal was
Example 10 sulphosuccinate only 11.0 Example 11 sulphosuccinate nonionic 71.2 Example 12 nonionic only 1.1
i Similar examples were carried out using slightly
different liquid formations as detailed in Table 4 below,
using 6 g/l to make up wash liquors containing 0.85 g/l
surfactant, with an electrolyte concentration of 6.26 x 10-3
mole/litre and an ionic strength of 1.16 x 10- 2 mole/litre.
I
18
TABLE 4
Example No 13 14
Constituent by weight
DiC, alkyl- sulphosuccinate 13
C 2 3EO 6.5 13
Glycerol 1.3 1.3 1.3
Borax 4 4 4
Sodium citrate 7 7 7
Sodium chloride 4 4 4 t Ethanol 30 30 O*
Water balance to
Triolein removal was:
Example 13 s ulphosuccinate only 2.1
Example 14 s ulphosuccinate nonionic 45.7
Example 15 n onionic only 3.1
The synergy between the dialkylsulphosuccinate and
the nonionic surfactant is apparent.
L-

Claims (1)

  1. Y
    19
    THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:
    1. A detergent composition comprising:
    1 to 50% by weight of a surfactant system which is a mixture
    of:
    i) dialkylsulphosuccinate, the alkyl substituent groups of
    which contain at least 4 carbon atoms each and contain 12 to
    20 carbon atoms in total; and o* o It
    ii) an alkoxylated nonionic surfactant which has an HLB value not above 10.5;
    the ratio of i) to ii) lying between 7:1 and 1:7, and
    to 60% by weight of detergency builder.
    2. A composition according to claim 1 wherein the
    ratio of i) to ii) lies between 4:1 and 1:4.
    i 3. A composition according to claim 1 or claim 2
    wherein at least half of the sulphosuccinate has alkyl
    groups with a total of 12 to 16 carbon atoms.
    4. A composition according to claim 1, claim 2 or
    claim 3 wherein at least half of the sulphosuccinate has
    both alkyl groups the same.
    71 7
    A composition according to claim 4 wherein at
    least half of the sulphosuccinate has alkyl groups
    containing 7 carbon atoms in straight chain formations.
    6. A composition according to any one of the
    preceding claims containing at least 10% by weight of
    detergency builder. o
    o oe
    0 7. A composition according to any one of the 9 0
    oo preceding claims containing at least 10% by weight of water-
    soluble electrolyte.
    8. A composition according to any one of the 15 preceding claims in which the nonionic surfactant has an HLB
    of less than
    9. A composition according to any one of the
    preceding claims which contains sufficient alkaline salt to
    render a pH of at least 6, when the composition is added to t
    distilled water at 25°C in an amount of 1 g/litre or more.
    A composition according to any one of the
    preceding claims which is a granular composition suitable for washing fabrics.
    L-2: 2
    ~-Tc~ r
    t
    11. A composition according to any one of the
    preceding claims which contains at least one of:
    fabric softening agents
    fabric softening clay
    lather booster
    lather depressant
    bleaching agent
    fluorescent agent 0 oo perfume, and 0, o oo enzyme.
    t
    04 r
    0440c 12. A method of washing which comprises contacting soiled material with a built aqueous wash liquor which is a II solution of surfactant system comprising a mixture or:
    00 4 i) dialkylsulphosuccinate, the alkyl substituent groups of 0I which contain at least 4 carbon atoms each and contain 12 to *040
    044 4~r 20 carbon atoms in total; and
    0000« 20 ii) an alkoxylated nonionic surfactant which has an HLB 04 ti value not above 10.5;
    the ratio of i) to ii) lying between 7:1 and 1:7.
    13. A method according to claim 12 wherein the ratio of i) to ii) lies between 4:1 and 1:4.
    14. A method according to claim 12 or claim 13 wherein
    Lm- 1
    -C l U1
    22
    at least half of the sulphosuccinate has alkyl groups with a
    total of 12 to 16 carbon atoms.
    A method according to claim 12, claim 13 or claim
    14 wherein at least half of the sulphosuccinate has both
    alkyl groups the same.
    o* 16. A method according to claim 15 wherein at least
    half of the sulphosuccinate has alkyl groups containing 7
    10 carbon atoms in straight chain formations.
    17. A method according to any one of claims 12 to 16
    wherein the wash liquor contains electrolyte to give an
    electrolyte concentration of at least 0.01 molar.
    18. A method according to any one of claims 12 to 17
    Swherein the wash liquor has a pH of at least 6.
    19. A method according to any one of claims 12 to 18
    wherein the nonionic surfactant has an HLB of less than
    DATED THIS 10TH DAY OF OCTOBER 1989 UNILEVER PLC By its Patent Attorneys:
    GRIFFITH HACK CO. Fellows Institute of Patent Attuoneys of Australia.
    -"In V
AU42707/89A 1988-10-20 1989-10-10 Detergent composition Ceased AU622932B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888824599A GB8824599D0 (en) 1988-10-20 1988-10-20 Detergent composition
GB8824599 1988-10-20

Publications (2)

Publication Number Publication Date
AU4270789A true AU4270789A (en) 1990-04-26
AU622932B2 AU622932B2 (en) 1992-04-30

Family

ID=10645515

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (6)

Country Link
EP (1) EP0365184A3 (en)
JP (1) JPH02158700A (en)
AU (1) AU622932B2 (en)
BR (1) BR8905310A (en)
GB (1) GB8824599D0 (en)
ZA (1) ZA897668B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5531939A (en) * 1994-03-23 1996-07-02 Amway Corporation Concentrated glass and window cleaning composition and method of use

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3910855A (en) * 1972-05-16 1975-10-07 Richard M Abeles Liquid cleaning compositions
GB8301745D0 (en) * 1983-01-21 1983-02-23 Unilever Plc Detergent compositions
GB8311854D0 (en) * 1983-04-29 1983-06-02 Unilever Plc Detergent compositions
GB8824600D0 (en) * 1988-10-20 1988-11-23 Unilever Plc Detergent composition

Also Published As

Publication number Publication date
GB8824599D0 (en) 1988-11-23
JPH02158700A (en) 1990-06-19
EP0365184A2 (en) 1990-04-25
EP0365184A3 (en) 1991-08-07
ZA897668B (en) 1991-06-26
BR8905310A (en) 1990-05-22
AU622932B2 (en) 1992-04-30

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