WO1997032965A1 - Composition of washing bars - Google Patents

Composition of washing bars Download PDF

Info

Publication number
WO1997032965A1
WO1997032965A1 PCT/EP1996/005878 EP9605878W WO9732965A1 WO 1997032965 A1 WO1997032965 A1 WO 1997032965A1 EP 9605878 W EP9605878 W EP 9605878W WO 9732965 A1 WO9732965 A1 WO 9732965A1
Authority
WO
WIPO (PCT)
Prior art keywords
acid
composition
weight
water soluble
soap
Prior art date
Application number
PCT/EP1996/005878
Other languages
French (fr)
Inventor
Milind Vinayak Bhandarh
Dhanraj Kalyansundaram Chokappa
Velayudhan Nair Gopa Kumar
Devadatta Shivaji Sankholkar
Original Assignee
Unilever Plc
Unilever N.V.
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, Unilever N.V. filed Critical Unilever Plc
Priority to AU13081/97A priority Critical patent/AU1308197A/en
Priority to BR9612536A priority patent/BR9612536A/en
Priority to PL96328764A priority patent/PL184540B1/en
Publication of WO1997032965A1 publication Critical patent/WO1997032965A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/006Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3761(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines

Definitions

  • This invention relates to compositions of washing bars for personal or fabric washing.
  • the invention particularly relates to compositions with higher water content but retaining the mechanical, structural aspects for satisfactory processability and end user properties such as better feel, lathering, lower sog/mush and satisfactory cleaning.
  • Yield stress needed to cause a flow in a material is of fundamental importance in determining the structural stability and integrity of multiphase composites such as soaps and detergents. Yield stress plays a major role in the processability of soaps and detergents especially in soap processing equipment such as roll mills, plodders, stampers etc.
  • Milled bars typically have a water content of between 8-15% while 'hard' (non-milled) soap bars have water content in the re,-ion of 20-35%. Increase in the water content can replace the TFM making it more economical but will tend to soften the soap bar.
  • GB 2,230,022 discloses the use of polyacrylate and citrate as barrier materials to improve the softening of the washed fabric by clay n detergent powder formulations.
  • US 5,279,756 discloses the use of acrylic polymers and carboxylic acids as sequestering agents in dish washing compositions.
  • BR 8905598 discloses the use of two specific polymers namely acrylic polymer CO-1 (Acrysol MW-400N) , Rohm and Haas, and Acrysol ASE-75 of Rohm and Haas with a molecular weight of 40,000 to make the bar harder, improve foaming and skin feel. It further specifies that 'high molecular weight acrylic polymers are used because the higher viscosity of the liquid will make more distinct striations and, since the acrylic polymer is on the surface, provides better lubricity to hands during washing with the detergent bar' .
  • the compositions disclosed m this patent are of fairly low water concentrations where hardening s not a problem.
  • the present invention differs from the prior art in that it addresses the problem of producing bars with high water content which normally would be soft and pose acute problems in processing and unsatisfactory end use.
  • compositions with higher water content but retaining the appropriate structural properties and processability.
  • the composition would also have enhanced physical properties such as higher yield stress, lathering, better feel, lower sog/mush and satisfactory cleaning.
  • the present invention s directed to improved washing formulations with higher water content but retaining superior physical properties such as mechanical, structural aspects for satisfactory processability and end user properties such as better feel, lathering, lower sog/mush and satisfactory cleaning, by way of incorporation of a synergistic additives comprising of water soluble anionic polymers and/or copolymers, having a molecular weight range 500-30,000, in the range of 0.05 to 5% by weight of the formulation and may optionally comprise of one or more of carboxylated compounds at concentrations upto 5% by weight of the total formulation.
  • a synergistic additives comprising of water soluble anionic polymers and/or copolymers, having a molecular weight range 500-30,000, in the range of 0.05 to 5% by weight of the formulation and may optionally comprise of one or more of carboxylated compounds at concentrations upto 5% by weight of the total formulation.
  • a washing composition with higher water content but retaining excellent yield stress, improved lathering, feel and satisfactory cleaning comprising:
  • the actives in the composition is provided by neat soap obtained from saponification of oils/fats such as rice bran, tallow, palm, castor, groundnut, palm kernel, cotton seed, soybean, coconut etc. or their respective fatty acids and/or any of the synthetic detergents.
  • oils/fats such as rice bran, tallow, palm, castor, groundnut, palm kernel, cotton seed, soybean, coconut etc. or their respective fatty acids and/or any of the synthetic detergents.
  • the water soluble anionic polymers that can be used in the formulations according to the invention include polyacrylic acid, polymethacrylic acid, polystyrene sulphonic acid, acrylic acid-maleic acid copolymers etc.
  • Suitable water soluble copolymers include combination of monomers, at least one of which contains hydrophilic groups like sulphonic acid, sulphate or carboxylic acid or their salts, e.g. acyrlamide-acrylic/methacrylic acid copolymers, polyacrylamide maleic acid copolymers, acrylic/methacrylic acid copolymers.
  • the above water soluble anionic polymers and water soluble co-polymers is selected to have a molecular weight range 500- 30,000.
  • the preferred water soluble anionic polymer is polyacrylic acid in the molecular weight range 500-5000.
  • the carboxylated compounds preferably are citric acid, lactic acid and maleic acid.
  • the Carri-Med Rheometer being a controlled stress rheometer can be used to measure the yield stress of materials under shear conditions.
  • the controlled stress rheometer can apply stresses as low as 0.07 Pa and the stress value at which flow is initiated is a direct measure of the yield stress of the material (strain rate is measured) .
  • Carri-Med rheometer model CSLIOO was used with a cone and plate fixture having a 2cm diameter and an angle of 1°58' . The measurements were carried out at 40°C.
  • the maximum yield stress that can be measured on this instrument is 6300 pa. and the minium detectable strain rate is about 10 "e sec "1 .
  • the soap base (300 g) containing 30% coconut oil fatty acid salt, balance being the salts of distilled fatty acids derived from a mixture of oils (e.g. rice bran/palm) of moisture content 10.8% was taken in an autoclave and heated to 50°C. 83ml of water was added to it and the soap was stirred and heated to 95°C for 3hrs. The soap melt was fed slowly into another chamber below the autoclave which was maintained under vacuum. The vacuum dried soap (moisture 27%) was cooled to 25-30°C, passed through a triple roll mill and plodded into bars .
  • the milled soap mentioned above were dried in an air oven (40-45°C) before plodding for making soaps with lower moisture contents.
  • the soap base (300g) was prepared as in the case of control but a mixture containing 1 g, sodium hydroxide, 1.5 g. polyacrylic acid (PAA) (SOKOLAN PA ex. BASF, mol .w .1500) and 1.5g. citric acid dissolved in 83 ml of water was added to the soap in the autoclave. The soap was stirred and heated to 95°C for 3hrs. The soap melt was fed slowly into another chamber below the autoclave maintained under vacuum. The vacuum dried soap was cooled to 25-30°C, passed through a triple roll mill and plodded into bars.
  • PAA polyacrylic acid
  • citric acid dissolved in 83 ml of water
  • the milled soap mentioned above were dried in an air oven (40-45°C) before plodding for making soaps with lower moisture contents.
  • the samples as per Example a and b were subjected to yield stress and penetration tests following the method described herein.
  • the apparatus consists of a cheesewire attached to a counter balanced arm which can pivot freely via a ball race bearing.
  • a billet of soap s positioned under the wire such that the wire is just in contact with one edge of the billet.
  • W g. weight
  • the area over which the force acts will increase as the depth of cut increases and therefore the stress being exerted w ll decrease until it is exactly balanced by resistance of the soap and the wire stops moving.
  • the stress at this point is equal to the yield stress of the soap.
  • the time taken to reach this point was found to be 30 sees, so that a standard t me of 1 min was chosen to ensure that the yield stress had been reached. After this time the weight was removed and the length of the cut measured.
  • the yield stress is calculated using the semi-empirical formula :
  • a pointed metal cone of specified dimensions is allowed to penetrate into the bar using standard weight on the top of the cone.
  • the cone penetrates the bar upto a certain depth till the downward force due to weight balances with the upward force due to the drag.
  • the depth is measured in units of 1/10 of a mm. Higher penetration means lower yield stress .
  • Citric acid - - 1 0.5
  • the soap comprised of 30% coconut oil fatty acid salt, balance being the salts of distilled fatty acid derived from a mixture of oils (eg. rice bran/palm) .
  • the soap contained 30% water to which various ingredients (PAA, citric acid, perfume etc.) were added and the mixture dried to the final moisture content indicated in Table 4.
  • a set of bars is used to wash in a standard manner once daily by each operator and drained after each wash, for five days. After two further non-washing days, % wear is determined as weight loss. This is a standardised simulation of use.
  • the test involves a panel of volunteers who wash their hands with the test tablets once during the test.
  • the hand wash is performed 24° French hard (FH) water in a bowl and volume of lather produced is measured.
  • FH French hard
  • a set of bars is used to wash in a standard manner once daily by each operator for five days. From the second day onwards, the depth of the mush on the bar is evaluated by trained assessor using a calibrated scale in mm. The values over 5 days are monitored and the final day value is reported. This is a standardised simulation of use.
  • the data presented in Table 4 shows that the experimental bar has significantly higher yield stress and other in use properties .
  • the present invention is directed provide for improved soap/detergent formulations having higher water content but retaining the mechanical, structural aspects for satisfactory processability and end user properties such as better feel, lathering, lower sog/mush and satisfactory cleaning.

Landscapes

  • 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)

Abstract

A composition for personal or fabric washing comprises: (i) 25 to 70 % by weight of surfactant active; (ii) 0.05 to 5 % by weight of water-soluble anionic polymer and/or copolymer having a molecular weight of from 500 to 30,000; (iii) 15 to 50 % by weight of water; and (iv) other additives making up the total balance. Such a composition is particularly suited for producing bars with high water content whilst retaining structural properties and processability. Enhanced physical properties such as higher yield stress, lathering and lower mush are also attained.

Description

COMPOSITION OF WASHING BARS
This invention relates to compositions of washing bars for personal or fabric washing. The invention particularly relates to compositions with higher water content but retaining the mechanical, structural aspects for satisfactory processability and end user properties such as better feel, lathering, lower sog/mush and satisfactory cleaning.
Background and prior art
Conventional detergent bars based on soap for personal washing contains over about 70% by weight total fatty matter (TFM) , the remainder being water (about 10-20%) and other ingredients e.g. colour, perfume, preservatives etc. Many particulate materials may also be present which replace some of the soap in the bar while retaining satisfactory processability.
Yield stress needed to cause a flow in a material is of fundamental importance in determining the structural stability and integrity of multiphase composites such as soaps and detergents. Yield stress plays a major role in the processability of soaps and detergents especially in soap processing equipment such as roll mills, plodders, stampers etc.
Milled bars typically have a water content of between 8-15% while 'hard' (non-milled) soap bars have water content in the re,-ion of 20-35%. Increase in the water content can replace the TFM making it more economical but will tend to soften the soap bar. GB 2,230,022 discloses the use of polyacrylate and citrate as barrier materials to improve the softening of the washed fabric by clay n detergent powder formulations. US 5,279,756 discloses the use of acrylic polymers and carboxylic acids as sequestering agents in dish washing compositions. BR 8905598 discloses the use of two specific polymers namely acrylic polymer CO-1 (Acrysol MW-400N) , Rohm and Haas, and Acrysol ASE-75 of Rohm and Haas with a molecular weight of 40,000 to make the bar harder, improve foaming and skin feel. It further specifies that 'high molecular weight acrylic polymers are used because the higher viscosity of the liquid will make more distinct striations and, since the acrylic polymer is on the surface, provides better lubricity to hands during washing with the detergent bar' . The compositions disclosed m this patent are of fairly low water concentrations where hardening s not a problem.
The present invention differs from the prior art in that it addresses the problem of producing bars with high water content which normally would be soft and pose acute problems in processing and unsatisfactory end use.
It is the basic objective of the present invention to provide for washing compositions with higher water content but retaining the appropriate structural properties and processability. The composition would also have enhanced physical properties such as higher yield stress, lathering, better feel, lower sog/mush and satisfactory cleaning.
Definition of the Invention
Thus the present invention s directed to improved washing formulations with higher water content but retaining superior physical properties such as mechanical, structural aspects for satisfactory processability and end user properties such as better feel, lathering, lower sog/mush and satisfactory cleaning, by way of incorporation of a synergistic additives comprising of water soluble anionic polymers and/or copolymers, having a molecular weight range 500-30,000, in the range of 0.05 to 5% by weight of the formulation and may optionally comprise of one or more of carboxylated compounds at concentrations upto 5% by weight of the total formulation.
Description of the Invention
According to this invention, there is provided a washing composition with higher water content but retaining excellent yield stress, improved lathering, feel and satisfactory cleaning comprising:
(i) 25 to 70% by weight of soap/detergent actives (ii) 0.05 to 5% by weight of water soluble anionic polymers and/or copolymers, having a molecular weight range 500-30,000,
(iii) optionally upto 5% of carboxylated compounds (iv) 15 to 50% by weight of water and balance being other additives.
The actives in the composition is provided by neat soap obtained from saponification of oils/fats such as rice bran, tallow, palm, castor, groundnut, palm kernel, cotton seed, soybean, coconut etc. or their respective fatty acids and/or any of the synthetic detergents.
The water soluble anionic polymers that can be used in the formulations according to the invention include polyacrylic acid, polymethacrylic acid, polystyrene sulphonic acid, acrylic acid-maleic acid copolymers etc. Suitable water soluble copolymers include combination of monomers, at least one of which contains hydrophilic groups like sulphonic acid, sulphate or carboxylic acid or their salts, e.g. acyrlamide-acrylic/methacrylic acid copolymers, polyacrylamide maleic acid copolymers, acrylic/methacrylic acid copolymers.
The above water soluble anionic polymers and water soluble co-polymers is selected to have a molecular weight range 500- 30,000. The preferred water soluble anionic polymer is polyacrylic acid in the molecular weight range 500-5000.
The carboxylated compounds preferably are citric acid, lactic acid and maleic acid.
It is found by way of this invention that a synergistic effect is achieved in as far as increasing the water content of the soap formulations while retaining the physical properties of the soap in use of the above synergistic additives in soap formulations in the selected range as proposed above.
The nature of invention, its object and advantages will be further apparent form the ensuing description made with relation to non-limiting exemplary control formulation without the synergistic additive discussed above and formulations according to the invention including such synergistic additives.
EXAMPLES
EXAMPLE 1
Sodium oleate soap containing 30% moisture (Control) and the soap containing polyacrylic acid of different molecular weights were prepared and yield stress (Carri-Med Rheometer) was measured.
Yield Stress Measurement
The Carri-Med Rheometer being a controlled stress rheometer can be used to measure the yield stress of materials under shear conditions. The controlled stress rheometer can apply stresses as low as 0.07 Pa and the stress value at which flow is initiated is a direct measure of the yield stress of the material (strain rate is measured) . Carri-Med rheometer model CSLIOO was used with a cone and plate fixture having a 2cm diameter and an angle of 1°58' . The measurements were carried out at 40°C. The maximum yield stress that can be measured on this instrument is 6300 pa. and the minium detectable strain rate is about 10"e sec"1.
Date presented in Table 1 shows effect of molecular weight of PAA on yield stress.
Table 1
Ingredients in formulation Yield Stress, Pa.
Sodium oleate (Active) 784
Active + 5% PAA (MW) 90,000 550
Active + 5% PAA (MW) 5000 932
Active + 5% PAA (MW) 2000 1880
MW=Molecular weigh .
The data presented in Table 1 shows that lower molecular weight PAA are better in improving the yield stress of the soap. EXAMPLE 2
EXAMPLE a: Control formulation
The soap base (300 g) containing 30% coconut oil fatty acid salt, balance being the salts of distilled fatty acids derived from a mixture of oils (e.g. rice bran/palm) of moisture content 10.8% was taken in an autoclave and heated to 50°C. 83ml of water was added to it and the soap was stirred and heated to 95°C for 3hrs. The soap melt was fed slowly into another chamber below the autoclave which was maintained under vacuum. The vacuum dried soap (moisture 27%) was cooled to 25-30°C, passed through a triple roll mill and plodded into bars .
The milled soap mentioned above were dried in an air oven (40-45°C) before plodding for making soaps with lower moisture contents.
EXAMPLE b: Experimental formulation
The soap base (300g) was prepared as in the case of control but a mixture containing 1 g, sodium hydroxide, 1.5 g. polyacrylic acid (PAA) (SOKOLAN PA ex. BASF, mol .w .1500) and 1.5g. citric acid dissolved in 83 ml of water was added to the soap in the autoclave. The soap was stirred and heated to 95°C for 3hrs. The soap melt was fed slowly into another chamber below the autoclave maintained under vacuum. The vacuum dried soap was cooled to 25-30°C, passed through a triple roll mill and plodded into bars.
The milled soap mentioned above were dried in an air oven (40-45°C) before plodding for making soaps with lower moisture contents. The samples as per Example a and b were subjected to yield stress and penetration tests following the method described herein.
Yield Stress Measurement
The apparatus consists of a cheesewire attached to a counter balanced arm which can pivot freely via a ball race bearing. A billet of soap s positioned under the wire such that the wire is just in contact with one edge of the billet. By applying a weight (W g.) directly above the cheesewire a constant force is exerted on the wire which w ll slice into the soap. The area over which the force acts will increase as the depth of cut increases and therefore the stress being exerted w ll decrease until it is exactly balanced by resistance of the soap and the wire stops moving. The stress at this point is equal to the yield stress of the soap. The time taken to reach this point was found to be 30 sees, so that a standard t me of 1 min was chosen to ensure that the yield stress had been reached. After this time the weight was removed and the length of the cut measured.
The yield stress is calculated using the semi-empirical formula :
Y.S = 3 W x 98.1 Pascal (Pa.) 8 1 x d
The penetration test
A pointed metal cone of specified dimensions is allowed to penetrate into the bar using standard weight on the top of the cone. The cone penetrates the bar upto a certain depth till the downward force due to weight balances with the upward force due to the drag. The depth is measured in units of 1/10 of a mm. Higher penetration means lower yield stress .
Table 2
%Moisture Example a Penetration Example b Penetration YS*xl05 value YS*xlOb value
27 1.8 45 3.7 33
22 4.2 31 7.4 22
17 7.3 15 9.8 17
*YS=Yield stress in Pa.
The data presented in Table 2 clearly show that soaps containing the synergistic additive of the invention (Example b) has a significantly higher yield stress indicating that the presence of the additive results in soap bars which are processable by the milled route in spite of higher moisture conten .
EXAMPLE 3
Soap (Sodium oleate) formulations as indicated in Table 3 were prepared and the data on yield stress was measured as per the procedure described as in Example 1.
Ingredients Example c Example d Examp1e e Example f (%)
Soap 73 72 72 72
PAA - 1 - 0.5
Citric acid - - 1 0.5
Water 27 27 27 27
Yield 573 1389 1018 >6360 stress P.a The data on yield stress presented in Table 3 shows that even when Polyacrylic acid (PAA) and citric acid are added at 0.5% each in the formulation they give a synergistic effect and show that the yield stress is enhanced far greater than when PAA or citric acid is used alone at 1% level.
EXAMPLE 4
Control and experimental bars as per the formulation described in Table 4 were prepared and data on yield stress (measured as described in Example 2), rate of wear, lather, mush and feel were recorded. The soap comprised of 30% coconut oil fatty acid salt, balance being the salts of distilled fatty acid derived from a mixture of oils (eg. rice bran/palm) . The soap contained 30% water to which various ingredients (PAA, citric acid, perfume etc.) were added and the mixture dried to the final moisture content indicated in Table 4.
Rate of wear
A set of bars is used to wash in a standard manner once daily by each operator and drained after each wash, for five days. After two further non-washing days, % wear is determined as weight loss. This is a standardised simulation of use.
Lather
The test involves a panel of volunteers who wash their hands with the test tablets once during the test. The hand wash is performed 24° French hard (FH) water in a bowl and volume of lather produced is measured. A standard washing procedure in cold water followed by estimation of feel by a trained observer.
Mush
A set of bars is used to wash in a standard manner once daily by each operator for five days. From the second day onwards, the depth of the mush on the bar is evaluated by trained assessor using a calibrated scale in mm. The values over 5 days are monitored and the final day value is reported. This is a standardised simulation of use.
Table 4
Ingredients (%) Control Experimental
Soap 84.2 79.9
PAA 0 0.5
Citric acid 0 0.5
Moisture 14.0 17.3
Perfume etc. 1.8 1.8
Water/soap 0.17 0.22
Yield stress (106 Pa) 2.8 3.3
% Rate of wear 39.6 42.4
Lather(24° FH) 174.0 186.0
Mush 5.7 4.0
Feel Satisfactory Superior
The data presented in Table 4 shows that the experimental bar has significantly higher yield stress and other in use properties . Thus the present invention is directed provide for improved soap/detergent formulations having higher water content but retaining the mechanical, structural aspects for satisfactory processability and end user properties such as better feel, lathering, lower sog/mush and satisfactory cleaning.

Claims

1. A composition for personal or fabric washing comprising:
(i) 25 to 70% by weight of surfactant active;
(ii) 0.05 to 5% by weight of water soluble anionic polymer and/or copolymer having a molecular weight of from 500 to 30,000; (iii) 15 to 50% by weight of water; and (iv) other additives making up the total balance.
2. A composition as claimed in claim 1, further comprising up to 5% by weight of a carboxylated compound.
3. A composition as claimed in either claim 1 or claim 2, wherein the surfactant active is either
(i) a synthetic detergent;
(ii) a neat soap obtainable from saponification of oils or fats; or
(iii) mixtures thereof.
4. A composition as claimed in claim 3, wherein the oils or fats are rice bran, tallow, palm castor, groundnut, palm kernel, cotton seed, soybean or coconut.
5. A composition as claimed in any preceding claim, wherein the water soluble anionic polymer is polyacrylic acid, polymethacrylic acid, polystyrene sulphonic acid or acrylic acid/ aleic acid copolymer.
6. A composition as claimed in any of claims 1-4 wherein the water soluble anionic polymer is a combination of monomers at least one of which contains a hydrophilic group, preferably sulphonic acid, sulphuric acid, 13
carboxylic acid or salts thereof.
7. A composition as claimed in claim 6, wherein the water soluble polymer is acrylamide-acrylic/methacrylic acid copolymer, polyacrylamide maleic acid copolymer or acrylic/methacrylic acid copolymer.
8. A composition as claimed in any of claims 1-4, wherein the water soluble polymer is polyacrylic acid of molecular weight from 500 to 5000.
9. A composition as claimed m any of claims 2-8, wherein the carboxylated compound is citric acid, lactic acid or maleic acid.
PCT/EP1996/005878 1996-03-04 1996-12-20 Composition of washing bars WO1997032965A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
AU13081/97A AU1308197A (en) 1996-03-04 1996-12-20 Composition of washing bars
BR9612536A BR9612536A (en) 1996-03-04 1996-12-20 Composition for personal or fabric washing
PL96328764A PL184540B1 (en) 1996-03-04 1996-12-20 Compositions of solid washing agent in the form of bars or blocks

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9604585.1A GB9604585D0 (en) 1996-03-04 1996-03-04 Composition
GB9604585.1 1996-03-04

Publications (1)

Publication Number Publication Date
WO1997032965A1 true WO1997032965A1 (en) 1997-09-12

Family

ID=10789824

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1996/005878 WO1997032965A1 (en) 1996-03-04 1996-12-20 Composition of washing bars

Country Status (10)

Country Link
CN (1) CN1170919C (en)
AU (1) AU1308197A (en)
BR (1) BR9612536A (en)
CZ (1) CZ292063B6 (en)
GB (1) GB9604585D0 (en)
HU (1) HUP9904128A3 (en)
PL (1) PL184540B1 (en)
TR (1) TR199801276T2 (en)
WO (1) WO1997032965A1 (en)
ZA (1) ZA97146B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11352594B2 (en) 2019-02-19 2022-06-07 Conopco, Inc. Extruded soap bar with high water content
US11473038B2 (en) 2019-02-19 2022-10-18 Conopco, Inc. High water hard bars comprising combination of type and amount of electrolytes

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110021410A1 (en) * 2009-07-27 2011-01-27 Ecolab Usa Inc. Novel formulation of a ware washing solid controlling hardness

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB935733A (en) * 1961-03-16 1963-09-04 Basf Ag Detergents and cleaning products
GB1333042A (en) * 1969-08-22 1973-10-10 Unilever Ltd Detergent bars
EP0186148A2 (en) * 1984-12-24 1986-07-02 The B.F. GOODRICH Company Toilet soap containing polymeric thickener
GB2238316A (en) * 1989-11-24 1991-05-29 Unilever Plc Soap bars
WO1994019442A1 (en) * 1993-02-20 1994-09-01 The Boots Company Plc Toiletries composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB935733A (en) * 1961-03-16 1963-09-04 Basf Ag Detergents and cleaning products
GB1333042A (en) * 1969-08-22 1973-10-10 Unilever Ltd Detergent bars
EP0186148A2 (en) * 1984-12-24 1986-07-02 The B.F. GOODRICH Company Toilet soap containing polymeric thickener
GB2238316A (en) * 1989-11-24 1991-05-29 Unilever Plc Soap bars
WO1994019442A1 (en) * 1993-02-20 1994-09-01 The Boots Company Plc Toiletries composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11352594B2 (en) 2019-02-19 2022-06-07 Conopco, Inc. Extruded soap bar with high water content
US11473038B2 (en) 2019-02-19 2022-10-18 Conopco, Inc. High water hard bars comprising combination of type and amount of electrolytes

Also Published As

Publication number Publication date
TR199801276T2 (en) 1998-09-21
CZ292063B6 (en) 2003-07-16
CZ281398A3 (en) 1999-02-17
HUP9904128A3 (en) 2001-11-28
AU1308197A (en) 1997-09-22
HUP9904128A2 (en) 2000-04-28
GB9604585D0 (en) 1996-05-01
ZA97146B (en) 1998-07-08
PL328764A1 (en) 1999-02-15
CN1170919C (en) 2004-10-13
BR9612536A (en) 1999-07-20
CN1200761A (en) 1998-12-02
PL184540B1 (en) 2002-11-29

Similar Documents

Publication Publication Date Title
US5952289A (en) Soap-based laundry bars with improved firmness
US5328632A (en) Low pH mild personal cleansing bar with lathering mild synthetic surfactant and magnesium soap
CN102939368B (en) Low tmf extruded soap bars having reduced cracking
US4110239A (en) Quick lathering toilet bars and method of making same
WO2010089269A1 (en) Low tmf extruded soap bars comprising polysacharide-polyol structuring system
EP0089714A1 (en) Process for making high-glycerin soap bars
US5998341A (en) Bar composition comprising water-soluble anionic polymer and/or copolymer
CA1304270C (en) Cleaning compositions with skin protection agents
WO1997032965A1 (en) Composition of washing bars
CA1117393A (en) Detergent bars with improved properties
NO744706L (en)
EP0575440B1 (en) LOW pH MILD PERSONAL CLEANSING BAR
US3989647A (en) Quick lathering toilet bars and method of making same
KR920002114B1 (en) Detergent bars
US20050043195A1 (en) Dishwashing compositions comprising floating particles
EP1476532B1 (en) Soap bar comprising high levels of specific alkoxylated triglycerides
CA2449803A1 (en) Soap composition
US3278444A (en) Detergent composition
KR100819227B1 (en) Soap bar comprising triglycerides and processes therefor
Ginn et al. Effect of tallow‐coconut fatty acid ratios on properties of bar soaps
US4058487A (en) Quick lathering toilet bars and method of making same
WO2000042159A1 (en) Detergent bar composition
GB2110711A (en) Soap bars
RO114345B1 (en) Soap composition containing sodium pyrophosphate and method for producing the same
JP2007070414A (en) Bar soap

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 96197941.0

Country of ref document: CN

AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GE HU IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK TJ TM TR TT UA UG UZ VN AM AZ BY KG KZ MD RU TJ TM

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): KE LS MW SD SZ UG AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
CFP Corrected version of a pamphlet front page
CR1 Correction of entry in section i

Free format text: PAT.BUL.39/97 UNDER INID (71) "APPLICANT (FOR ALL DESIGNATED STATES EXCEPT AU,BB,CA,GB,IE,IL,KE,LC,LK,LS,MN,MW,NZ,SD,SG,SZ,TT,UG)",THE APPLICANT'S NAME SHOULD READ "UNILEVER N.V."

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 1998/01276

Country of ref document: TR

WWE Wipo information: entry into national phase

Ref document number: PV1998-2813

Country of ref document: CZ

NENP Non-entry into the national phase

Ref document number: 97531380

Country of ref document: JP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: PV1998-2813

Country of ref document: CZ

NENP Non-entry into the national phase

Ref country code: CA

122 Ep: pct application non-entry in european phase
WWG Wipo information: grant in national office

Ref document number: PV1998-2813

Country of ref document: CZ