WO2003068901A1 - Detergent en pain et son procede de fabrication - Google Patents
Detergent en pain et son procede de fabrication Download PDFInfo
- Publication number
- WO2003068901A1 WO2003068901A1 PCT/EP2003/000625 EP0300625W WO03068901A1 WO 2003068901 A1 WO2003068901 A1 WO 2003068901A1 EP 0300625 W EP0300625 W EP 0300625W WO 03068901 A1 WO03068901 A1 WO 03068901A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- detergent
- active
- alkali
- neutralised
- phosphate
- Prior art date
Links
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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/006—Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/0065—Solid detergents containing builders
- C11D17/0069—Laundry bars
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
-
- 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
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/06—Inorganic compounds
- C11D9/08—Water-soluble compounds
- C11D9/10—Salts
- C11D9/14—Phosphates; Polyphosphates
-
- 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
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/26—Organic compounds, e.g. vitamins containing oxygen
Definitions
- the invention relates to a synergistic composition of soap/detergent bars for personal and/or fabric washing. It also relates to a process for the preparation of such soap/detergent bars for personal and/or fabric washing. In particular, the invention is directed towards the suppression of efflorescence in detergent bars comprising a detergent active and one or more phosphates.
- Conventional detergent bars for personal and fabric washing usually contain a detergent active, water and other ingredients such as colour, perfume, preservatives, etc.
- Structurants and fillers are also present in such compositions, which replace some of the active in the bar while retaining the desired hardness of the bar.
- a few known structurants and fillers include starch, kaolin, silicates and talc.
- Bars meant for personal wash are based on soap, and are either milled or non-milled.
- Hard non-milled soap bars typically contain 20-35% moisture, while milled bars typically have a moisture content of 8-15%.
- Unstructured hard non-milled soap bars will usually have a total fatty matter (TFM) of 55-60%, whilst unstructured milled soap bars typically have a TFM of 75-80%.
- TFM total fatty matter
- Reduction in TFM requires that the bar be 'structured' by the use of insoluble particulate materials like kaolin and talc and/or soluble silicates .
- Orthophosphates and pyrophosphates are used in soap bar compositions. The phosphates help in reducing TFM, increasing the moisture content of the bar, and also act as builders. While it is advantageous to incorporate phosphates, their use in the soap system creates problems like efflorescence that impairs the visual appearance of the bar.
- US 6310016 (Unilever Home & Personal Care USA) discloses a low total fatty matter detergent bar composition comprising 15-70% total fatty matter, 0.5-40% colloidal aluminium hydroxide-phosphate complex and 10-50% water wherein the phosphate is generated from orthophosphoric acid.
- Electrolytes suitable for the invention include simple and condensed potassium phosphates as well as electrolytes chosen from sodium and/or potassium citrates, acetates, formates and tartarates .
- soap bars containing phosphates have a higher pH than conventional soap bars.
- the high pH causes problems like skin irritation and dryness, particularly amongst users with sensitive skin.
- the pH is conventionally adjusted by adding free fatty acid.
- These "superfatted” phosphate structured bars show enhanced efflorescence.
- “superfatted” is meant bars that contain free fatty acid. The aforesaid problem is also not addressed in the prior art .
- a detergent bar comprising the detergent active, phosphates and a water soluble organic salt shows synergistic benefits of minimal or no efflorescence during storage.
- efflorescence is significantly reduced for soap bars that are superfatted and phosphate structured.
- the invention also relates to a process to make these bars .
- the present invention relates to detergent bar compositions comprising a detergent active, one or more hydrated phosphates and one or more water-soluble salts of organic acids.
- the detergent bar of the invention shows minimal or no efflorescence.
- the detergent bar comprises soap.
- the invention is useful for "superfatted" soap bars comprising soap, hydrated phosphates and water soluble salts of organic acids.
- the invention also relates to a process to make the synergistic detergent bars of the invention.
- a detergent bar composition comprising:
- anhydrous component of hydrated phosphate is up to 20% phosphorus pentoxide (P 2 O 5 ) .
- the detergent active comprises a soap.
- the phosphate and the soap may be generated in situ consecutively or simultaneously, or prepared independently and mixed.
- synergistic detergent bar composition comprising:
- anhydrous component of hydrated phosphate is up to 20% P 2 O 5 . It is particularly preferred that the alkali used in the soap formation contains aluminium. Sodium aluminate is especially preferred.
- synergistic detergent bar composition comprising:
- anhydrous component of hydrated phosphate is up to 20% P 2 O 5 .
- compositions according to the invention may have the anhydrous component of the hydrated phosphate contain up to 25% P 2 0 5 .
- the anhydrous component of the hydrated phosphate may in some instances typically contain at least 0.1%, sometimes at least 0.5%, maybe at least 1% and in others at least 5% of P 2 0 5 . In some circumstances at least 10% P 2 0 5 may be present. It is further preferred that up to 5% free fatty acid is present in the detergent bar of the invention.
- Especially preferred fatty acids have a carbon chain length of C8-C14.
- step (c) converting the product of step (c) into bars by a known method.
- an improved process for preparing a synergistic detergent bar composition as described herein which process comprises the steps of:
- step (c) a. generating phosphate by reacting phosphorus containing mineral acid with an alkali in presence of soap and optionally other detergent active precursors at a temperature between 25°C to 105°C to obtain a mixture of phosphate and soap; generating in or adding to the soap the water soluble salt of an organic carboxylic acid; adding if desired, other detergent actives and minor additives such as herein described to the soap mixture ; and converting the product of step (c) into bars by a known method.
- one or more detergent active precursors and the phosphorus containing mineral acid are reacted with an alkali to simultaneously form the neutralised active and the phosphate.
- the neutralised active is first formed by reacting one or more detergent active precursors with an alkali, followed by mixing the neutralised active with the phosphorus containing mineral acid and, if required, alkali to obtain the mixture of neutralised active and phosphate.
- a) the neutralised active is formed by reacting one or more detergent active precursors with an alkali and b) the phosphate is formed by reacting a phosphorus containing mineral acid with an alkali, and the neutralised active and phosphate so formed are mixed.
- the detergent active precursors comprise fatty acids and/or fat .
- the alkali used for soap formation can be any conventional alkali e.g. caustic soda, soda ash, caustic potash, sodium aluminate etc. More preferred alkalis include caustic soda and/or an aluminium containing alkali (e.g. sodium aluminate) . Sodium aluminate with a solid content of 20 to
- Preferred phosphorus containing mineral acids are orthophosphoric acid and sodium acid pyrophosphate (disodium dihydrogen pyrophosphate) .
- aluminium containing alkali When an aluminium containing alkali is used, it is especially preferable to maintain a weight ratio of aluminium oxide (AI 2 O 3 ) to phosphorus containing mineral acid in the range 0.40 to 2.40.
- the detergent bar of the invention has up to 5% free fatty acid.
- the free fatty acid can be added at any step during the process of soap making as described above. Alternatively, it can be generated in-situ by adding a suitable material that will break down the soap to generate free fatty acid. Examples of such materials include citric acid, adipic acid etc. The materials are preferably added after step (c) of the process described above.
- composition according to the invention will comprise one or more detergent actives which are generally chosen from anionic, nonionic, cationic, amphoteric or zwitterionic detergent actives.
- the detergent active is an anionic active, more preferably a soap.
- soap is meant neutralised total fatty matter.
- at least 75% of the detergent active is soap.
- total fatty matter usually abbreviated to TFM is used to denote the percentage by weight of fatty acid and triglyceride residues present without taking into account the accompanying cations.
- an accompanying sodium cation will generally amount to about 8% by weight.
- Other cations may be employed as desired, for example zinc, potassium, magnesium, alkyl ammonium and aluminium.
- soap denotes salts of carboxylic fatty acids.
- the soap may be derived from any of the triglycerides conventionally used in soap manufacture - consequently the carboxylate anions in the soap may contain from 8 to 22 carbon atoms .
- the soap may be obtained by saponifying a fat and/or a fatty acid.
- the fats or oils generally used in soap manufacture may be such as tallow, tallow stearines, palm oil, palm stearines, soya bean oil, fish oil, castor oil, rice bran oil, sunflower oil, coconut oil, babassu oil, palm kernel oil, and others.
- the fatty acids are derived from oils/fats selected from coconut, rice bran, groundnut, tallow, palm, palm kernel, cotton seed, soybean, castor etc.
- the fatty acid soaps can also be synthetically prepared (e.g. by the oxidation of petroleum or by the hydrogenation of carbon monoxide by the Fischer-Tropsch process) .
- Resin acids such as those present in tall oil, may be used. Naphthenic acids are also suitable.
- Tallow fatty acids can be derived from various animal sources and generally comprise about 1-8% myristic acid, about 21-32% palmitic acid, about 14-31% stearic acid, about 0-4% palmitoleic acid, about 36-50% oleic acid and about 0- 5% linoleic acid.
- a typical distribution is 2.5% myristic acid, 29% palmitic acid, 23% stearic acid, 2% palmitoleic acid, 41.5% oleic acid, and 3% linoleic acid.
- Other similar mixtures, such as those from palm oil and those derived from various animal tallow and lard are also included.
- coconut oil refers to fatty acid mixtures having an approximate carbon chain length distribution of 8% C8, 7% CIO, 48% C12, 17% C14, 8% C16, 2% C18, 7% oleic and 2% linoleic acids (the first six fatty acids listed being saturated) .
- Other sources having similar carbon chain length distributions, such as palm kernel oil and babassu kernel oil, are included within the term coconut oil .
- a typical suitable fatty acid blend consists of 5 to 30% coconut fatty acids and 70 to 95% fatty acids ex-hardened rice bran oil .
- Fatty acids derived from other suitable oils/fats such as groundnut, soybean, tallow, palm, palm kernel, etc. may also be used in other desired proportions.
- Suitable anionic detergent active compounds are water soluble salts of organic sulphuric reaction products having in the molecular structure an alkyl radical containing from 8 to 22 carbon atoms, and a radical chosen from sulphonic acid or sulphuric acid ester radicals and mixtures thereof.
- Suitable anionic detergents are sodium and potassium alcohol sulphates, especially those obtained by sulphating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; sodium and potassium alkyl benzene sulphonates such as those in which the alkyl group contains from 9 to 15 carbon atoms; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulphates; sodium and potassium salts of sulphuric acid esters of the reaction product of one mole of a higher fatty alcohol and from 1 to 6 moles of ethylene oxide; sodium and potassium salts of alkyl phenol ethylene oxide ether sulphate with from 1 to 8 units of ethylene oxide molecule and in which the alkyl radicals contain from 4 to 14 carbon atoms; the reaction product of fatty acids esterified with isethionic acid and neutralised with sodium hydroxide where, for example,
- the preferred water-soluble synthetic anionic detergent active compounds are the alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and magnesium) salts of higher alkyl benzene sulphonates and mixtures with olefin sulphonates and higher alkyl sulphates, and the higher fatty acid monoglyceride sulphates .
- Suitable nonionic detergent active compounds can be broadly described as compounds produced by the condensation of alkylene oxide groups, which are hydrophilic in nature, with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature. The length of the hydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
- Particular examples include the condensation product of aliphatic alcohols having from 8 to 22 carbon atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut oil ethylene oxide condensate having from 2 to 15 moles of ethylene oxide per mole of coconut alcohol; condensates of alkylphenols whose alkyl group contains from 6 to 12 carbon atoms with 5 to 25 moles of ethylene oxide per mole of alkylphenol ; condensates of the reaction product of ethylenediamine and propylene oxide with ethylene oxide, the condensate containing from 40 to 80% of polyoxyethylene radicals by weight and having a molecular weight of from 5,000 to 11,000; tertiary amine oxides of structure R 3 NO, where one group R is an alkyl group of 8 to 18 carbon atoms and the others are each methyl, ethyl or hydroxyethyl groups, for instance dimethyldodecylamine oxide; tertiary phosphine oxides of structure
- compositions according to the invention It is also possible to include cationic, amphoteric or zwitterionic detergent actives in the compositions according to the invention.
- Suitable cationic detergent actives that can be incorporated are alkyl substituted quaternary ammonium halide salts e.g. bis (hydrogenated tallow) dimethylammonium chlorides, cetyltrimethyl ammonium bromide, benzalkonium chlorides and dodecylmethylpolyoxyethylene ammonium chloride and amine and imidazoline salts for e.g. primary, secondary and tertiary amine hydrochlorides and imidazoline hydrochlorides .
- alkyl substituted quaternary ammonium halide salts e.g. bis (hydrogenated tallow) dimethylammonium chlorides, cetyltrimethyl ammonium bromide, benzalkonium chlorides and dodecylmethylpolyoxyethylene ammonium chloride and amine and imidazoline salts for e.g. primary, secondary and tertiary amine hydrochlorides and imidazoline hydrochlorides .
- Suitable amphoteric detergent-active compounds that optionally can be employed are derivatives of aliphatic secondary and tertiary amines containing an alkyl group of 8 to 18 carbon atoms and an aliphatic radical substituted by an anionic water-solubilizing group, for instance sodium 3- dodecylamino-propionate, sodium 3-dodecylaminopropane sulphonate and sodium N-2-hydroxydodecyl-N-methylta ⁇ rate .
- Suitable zwitterionic detergent-active compounds that optionally can be employed are derivatives of aliphatic quaternary ammonium, sulphonium and phosphonium compounds having an aliphatic radical of from 8 to 18 carbon atoms and an aliphatic radical substituted by an anionic water- solubilising group, for instance betaines such as 3-(N-N- dimethyl-N-hexadecylammonium) propane-1-sulphonate betaine, 3- (dodecylmethyl sulphonium) propane-1- sulphonate betaine and 3- (cetylmethylphosphonium) ethane sulphonate betaine.
- betaines such as 3-(N-N- dimethyl-N-hexadecylammonium) propane-1-sulphonate betaine, 3- (dodecylmethyl sulphonium) propane-1- sulphonate betaine and 3- (cetylmethylphosphonium) ethane sulphonate betaine
- the detergent bar of the invention essentially comprises one or more water soluble salts of organic carboxylic acids.
- Organic carboxylic acids suitable for the invention include C1-C10 carboxylic acids.
- Preferred salts include the alkali or alkaline earth metal salts of formic, acetic, propionic, citric, lactic and tartaric acid.
- Especially preferred salts are sodium and/or potassium formates, acetates, citrates, lactates and tartarates .
- Most preferred salts are chosen from sodium formate, sodium acette, sodium citrate, sodium lactate and sodium tartarate.
- moisturisers and humectants include polyols, glycerol, cetyl alcohol, Carbopol 934 (trade name), ethoxylated castor oil, paraffin oils, lanolin and its derivatives. Silicone compounds such as silicone surfactants like DC3225C (Dow Corning) and/or silicone emollients, or silicone oil (DC-200 Ex-Dow Corning) may also be included.
- Suitable sunscreens include 4-tertiary butyl- 4 ' -methoxy dibenzoylmethane (available under the trade name PARSOL 1789 from Givaudan) and/or 2-ethyl hexyl methoxy cinnamate (available under the trade name PARSOL MCX from Givaudan), or other UV-A and UV-B sunscreens.
- the preferred process of the invention comprises the steps of:
- step (c) converting the product of step (c) into bars by a known method.
- the mixture of phosphate and neutralised active can conveniently be obtained by any of the following methods: 1) generating the phosphate and the neutralised active consecutively (either the phosphate or the neutralised active can be generated first) 2) generating the neutralised active and phosphate simultaneously or 3) by generating the neutralised active and phosphate separately and then mixing the same .
- glycerine When an oil/fat is neutralised to generate the soap, glycerine is formed. In the process of the invention, the glycerine may be retained in the soap or may be removed.
- the water-soluble organic carboxylic acid may be added or generated prior to the neutralisation of the detergent active, or at any step after the neutralisation of the active .
- High shear kneading mixers suitable for the invention include ploughshare mixer, mixers with kneading members of Sigma type, multi-wiping overlap, single curve or double arm.
- the double arm kneading mixers can be of overlapping or the tangential design.
- the invention can be carried out in a helical screw agitator vessel or multi-head dosing pump/high shear mixer and spray drier combinations, as in conventional processing.
- a mixture of fatty acids at 80-85°C and alpha olefin sulphonate (AOS) were taken into a ploughshare mixture.
- the fatty acids were neutralised with an alkali solution.
- caustic soda was used for neutralisation
- Comparative Examples B-E and Examples 2-5 45% sodium aluminate solution was used.
- the present invention provides for synergistic phosphate structured detergent bars that show minimal or no efflorescence.
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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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/501,703 US7958791B2 (en) | 2002-01-22 | 2003-01-22 | Cryogenic storage device comprising a transponder |
AU2003208333A AU2003208333A1 (en) | 2002-02-13 | 2003-01-22 | Detergent bar and process of manufacture |
BR0307395-5A BR0307395A (pt) | 2002-02-13 | 2003-01-22 | Composição de barra de detergente e seu processo de preparação |
ZA2004/05186A ZA200405186B (en) | 2002-02-13 | 2004-06-29 | Detergent bar and process of manufacture |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN131/MUM/2002 | 2002-02-13 | ||
IN131MU2002 | 2002-02-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003068901A1 true WO2003068901A1 (fr) | 2003-08-21 |
Family
ID=27676889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2003/000625 WO2003068901A1 (fr) | 2002-01-22 | 2003-01-22 | Detergent en pain et son procede de fabrication |
Country Status (7)
Country | Link |
---|---|
CN (1) | CN1290991C (fr) |
AR (1) | AR038413A1 (fr) |
AU (1) | AU2003208333A1 (fr) |
BR (1) | BR0307395A (fr) |
MY (1) | MY148387A (fr) |
WO (1) | WO2003068901A1 (fr) |
ZA (1) | ZA200405186B (fr) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006061144A1 (fr) * | 2004-12-09 | 2006-06-15 | Unilever Plc | Procede de production d'une composition de pain presentant peu ou pas d'efflorescence |
WO2006138738A1 (fr) * | 2005-06-18 | 2006-12-28 | The Procter & Gamble Company | Composition de barre de nettoyage comprenant un niveau eleve d'eau |
WO2008070015A1 (fr) * | 2006-12-01 | 2008-06-12 | The Procter & Gamble Company | Compositions de barre de nettoyage comportant un niveau élevé d'eau |
WO2017202577A1 (fr) * | 2016-05-27 | 2017-11-30 | Unilever N.V. | Composition de nettoyage solide formée et son procédé de fabrication |
US11414632B2 (en) | 2019-03-01 | 2022-08-16 | Conopco, Inc. | Soap bar with improved perfume impact and deposition of actives |
US12006494B2 (en) | 2019-03-01 | 2024-06-11 | Conopco, Inc. | Bar compositions comprising C10 soap while minimizing ratio of unsaturated C18 soap to caprate |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3824189A (en) * | 1972-05-11 | 1974-07-16 | G Borello | Detergent compositions and methods for making same |
US4297230A (en) * | 1979-02-06 | 1981-10-27 | The Procter & Gamble Company | Non-crystallizing transparent soap bars |
GB2271120A (en) * | 1992-09-30 | 1994-04-06 | Unilever Plc | Shaped detergent composition comprising mutant subtilisin |
WO1998054285A1 (fr) * | 1997-05-30 | 1998-12-03 | The Procter & Gamble Company | Barre de lessive contenant une protease d'une plus grande stabilite |
WO1999050382A1 (fr) * | 1998-03-30 | 1999-10-07 | The Procter & Gamble Company | Compositions detergentes |
WO2001042414A1 (fr) * | 1999-12-08 | 2001-06-14 | Unilever Plc | Procede de preparation d'une composition de tablette de detergent |
US6310016B1 (en) * | 1999-12-08 | 2001-10-30 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Detergent bar composition and manufacturing process comprising colloidal aluminum hydroxide phosphate complex |
-
2003
- 2003-01-22 AU AU2003208333A patent/AU2003208333A1/en not_active Abandoned
- 2003-01-22 CN CNB038037955A patent/CN1290991C/zh not_active Expired - Fee Related
- 2003-01-22 WO PCT/EP2003/000625 patent/WO2003068901A1/fr not_active Application Discontinuation
- 2003-01-22 BR BR0307395-5A patent/BR0307395A/pt not_active Application Discontinuation
- 2003-02-11 MY MYPI20030461A patent/MY148387A/en unknown
- 2003-02-11 AR ARP030100418A patent/AR038413A1/es active IP Right Grant
-
2004
- 2004-06-29 ZA ZA2004/05186A patent/ZA200405186B/en unknown
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3824189A (en) * | 1972-05-11 | 1974-07-16 | G Borello | Detergent compositions and methods for making same |
US4297230A (en) * | 1979-02-06 | 1981-10-27 | The Procter & Gamble Company | Non-crystallizing transparent soap bars |
GB2271120A (en) * | 1992-09-30 | 1994-04-06 | Unilever Plc | Shaped detergent composition comprising mutant subtilisin |
WO1998054285A1 (fr) * | 1997-05-30 | 1998-12-03 | The Procter & Gamble Company | Barre de lessive contenant une protease d'une plus grande stabilite |
WO1999050382A1 (fr) * | 1998-03-30 | 1999-10-07 | The Procter & Gamble Company | Compositions detergentes |
WO2001042414A1 (fr) * | 1999-12-08 | 2001-06-14 | Unilever Plc | Procede de preparation d'une composition de tablette de detergent |
US6310016B1 (en) * | 1999-12-08 | 2001-10-30 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Detergent bar composition and manufacturing process comprising colloidal aluminum hydroxide phosphate complex |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006061144A1 (fr) * | 2004-12-09 | 2006-06-15 | Unilever Plc | Procede de production d'une composition de pain presentant peu ou pas d'efflorescence |
WO2006138738A1 (fr) * | 2005-06-18 | 2006-12-28 | The Procter & Gamble Company | Composition de barre de nettoyage comprenant un niveau eleve d'eau |
JP2008543882A (ja) * | 2005-06-18 | 2008-12-04 | ザ プロクター アンド ギャンブル カンパニー | 高濃度の水を含むクレンジングバー組成物 |
US8080503B2 (en) | 2005-06-18 | 2011-12-20 | The Procter & Gamble Company | Cleansing bar compositions comprising a high level of water |
WO2008070015A1 (fr) * | 2006-12-01 | 2008-06-12 | The Procter & Gamble Company | Compositions de barre de nettoyage comportant un niveau élevé d'eau |
WO2017202577A1 (fr) * | 2016-05-27 | 2017-11-30 | Unilever N.V. | Composition de nettoyage solide formée et son procédé de fabrication |
US11414632B2 (en) | 2019-03-01 | 2022-08-16 | Conopco, Inc. | Soap bar with improved perfume impact and deposition of actives |
US12006494B2 (en) | 2019-03-01 | 2024-06-11 | Conopco, Inc. | Bar compositions comprising C10 soap while minimizing ratio of unsaturated C18 soap to caprate |
Also Published As
Publication number | Publication date |
---|---|
AU2003208333A1 (en) | 2003-09-04 |
MY148387A (en) | 2013-04-15 |
CN1633494A (zh) | 2005-06-29 |
BR0307395A (pt) | 2004-11-09 |
CN1290991C (zh) | 2006-12-20 |
AR038413A1 (es) | 2005-01-12 |
ZA200405186B (en) | 2005-08-31 |
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