WO2000000577A2 - Rinse conditioner composition - Google Patents
Rinse conditioner composition Download PDFInfo
- Publication number
- WO2000000577A2 WO2000000577A2 PCT/EP1999/004153 EP9904153W WO0000577A2 WO 2000000577 A2 WO2000000577 A2 WO 2000000577A2 EP 9904153 W EP9904153 W EP 9904153W WO 0000577 A2 WO0000577 A2 WO 0000577A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- care active
- composition
- colour care
- laundry
- fabric
- 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.)
- Ceased
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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
Definitions
- the present invention relates to rinse conditioner compositions.
- the present invention relates to rinse conditioner compositions that give an additional benefit, other than merely softening or perfuming the fabric, particularly preventing colour fading of fabrics.
- Rinse conditioners are commonly used to deposit a softening compound and a perfume onto a fabric. Their use to deposit other fabric treatment aids has been commercially limited mainly due to difficulties in depositing the fabric treatment aid onto a fabric .
- US 4 788 054 (Bernhardt) teaches the use of N- phenylphthalisomides as ultraviolet radiation absorbers for cotton, wool, polyester and rayon.
- the compositions require that an aqueous sulphuric acid vehicle is required for deposition.
- US 5474691 Severns teaches that photofading of fabrics can be prevented by treating the fabric using a tumble dryer article comprising a conditioning compound, a uv absorbers and/or an antioxidant.
- this system of delivering the uv absorber/antioxidant to the laundry results in an uneven deposition of uv absorber/antioxidant.
- a further disadvantage with this system is that a high level of uv absorber/antioxidant has to be used.
- WO 96/03486 discloses fabric care compositions to reduce the fading of fabrics from sunlight, comprising a light stable sunscreen compound.
- the problems associated with the prior art of poor deposition and thus use of high levels of Colour Care Active are addressed by the present invention.
- the present invention also addresses the problems of incompatibility between the softening compound and a Colour Care Active and the problem of poor phase stability of the rinse conditioner.
- a rinse conditioner comprising a cationic fabric softening compound and 0.01% to 10% by weight of the total composition of a Colour Care Active, wherein the Colour Care Active is not light stable and further wherein when the composition comprises 0.05 wt% or less of the Colour Care Active the cationic fabric softening compound comprises a quaternary ammonium compound having at least one ester linking group or nonionic fabric softening compounds, or mixtures thereof .
- the invention also provides a process for treating laundry, the process having the following steps:
- the invention further provides the use rinse conditioner composition according to the invention prevent the fading of coloured fabrics.
- the present invention has the advantage that it delivers a Colour Care Active onto the fabric with very little Colour Care Active being wasted within the rinse liquor.
- compositions of the invention have the further advantage that the Fabric Treatment Aid is not incompatible with the fabric softening phase of the formulation and thus there is little, or no, phase instability.
- the sunscreen agents of the present invention demonstrate light stability in the compositions of the present invention.
- Light stable means that the sunscreen compounds in the compositions of the present invention do not decompose when exposed to either sunlight or simulated sunlight for approximately 2 to 60 hours at a temperature of from about 25°C to about 45°C.
- the Colour Care Active used according to the invention is any compound, not stable to light, used to give an effect other than the commonplace effects of cleaning, softening or perfuming the fabrics .
- Colour Care Actives include compounds used to prevent the fading of coloured fabrics.
- the invention also encompasses mixtures of these agents. This invention is particularly advantageous in delivering compounds used to prevent the fading of coloured fabrics, which may be mixtures of UV absorbers .
- Colour Care Active in the context of the present application specifically excludes perfumes, strongly ionising species such as cationic quaternary ammonium compounds, sulphonates, phosphates and polymeric compounds.
- the term includes fabric anti- fading agents (including UV absorbing compounds) .
- the Colour Care Active is preferably hydrophobic as these materials deposit well onto the fabric in the presence of the delivery system of the present invention.
- the term not light stable refers to those agents which degrade with time when exposed to UV radiation, in particular to those showing average degradation values of approximately 25% or greater, over a period of 5 hours .
- the Colour Care Active is present in the compositions at a level from 0.01 to 10 % by weight of the total composition.
- the cationic fabric softening composition comprises a quaternary ammonium compound having at least one ester linking group, or a nonionic fabric softening compound or mixtures thereof.
- compositions comprise from 0.025 to 9 % by weight of the Colour Care Active more preferably more than 0.5 to 8.5%, e.g. 0.55 to 7 %. Often amounts less than 5% may be used.
- the level of Colour Care Active to be used in a given composition is dependent on the Agent that is to be delivered.
- the ratio of Colour Care Active to cationic softening compound is preferably from 4:1 to 1:500, more preferably from 1:180 to 1:7.
- the Colour Care agent is preferably non fabric staining. It may be a single UV absorbing compound or a mixture of compounds which absorb solar radiation in the wavelength range280nm through to 400nm. More preferable are those UV absorber compounds which have high extinction coefficients across this part of the spectrum.
- UV absorbers examples include the following. This list is not meant to be exclusive:
- UV absorbers for use in the present invention are:
- 2-ethylhexyl-4-methoxycinnamate also known as 2-ethylhexyl- 3- (4-methoxyphenyl) propenoate (PARSOL MCX ex Givaudan) ;
- the fabric care agent preferably has a c.logP. of value of 4.0 or more, preferably 5.0 or more, more preferably 5.2 or more.
- any suitable fabric softening compound is suitable for use with the present invention, in particular nonionic softening compounds and cationic softening compounds .
- the compositions of the inventions comprise the Colour Care Active in an amount of up to 0.05% at most
- the cationic fabric softening compound in this case comprises a quaternary ammonium compound having at least one ester linking group or nonionic fabric softening compounds, or mixtures therefore.
- the fabric softening compound may comprise any fabric softening compound as referred to herein.
- the fabric softening compound is cationic in nature.
- the cationic fabric softening compound of the invention has two long chain alkyl or alkenyl chains with an average chain length greater than Ci 4 , more preferably each chain has an average chain length greater than C 16 , more preferably at least 50% of each long chain alkyl or alkenyl group has a chain length of C ⁇ g ⁇
- the long chain alkyl or alkenyl groups of the fabric softening compound are predominantly linear.
- the cationic fabric softening compositions of the invention are compounds which provide excellent softening, characterised by chain melting -L ⁇ to L ⁇ - transition temperature greater than 25°C, preferably greater than 35°C, most preferably greater than 45°C.
- This L ⁇ to L ⁇ transition can be measured by DSC as defined in "Handbook of Lipid Bilayers, D Marsh, CRC Press, Boca Raton Florida, 1990 (Pages 137 and 337) .
- the softening compound is substantially insoluble in water.
- substantially insoluble fabric softening compounds in the context of this invention are defined as fabric softening compounds having a solubility less than 1 x 10 Wt% in demineralised water at 20°C, preferably the fabric softening compounds have a solubility
- the fabric softening compounds have a solubility at 20°C in demineralised water from 1 x 10 "8 to 1 x l ⁇ "6-
- the fabric softening compound is quaternary ammonium compound, especially a water insoluble quaternary ammonium material which comprises a compound having two C 12 - 18 alkyl or alkenyl groups connected to the molecule via at least one an ester link.
- This is an ester linking group as referred to above. It is more preferred if the quaternary ammonium material has two ester links present.
- the especially preferred ester-linked quaternary ammonium material for use in the invention can be represented by the formula:
- each R group is independently selected from ⁇ . 4 alkyl, hydroxyalkyl or C 2 - 4 alkenyl groups; and wherein each 2 R group is independently selected from C 8 _ 28 alkyl or alkenyl groups ;
- T is -O-C- or -C-0-;
- X is any suitable anion and n is an integer from 0-5.
- a second preferred type of quaternary ammonium material can be represented by the formula:
- R lr X n and R 2 are as defined above.
- the quaternary ammonium material is biologically degradable .
- Preferred materials of this class such as 1,2 bis [hardened tallowoyloxy] -3-trimethylammonium propane chloride and their method of preparation are, for example, described in US 4 137 180 (Lever Brothers) .
- these materials comprise small amounts of the corresponding monoester as described in US 4 137 180 for example di-hardened tallowoyloxy -2-hydroxy trimethylammonium propane chloride.
- the fabric softening agent may also be polyol ester quats (PEQs) as described in EP 0638 639 (Akzo) .
- Suitable nonionic softening agents include pentaerythritol esters, sorbitan esters, mono, di and triglycerides.
- compositions typically comprise 0.1-50% by weight of the fabric softening agent, preferably 1-45%. If the compositions are concentrated compositions they preferably comprise 8%-50% by weight fabric softener, e.g. 8%-35%. If the compositions are dilute compositions they typically comprise 0.5-8% by weight fabric softener, e.g. 1-6%. Preferably the compositions are free of sulphuric acid.
- compositions of the invention preferably have a pH of at least 1.5, preferably 1.5 to 5.
- the composition can also contain fatty acids, for example C 8 -C 24 alkyl or alkenyl monocarboxylic acids, or polymeric carboxylic acids.
- fatty acids for example C 8 -C 24 alkyl or alkenyl monocarboxylic acids, or polymeric carboxylic acids.
- saturated fatty acids are used, in particular, hardened tallow C ⁇ -Ci ⁇ fatty acids.
- the level of fatty acid material is preferably more than 0.1% by weight, more preferably more than 0.2% by weight. Especially preferred are concentrates comprising from 0.5 to 20% by weight of fatty acid, more preferably 1% to 10% by weight.
- the weight ratio of fabric softening compound to fatty acid material is preferably from 10:1 to 1:10.
- the composition can also contain one or more optional ingredients, selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, colourants, hydrotropes, antifoaming agents, polymeric or other thickening agents, opacifiers, antioxidants and anti- corrosion agents.
- compositions of the invention may be in any product form such as solid (e.g. powder or granules) or a paste; however it is preferred if they are liquid.
- the principal medium for the composition will often be water, although compositions may comprise up to 10 wt% of a water-miscible solvent .
- compositions of the invention do not contain alkoxylated ⁇ -sitosterol compounds.
- a process for treating laundry using the above compositions typically comprises the steps as below:
- washing vessel for example a bucket. Any suitable vessel may be used.
- the following rinse conditioner products were prepared using a Silverson high shear mixer. Sunscreen was incorporated into hot water, without pre-heating, after addition of the molten active.
- Givaudan It is unstable to light and has a clogP value of 5.2.
- Example 1 is a dilute rinse conditioner whilst examples 2 and 3 are concentrated rinse conditioners.
- Parsol MCX Parsol MCX.
- the control for the example 1 contained 4.8 wt%
- examples 2 and 3 contained 24.2 wt% fabric softener and the same amount of minors, with water to make the composition to 100%.
- Example 1 and its control were tested in a Miele front loading washing machine (10 litre fill) @ 40°C, 12° FH water. There were 4 cold rinse, 12° FH, (23 litre fill) .
- Example 1 and its control were washed in Persil Automatic colour variant purchased in UK, 75 g/wash.
- Example 1 125 g in the final rinse.
- Examples 2 and 3 30 ml in the final rinse.
- Example 1 - 24 approx, 1 m pieces of de-sized 65:35 polyester: cotton sheeting fabric made into 6 overlooked multilayer sandwiches 4 cloths thick, plus
- Example 1 4 pieces of cotton sheeting 50 x 50 cm each with 10 x 10 cm test pieces attached as; 4 pieces dyed fabric in corners, 2 pieces of white fabric in centre.
- each test monitor was taken using an ICS spectroflash 500 reflectometer . Each cloth is measured in 2 positions on the side that bears the label and which has been irridated.
- the reflectomer software is used to calculate Delta E values according to the CIELAB 1964 supplement for D65 illuminant and 10 c observer .
- the cloths were attached to ballast pieces.
- the test cloths for example 1 were added, evenly distributed to the drum and the washing powder and rinse conditioner added to the dispensing draw.
- test cloths for example 2 and 3 were added to the machine which was approx % full of water and to which the washing powder had been added and had dispersed.
- the cloths were added as the water fill completed. 3.
- the washing cycles were completed with the compositions of examples 2 and 3 being added during the rinse fill and being dispersed in the water and not added directly onto the cloths.
- ⁇ E is the colour difference between the average values of control and sample .
- the measured cloths were exposed in an Atlas Weatherometer Weatherometer model Ci65 ex Atlas Electric Devices of Chicago that mimics Florida sunshine to 1 hour of simulated Florida midday sunlight. The cloths were measured again and then exposed again and re-measured until the cloths had been irradiated for 5 hours and the cloths measured five times.
- the degradation can be calculated by 100- the % remaining on the fabric.
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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)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU46112/99A AU4611299A (en) | 1998-06-29 | 1999-06-16 | Rinse conditioner composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9814074.2A GB9814074D0 (en) | 1998-06-29 | 1998-06-29 | Fabric softener composition |
| GB9814074.2 | 1998-06-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2000000577A2 true WO2000000577A2 (en) | 2000-01-06 |
| WO2000000577A3 WO2000000577A3 (en) | 2001-08-16 |
Family
ID=10834621
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1999/004153 Ceased WO2000000577A2 (en) | 1998-06-29 | 1999-06-16 | Rinse conditioner composition |
Country Status (5)
| Country | Link |
|---|---|
| AR (1) | AR019706A1 (en) |
| AU (1) | AU4611299A (en) |
| BR (1) | BR9803130C1 (en) |
| GB (1) | GB9814074D0 (en) |
| WO (1) | WO2000000577A2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6946501B2 (en) | 2001-01-31 | 2005-09-20 | The Procter & Gamble Company | Rapidly dissolvable polymer films and articles made therefrom |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1158634A (en) * | 1994-07-26 | 1997-09-03 | 普罗格特-甘布尔公司 | Rinse added fabric softener compsns. containing sunscreens for sunfade protection for fabrics |
| US5500138A (en) * | 1994-10-20 | 1996-03-19 | The Procter & Gamble Company | Fabric softener compositions with improved environmental impact |
| CA2254855C (en) * | 1996-05-23 | 2006-11-28 | Unilever Plc | Fabric conditioning composition |
-
1998
- 1998-06-29 GB GBGB9814074.2A patent/GB9814074D0/en not_active Ceased
- 1998-08-10 BR BR9803130A patent/BR9803130C1/en not_active IP Right Cessation
-
1999
- 1999-06-16 AU AU46112/99A patent/AU4611299A/en not_active Abandoned
- 1999-06-16 WO PCT/EP1999/004153 patent/WO2000000577A2/en not_active Ceased
- 1999-06-24 AR ARP990103030 patent/AR019706A1/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6946501B2 (en) | 2001-01-31 | 2005-09-20 | The Procter & Gamble Company | Rapidly dissolvable polymer films and articles made therefrom |
| US7547737B2 (en) | 2001-01-31 | 2009-06-16 | The Procter & Gamble Company | Rapidly dissolvable polymer films and articles made therefrom |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000000577A3 (en) | 2001-08-16 |
| BR9803130A (en) | 2000-01-18 |
| GB9814074D0 (en) | 1998-08-26 |
| AU4611299A (en) | 2000-01-17 |
| BR9803130C1 (en) | 2000-06-13 |
| AR019706A1 (en) | 2002-03-13 |
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