CA2078717C - Fragrance microcapsules for fabric conditioning - Google Patents
Fragrance microcapsules for fabric conditioningInfo
- Publication number
- CA2078717C CA2078717C CA002078717A CA2078717A CA2078717C CA 2078717 C CA2078717 C CA 2078717C CA 002078717 A CA002078717 A CA 002078717A CA 2078717 A CA2078717 A CA 2078717A CA 2078717 C CA2078717 C CA 2078717C
- Authority
- CA
- Canada
- Prior art keywords
- wax
- emulsifiable
- microcapsules
- perfume
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/047—Arrangements specially adapted for dry cleaning or laundry dryer related applications
-
- 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
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
-
- 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
Abstract
Composite microcapsules and a method of making the microcapsules, as well as a tumble drier article incorporating the microcapsules are described. The microcapsules comprise particles made of a emulsifiable mixture of a wax material and a fragrance oil which are embedded in a water soluble polymer. The microcapsules have a diameter of less than about 100 microns and are useful for incorporation in tumble drier articles to control the release of fragrance in the drier and prevent loss of fragrance during processing and storage.
Description
2 07 ~7 ~
FRAGRANCE MICROCAPSULES FOR FABRIC CONDITIONING
1. Field of the Invention This invention relates to a water soluble polymer which encapsulates particles made of an emulsifiable mixture of a fragrance and a wax to form microcapsules which are used to improve the deposition of fragrance onto fabrics.
2. Backqround of the Invention The use of fragrance to provide a pleasing scent to freshly dried fabrics, as well as to modify or enhance the fragrance of fabric conditioning articles, is both desirable and well known in the art as illustrated in U.S.
4,954,285 issued to Wierenga et al. However, the efficient deposition of such perfumes on fabrics as well as the manufacturing of fabric conditioning articles has not been achieved to date. The volatile perfumes tend to be lost during manufacturing of the tumble drier sheets as well as during their storage and use by the consumer.
Various techniques have been tried in the prior art to address these problems. In general, these techniques ~ 207g~
involve entrapping the volatile fragrance oil with a coating or mixing the oil with a suitable carrier.
Solid fragrance particles have also been prepared by mixing and absorbing the fragrance oil with a solid carrier to deliver fragrance to a product.
In U.S. 4,152,272 particles are formed from a perfume/wax mixture. The resulting particles are primarily incorporated into an aqueous fabric conditioner composition. This type of perfume/wax particle is undesirable for the manufacture of such particles into a tumble drier sheet because the molten fabric softener actives deposited on the sheets reach temperatures of up to 80~C. Such manufacturing temperatures would cause the majority of the perfume containing particles with melting points below the processing temperature to melt, releasing the majority of the fragrance during manufacturing of the sheets rather than being deposited on the drying fabrics.
For those wax/perfume particles having melting points above the processing temperature the perfume is extracted by the molten active softener material.
In U.S. 4,954,285: 4,536,315 and 4,073,996 perfumed oils are mixed and absorbed with an inorganic carrier such as clay or silica to deliver perfume in detergents and fabric softeners. In U.S. 4,326,967 and EP 334,666 perfumes are emulsified in a wax or solid surfactant and the fragrance oil is released during heat treatment such as in a drier.
A fragrance containing polymer incorporated in detergent compositions comprising a water soluble polymer, a water insoluble polymer and a perfume composition which is part of both the water soluble and water insoluble polymers is described in U.S. 4,842,761. The two polymers are 2~7~7~
FRAGRANCE MICROCAPSULES FOR FABRIC CONDITIONING
1. Field of the Invention This invention relates to a water soluble polymer which encapsulates particles made of an emulsifiable mixture of a fragrance and a wax to form microcapsules which are used to improve the deposition of fragrance onto fabrics.
2. Backqround of the Invention The use of fragrance to provide a pleasing scent to freshly dried fabrics, as well as to modify or enhance the fragrance of fabric conditioning articles, is both desirable and well known in the art as illustrated in U.S.
4,954,285 issued to Wierenga et al. However, the efficient deposition of such perfumes on fabrics as well as the manufacturing of fabric conditioning articles has not been achieved to date. The volatile perfumes tend to be lost during manufacturing of the tumble drier sheets as well as during their storage and use by the consumer.
Various techniques have been tried in the prior art to address these problems. In general, these techniques ~ 207g~
involve entrapping the volatile fragrance oil with a coating or mixing the oil with a suitable carrier.
Solid fragrance particles have also been prepared by mixing and absorbing the fragrance oil with a solid carrier to deliver fragrance to a product.
In U.S. 4,152,272 particles are formed from a perfume/wax mixture. The resulting particles are primarily incorporated into an aqueous fabric conditioner composition. This type of perfume/wax particle is undesirable for the manufacture of such particles into a tumble drier sheet because the molten fabric softener actives deposited on the sheets reach temperatures of up to 80~C. Such manufacturing temperatures would cause the majority of the perfume containing particles with melting points below the processing temperature to melt, releasing the majority of the fragrance during manufacturing of the sheets rather than being deposited on the drying fabrics.
For those wax/perfume particles having melting points above the processing temperature the perfume is extracted by the molten active softener material.
In U.S. 4,954,285: 4,536,315 and 4,073,996 perfumed oils are mixed and absorbed with an inorganic carrier such as clay or silica to deliver perfume in detergents and fabric softeners. In U.S. 4,326,967 and EP 334,666 perfumes are emulsified in a wax or solid surfactant and the fragrance oil is released during heat treatment such as in a drier.
A fragrance containing polymer incorporated in detergent compositions comprising a water soluble polymer, a water insoluble polymer and a perfume composition which is part of both the water soluble and water insoluble polymers is described in U.S. 4,842,761. The two polymers are 2~7~7~
physically associated with each other so that one polymer forms discreet entities in the matrix of the other polymer.
In general, although these free flowing solid particles provide for the controlled release oL the fragrance oil, the fragrance oil is generally not sufficiently protected so that it is frequently lost or destabilised during processing. It is also difficult to extract the fragrance when desired during use.
In U.S. 4,842,761 the perfume capsules largely depend on increasing size to increase the amount deposited on clothes or fabrics and compensate for perfume lost during processing. Additionally, the particles require a large amount of water (e.g. wash or rinse liquor) to release the fragrance oils. Thus, the polymer matrix of the '761 patent would not effectively deliver fragrance at the end of the drying cycle.
Water dispersible polymers have been used to encapsulate fragrance oils in conventional spray drying processes as described in U.S. 4,276,312; 3,971,852; 3,821,436;
3,758,223; 3,455,838; 3,159,585 and 3,091,567. Such solid particles are made by emulsifying fragrance oils into an aqueous solution of the water dispersible polymer such as gum arabic, starch or gelatin. The emulsion is then sprayed into a column of hot air to yield free flowing microcapsules with the oil entrapped or encapsulated inside the water soluble polymer. Such spray drying techniques have been widely employed to make encapsulated fragrance particles. However, the conventional processes are not suitable for manufacturing the claimed composite microcapsule because large aggregates of perfume wax mixture are formed which cannot be spray dried.
207~7~7 It is thus an object of the invention to provide fragrance encapsulated particles which will prevent the release and loss of the ma~ority of the fragrance oil during processing, storage and use of fabric conditioning articles and which will release the majority of the fragrance onto drying fabrics.
Additionally, the fragrance particles may be incorporated in a fabric softening composition and applied to a dispensing means to produce an article for use in automatic clothes dryers to condition fabrics.
Another object of the invention is to provide a novel process for forming the claimed microcapsules to avoid loss of fragrance oils during processing, storage and use.
2~7~717 SUMMARY OF THE INVENTION
The invention relates to composite microcapsules comprising a water soluble polymer encapsulating individual core particles formed from an emulsifiable mixture of wax and perfume. The emulsifiable mixture has a melting point of less than 100~C, preferably 35~C-90~C
and most preferably from 45~C to 85~C. The emulsifiable mixture should be emulsifiable in an aqueous solution to form core particles with a diameter of less than 5 micrometers and preferably less than 1 micrometer. The diameter of the microcapsules is no greater than 100 microns and preEerably less than about 40 microns.
The emulsifiable mixture may optionally be combined with a surfactant. The microcapsules are prepared by forming an emulsion of the emulsifiable mixture and the water soluble polymer then spray drying the emulsion to form the microcapsules. The microcapsules may be coated onto a dispensing means for release onto fabrics in an automatic clothes drier. In such an application, moisture from the washed fabrics at least partially dissolves the water soluble polymer and the perfume diffuses out of the microcapsules or the released core particles.
Temperatures of the drying cycle in the clothes drier may accelerate the release of the perfume by melting the wax of the core materials.
The wax materials which may be used to form the emulsifiable mixture in the invention include hydrocarbons such as paraffin wax and microcrystalline wax. Surfactant materials which may be used may be either cationic, anionic or nonionic surfactants such as an ethoxylated primary alcohol nonionic surfactant derived from C,6, C30, C40 and Cso average carbon chain length primary alcohols; a ~ 7~7 ~ ~
In general, although these free flowing solid particles provide for the controlled release oL the fragrance oil, the fragrance oil is generally not sufficiently protected so that it is frequently lost or destabilised during processing. It is also difficult to extract the fragrance when desired during use.
In U.S. 4,842,761 the perfume capsules largely depend on increasing size to increase the amount deposited on clothes or fabrics and compensate for perfume lost during processing. Additionally, the particles require a large amount of water (e.g. wash or rinse liquor) to release the fragrance oils. Thus, the polymer matrix of the '761 patent would not effectively deliver fragrance at the end of the drying cycle.
Water dispersible polymers have been used to encapsulate fragrance oils in conventional spray drying processes as described in U.S. 4,276,312; 3,971,852; 3,821,436;
3,758,223; 3,455,838; 3,159,585 and 3,091,567. Such solid particles are made by emulsifying fragrance oils into an aqueous solution of the water dispersible polymer such as gum arabic, starch or gelatin. The emulsion is then sprayed into a column of hot air to yield free flowing microcapsules with the oil entrapped or encapsulated inside the water soluble polymer. Such spray drying techniques have been widely employed to make encapsulated fragrance particles. However, the conventional processes are not suitable for manufacturing the claimed composite microcapsule because large aggregates of perfume wax mixture are formed which cannot be spray dried.
207~7~7 It is thus an object of the invention to provide fragrance encapsulated particles which will prevent the release and loss of the ma~ority of the fragrance oil during processing, storage and use of fabric conditioning articles and which will release the majority of the fragrance onto drying fabrics.
Additionally, the fragrance particles may be incorporated in a fabric softening composition and applied to a dispensing means to produce an article for use in automatic clothes dryers to condition fabrics.
Another object of the invention is to provide a novel process for forming the claimed microcapsules to avoid loss of fragrance oils during processing, storage and use.
2~7~717 SUMMARY OF THE INVENTION
The invention relates to composite microcapsules comprising a water soluble polymer encapsulating individual core particles formed from an emulsifiable mixture of wax and perfume. The emulsifiable mixture has a melting point of less than 100~C, preferably 35~C-90~C
and most preferably from 45~C to 85~C. The emulsifiable mixture should be emulsifiable in an aqueous solution to form core particles with a diameter of less than 5 micrometers and preferably less than 1 micrometer. The diameter of the microcapsules is no greater than 100 microns and preEerably less than about 40 microns.
The emulsifiable mixture may optionally be combined with a surfactant. The microcapsules are prepared by forming an emulsion of the emulsifiable mixture and the water soluble polymer then spray drying the emulsion to form the microcapsules. The microcapsules may be coated onto a dispensing means for release onto fabrics in an automatic clothes drier. In such an application, moisture from the washed fabrics at least partially dissolves the water soluble polymer and the perfume diffuses out of the microcapsules or the released core particles.
Temperatures of the drying cycle in the clothes drier may accelerate the release of the perfume by melting the wax of the core materials.
The wax materials which may be used to form the emulsifiable mixture in the invention include hydrocarbons such as paraffin wax and microcrystalline wax. Surfactant materials which may be used may be either cationic, anionic or nonionic surfactants such as an ethoxylated primary alcohol nonionic surfactant derived from C,6, C30, C40 and Cso average carbon chain length primary alcohols; a ~ 7~7 ~ ~
fabric softening component; or alkyl sulphonate.
Preferred surfactant materials are an ethoxylated primary alcohol and a cationic fabric softening compound, such as a quaternary ammonium compound.
Suitable water soluble polymers for use in the invention include synthetic polymers and natural or modified natural polymers with molecular weights of less than 100,000. In accordance with a specific aspect of the invention there is provided a tumble drier article of manufacture adapted for conditioning fabric in an automatic clothes .
drler comprlsmg:
(a) a fabric softening composition comprising a fabric softener selected from the group consisting of: cationic quaternary ammonium salts, tertiary fatty amines having at least one C8 to C30, alkyl groups, carboxylic acids having 8 to 30 carbon atoms and one carboxy group per molecule, esters of polyhydric alcohols, fatty alcohols, ethoxylated fatty alcohols, alkyl phenols, ethoxylated alkyl phenols, ethoxylated fatty amines, ethoxylated monoglycerides, ethoxylated diglycerides, mineral oils, polyols and mixtures thereof;
(b) between 0.5 and 80% by weight of spray dried composite microcapsules having a diameter less than 100 micrometers, each microcapsule material comprising individual particles of an emulsifiable mixture of wax material and a perfume composition, the mixture having a melting point between 35 and 90~C and a water soluble polymer wherein the wax material and the perfume composition are dispersed in the water soluble ~ ~ 7 polymer, and the individual particles of the mixture of wax and perfume composition having an average diameter of less than 5 micrometers;
5 (c) dispensing means for releasing the fabric softening composition and the microcapsules onto fabrics, the fabric softening composition being releasably attached to the dispensing means in a weight ratio of from 10:1 to 0.5:1 of the fabric softening composition to the dispensing means.
A further aspect of the invention provides a composite microcapsule containing a fragrance oil comprising:
(a) particles composed of an emulsifiable mixture of a self-emulsifiable wax material and optionally, a non-self-emulsifiable wax material, and a perfume composition, the mixture having a melting point between 35 and 90~C, the ratio of self-emulsifiable to non-self-emulsifiable wax being at least 1:3, the particles having an average diameter of less than 5 micrometers; and (b) a water soluble polymer encapsulating the particles to form composite microcapsules having a diameter less than 100 micrometers whereby the fragrance oil is released by dissolving the polymer upon contact with a liquid and melting the wax material at a temperature below 90~C, the microcapsules having been formed by a spray drying process.
A process for making a composite microcapsule of the form defined above is also provided.
.~
2~ ~7 1 ~
Preferred surfactant materials are an ethoxylated primary alcohol and a cationic fabric softening compound, such as a quaternary ammonium compound.
Suitable water soluble polymers for use in the invention include synthetic polymers and natural or modified natural polymers with molecular weights of less than 100,000. In accordance with a specific aspect of the invention there is provided a tumble drier article of manufacture adapted for conditioning fabric in an automatic clothes .
drler comprlsmg:
(a) a fabric softening composition comprising a fabric softener selected from the group consisting of: cationic quaternary ammonium salts, tertiary fatty amines having at least one C8 to C30, alkyl groups, carboxylic acids having 8 to 30 carbon atoms and one carboxy group per molecule, esters of polyhydric alcohols, fatty alcohols, ethoxylated fatty alcohols, alkyl phenols, ethoxylated alkyl phenols, ethoxylated fatty amines, ethoxylated monoglycerides, ethoxylated diglycerides, mineral oils, polyols and mixtures thereof;
(b) between 0.5 and 80% by weight of spray dried composite microcapsules having a diameter less than 100 micrometers, each microcapsule material comprising individual particles of an emulsifiable mixture of wax material and a perfume composition, the mixture having a melting point between 35 and 90~C and a water soluble polymer wherein the wax material and the perfume composition are dispersed in the water soluble ~ ~ 7 polymer, and the individual particles of the mixture of wax and perfume composition having an average diameter of less than 5 micrometers;
5 (c) dispensing means for releasing the fabric softening composition and the microcapsules onto fabrics, the fabric softening composition being releasably attached to the dispensing means in a weight ratio of from 10:1 to 0.5:1 of the fabric softening composition to the dispensing means.
A further aspect of the invention provides a composite microcapsule containing a fragrance oil comprising:
(a) particles composed of an emulsifiable mixture of a self-emulsifiable wax material and optionally, a non-self-emulsifiable wax material, and a perfume composition, the mixture having a melting point between 35 and 90~C, the ratio of self-emulsifiable to non-self-emulsifiable wax being at least 1:3, the particles having an average diameter of less than 5 micrometers; and (b) a water soluble polymer encapsulating the particles to form composite microcapsules having a diameter less than 100 micrometers whereby the fragrance oil is released by dissolving the polymer upon contact with a liquid and melting the wax material at a temperature below 90~C, the microcapsules having been formed by a spray drying process.
A process for making a composite microcapsule of the form defined above is also provided.
.~
2~ ~7 1 ~
Detailed DescriPtion of Preferred Embodiments of the ComPosites Microcapsules ;
The composite microcapsules of the invention may be added to tumble drier articles to provide eventual release of perfume compositions onto fabrics. The microcapsules are composed of small particles of an emulsifiable mixture of a wax and perfume composition optionally combined with a surfactant. The particles are individually embedded in a water soluble polymer matrix. Thus multiple release modes are used to deposit the perfume fragrance onto fabrics.
Specifically the polymer matrix dissolves, partially or completely, upon contact with wet fabrics and the perfume of the particles diffuses out. Diffusion is accelerated by melting the wax of the particles. The microcapsules may be incorporated in a tumble articles to releasably control the deposition of the perfume fragrance onto fabrics during drying.
The water soluble polymer matrix of the microcapsules at least partially dissolves upon contact with washed fabrics from a washing cycle. Perfume then may diffuse from released particles or from particles still within the partially dissolved polymer material.
The emulsifiable material has a melting point defined as the highest transition temperature above the point where the emulsifiable mixture becomes a flowable liquid, as measured by a conventional Differential Scanning Calorimeter. The core materials should be emulsifiable in an aqueous solution. The melting point of the particles is less than about 100~C, preferably about 35~C to about 90~C and most preferably from about 45~C to about 85~C.
2 0 ~
The composite microcapsules of the invention may be added to tumble drier articles to provide eventual release of perfume compositions onto fabrics. The microcapsules are composed of small particles of an emulsifiable mixture of a wax and perfume composition optionally combined with a surfactant. The particles are individually embedded in a water soluble polymer matrix. Thus multiple release modes are used to deposit the perfume fragrance onto fabrics.
Specifically the polymer matrix dissolves, partially or completely, upon contact with wet fabrics and the perfume of the particles diffuses out. Diffusion is accelerated by melting the wax of the particles. The microcapsules may be incorporated in a tumble articles to releasably control the deposition of the perfume fragrance onto fabrics during drying.
The water soluble polymer matrix of the microcapsules at least partially dissolves upon contact with washed fabrics from a washing cycle. Perfume then may diffuse from released particles or from particles still within the partially dissolved polymer material.
The emulsifiable material has a melting point defined as the highest transition temperature above the point where the emulsifiable mixture becomes a flowable liquid, as measured by a conventional Differential Scanning Calorimeter. The core materials should be emulsifiable in an aqueous solution. The melting point of the particles is less than about 100~C, preferably about 35~C to about 90~C and most preferably from about 45~C to about 85~C.
2 0 ~
In a preferred embodiment, a portion of the composite particles remain on the fabrics intact at the end of the drying cycle s;o that fragrance may be released while the - fabrics are being ironed or worn by the consumer.
The microcapsules of the present invention advantageously deposit a greater proportion of fragrance composition on drying clothes than prior art methods used in the art.
Additionally, less fragrance is lost during the manufacturing of the tumble drier article of the invention. Therefore, less of the perfume composition is needed to form the microcapsules to impart a greater proportion of perfume fragrance, such as the top notes of the perfume, on fabrics. Diffusion of fragrance is further significantly reduced during storage so that the fragrance is efficiently used for the purpose intended, rather than perfuming the environment.
The microcapsules are less than 100 microns in diameter, preferably about 3 to about 100 microns and most preferably about 3 to about 40 microns. The particles embedded in the microcapsules have an average diameter of about 5 microns and preferably less than 1 micron.
Spherical microcapsules are preferred, however, any geometric shape known in the art may be used within the scope of the invention.
Preferably the microcapsules are solid at room temperature but may also be in gel form.
2~87~' ~
The microcapsules of the present invention advantageously deposit a greater proportion of fragrance composition on drying clothes than prior art methods used in the art.
Additionally, less fragrance is lost during the manufacturing of the tumble drier article of the invention. Therefore, less of the perfume composition is needed to form the microcapsules to impart a greater proportion of perfume fragrance, such as the top notes of the perfume, on fabrics. Diffusion of fragrance is further significantly reduced during storage so that the fragrance is efficiently used for the purpose intended, rather than perfuming the environment.
The microcapsules are less than 100 microns in diameter, preferably about 3 to about 100 microns and most preferably about 3 to about 40 microns. The particles embedded in the microcapsules have an average diameter of about 5 microns and preferably less than 1 micron.
Spherical microcapsules are preferred, however, any geometric shape known in the art may be used within the scope of the invention.
Preferably the microcapsules are solid at room temperature but may also be in gel form.
2~87~' ~
Emulsifiable Material The term ~emulsifiable mixture~ is used to refer to a mixture of wax and perfume, optionally cont~;ning a surfactant, which forms an emulsion upon melting and dispersing into water, and has a melting point of less than about 100~C, preferably 35~C to 90~C and most preferably from 45~C to 85~C.
The melting point of the emulsifiable mixture is defined as the highest transition temperature (measurable by a conventional Differential Scanning Calorimeter) above the melting point at which the emulsifiable liquid becomes flowable or pourable.
The wax of the invention includes hydrocarbons such as paraffins and microcrystalline waxes. The optional surfactant includes cationic surfactants, preferably fabric softening materials; ethoxylated primary alcohol nonionic surfactants, preferably those derived from C16, C30, C40 or Cso average carbon chain length alcohols; anionic surfactants such as alkyl sulphonate, polymeric surfactants and mixtures thereof.
The paraffin and microcrystalline waxes used in the invention are preferably self-emulsifiable, but such self-emulsifiable waxes may be combined with non self-emulsifiable waxes to form a material within the scope of the invention.
Waxy materials which are contemplated within the scope of the present invention are presented in Table 1 below:
~ ~ 7 ~
The melting point of the emulsifiable mixture is defined as the highest transition temperature (measurable by a conventional Differential Scanning Calorimeter) above the melting point at which the emulsifiable liquid becomes flowable or pourable.
The wax of the invention includes hydrocarbons such as paraffins and microcrystalline waxes. The optional surfactant includes cationic surfactants, preferably fabric softening materials; ethoxylated primary alcohol nonionic surfactants, preferably those derived from C16, C30, C40 or Cso average carbon chain length alcohols; anionic surfactants such as alkyl sulphonate, polymeric surfactants and mixtures thereof.
The paraffin and microcrystalline waxes used in the invention are preferably self-emulsifiable, but such self-emulsifiable waxes may be combined with non self-emulsifiable waxes to form a material within the scope of the invention.
Waxy materials which are contemplated within the scope of the present invention are presented in Table 1 below:
~ ~ 7 ~
Self-Emulsifiable Waxy Materials Tvpe comPany Meltinq HLB saPoni-Desiqnation SuPplier Point Value fication Value Hydro- Duroxon* Duracheml 105-115 - 20-30 carbon J-324 Hydro- Duroxo* Durachem1 95-100 - 85-100 carbon B-120 Poly- Bestowa~ Duracheml - 38-45 ethylene AO-1539 Hydro- Durmont*E Durachem1 68-72 - 80 carbon Hydro- Carnauba* Duracheml 76-80 - 12-23 carbon PV-0553 Hydro- Durawax*S Durachem1 70-74 - 165-170 carbon Hydro- WS-215* Durachem1 48-50 - 19 carbon Nonionic Unithox* Petrolite2 91 4 Surfactant 420 Nonionic Unithox Petrolite2 90 10 Surfactant 450 Nonionic Unithox Petrolite2 105 10 35 Surfactant Non Self-Emulsifiable Waxy Materials Long C30-OH
Chain Alcohol Long C50-OH
Chain Alcohol 1Durachem - Dura Commodities Corp., Atlanta, GA
2Petrolite - Petrolite Speciality Polymers Group, Tulsa, OK
* denotes trade mark E
~ ~ 7 ~
Chain Alcohol Long C50-OH
Chain Alcohol 1Durachem - Dura Commodities Corp., Atlanta, GA
2Petrolite - Petrolite Speciality Polymers Group, Tulsa, OK
* denotes trade mark E
~ ~ 7 ~
A non self-emulsifiable wax such as Unilin*700 may be combined with a self-emulsifiable wax such as Duroxon J-324 in approximately equal ratios to form a material within the scope of the invention. The ratio of self-S emulsifiable ~ax to non self-emulsifiable wax is preferably in the range of about 1:3 to about 100% self-emulsifiable wax, and preferably about 1:1.
Another embodiment of the invention is the combination of a surfactant, such as a cationic fabric softening component with a paraffin wax in a ratio of about 1:1 fabric softening component to wax to form the particles in which the perfume composition is embedded.
lS Any conventional fabric softening component described below for use to form a tumble drier article may be used in combination with a wax or polymeric alcohol to form the particles of the microcapsules.
* denotes trade mark 207~71~
Another embodiment of the invention is the combination of a surfactant, such as a cationic fabric softening component with a paraffin wax in a ratio of about 1:1 fabric softening component to wax to form the particles in which the perfume composition is embedded.
lS Any conventional fabric softening component described below for use to form a tumble drier article may be used in combination with a wax or polymeric alcohol to form the particles of the microcapsules.
* denotes trade mark 207~71~
Water Soluble Polymers The water soluble polymers which are suitable for use in the invention include synthetic polymers and natural or modified natural polymers with molecular weights of less than 100,000.
Examples of synthetic water soluble polymers are:
(1) polyvinyl pyrrolidine;
(2) water sol-.~ble celluloses;
(3) polyvinyl alcohol;
(4) ethylene maleic anhydride copolymer;
(5) methyl vinyl ether maleic anhydride copolymer;
(6) polyethylene oxides;
(7) water soluble polyamide or polyester;
(8) copolymers or homopolymers of acrylic acid such as polyacrylic acid, polystyrene acrylic acid polymers or mixtures of two or more;
Examples of water-soluble hydroxylalkyl and carboxyalkyl cellulose include hydroxyethyl and carboxymethyl cellulose, hydroxyethyl, and carboxyethyl cellulose, hydroxymethyl and carboxymethyl cellulose, hydroxypropyl carboxymethyl cellulose, hydroxypropyl methyl carboxyethyl cellulose, hydroxypropyl carboxypropyl cellulose, hydroxybutyl carboxymethyl cellulose, and the like. Also useful are alkali metal salts of these carboxyalkyl 2 0 ~ ~ 7 ~ 7 celluloses, particularly and preferably the sodium and potassium salts.
;
Examples of water soluble natural and modified natural polymers are starch, gums and gelatin. Modified starch in its myriad of forms, including dextrins, is useful within the invention, as well as hydrolysed gums and hydrolysed gelatin. Various modified starches within the scope of the invention are described in Schoch et al., U.S. No.
2,876, 160.
Suitable hydrolysed gums within the invention include gum arabic, larch, pectin, tragacanth, locust bean, guar, alginates, carrageenans, cellulose gums such as carboxyl methyl cellulose and karaya.
Modified starch suitable for the invention has a dextrose equivalent of 0.25 up to about 20, preferably 5 to 15.
A wide range of starch hydrolysates having dextrose equivalents of up to 95 are also useful. Until recently these starch hydrolysates, also called maltodextrins and dextrins were produced from various starches by acid hydrolysis. The hydrolysates resulting from this acid process are not completely soluble in water, and contain native starch. Suitable starches are derived from corn, waxy maize, tapioca, etc.
~ ~ ~ 8 ~ ~ ~
Examples of synthetic water soluble polymers are:
(1) polyvinyl pyrrolidine;
(2) water sol-.~ble celluloses;
(3) polyvinyl alcohol;
(4) ethylene maleic anhydride copolymer;
(5) methyl vinyl ether maleic anhydride copolymer;
(6) polyethylene oxides;
(7) water soluble polyamide or polyester;
(8) copolymers or homopolymers of acrylic acid such as polyacrylic acid, polystyrene acrylic acid polymers or mixtures of two or more;
Examples of water-soluble hydroxylalkyl and carboxyalkyl cellulose include hydroxyethyl and carboxymethyl cellulose, hydroxyethyl, and carboxyethyl cellulose, hydroxymethyl and carboxymethyl cellulose, hydroxypropyl carboxymethyl cellulose, hydroxypropyl methyl carboxyethyl cellulose, hydroxypropyl carboxypropyl cellulose, hydroxybutyl carboxymethyl cellulose, and the like. Also useful are alkali metal salts of these carboxyalkyl 2 0 ~ ~ 7 ~ 7 celluloses, particularly and preferably the sodium and potassium salts.
;
Examples of water soluble natural and modified natural polymers are starch, gums and gelatin. Modified starch in its myriad of forms, including dextrins, is useful within the invention, as well as hydrolysed gums and hydrolysed gelatin. Various modified starches within the scope of the invention are described in Schoch et al., U.S. No.
2,876, 160.
Suitable hydrolysed gums within the invention include gum arabic, larch, pectin, tragacanth, locust bean, guar, alginates, carrageenans, cellulose gums such as carboxyl methyl cellulose and karaya.
Modified starch suitable for the invention has a dextrose equivalent of 0.25 up to about 20, preferably 5 to 15.
A wide range of starch hydrolysates having dextrose equivalents of up to 95 are also useful. Until recently these starch hydrolysates, also called maltodextrins and dextrins were produced from various starches by acid hydrolysis. The hydrolysates resulting from this acid process are not completely soluble in water, and contain native starch. Suitable starches are derived from corn, waxy maize, tapioca, etc.
~ ~ ~ 8 ~ ~ ~
Perfume comPositions The perfume composition of the emulsifiable mixture is characterized as an oil composition which is insoluble but water dispersible and may be either volatile or non-volatile. Perfume compositions should also be blended to impart aromas which compliment the products in which the microcapsules will be used. For example, tumble drier sheets may incorporate a lemon scent, woody scent, bouquet fragrance, etc. to impart the feeling of cleanliness and fine laundry.
Deofragrance compositions described in Hooper, U.S.
4,134,838 and 4,322,308 may be utilized within the present invention.
Perfume is released from the microcapsules and deposited on fabrics by at least partially dissolving the water soluble polymer of the microcapsules. Fragrance diffuses from the exposed or released particles. When the temperature is subsequently applied to the particles the wax is substantially melted and the perfume diffusion rate is accelerated.
In the preferred embodiment, water left in washed fabrics at the end of the drying cycle substantially dissolves the water soluble polymer of the microcapsules which have deposited on the fabrics mostly by mechanical action in the tumbling dryer. Subsequently as temperatures in the dryer rise from about 40~C upwards toward 60-90~C the wax of the deposited particles is substantially melted to release fragrance onto the fabrics at the end of the drying cycle. It may be understood that the skilled artisan may select waxes of higher melting points to 'E~
2~78717 control the release of the majority of the fragrance at the end of the cycle, within the scope of the invention.
In another aspect of the invention the microcapsules may be engineered to provide deposit of the microcapsules on dried fabrics and release of the fragrance only upon ironing using steam and high temperatures. Perspiration and body heat may also be used to release fragrance during wear by consumer, an embodiment of particular interest when deo-fragrance is used to form the particles.
2~717 Process The composite microcapsules are prepared by spray-drying an aqueous dispersion. The aqueous dispersion is formed by emulsifyin~ together the wax material and fragrance oil to form an emulsified mixture. In a reaction equipped with a stirrer, temperature controller and condenser. The reactor is heated and maintained at a temperature until the wax material and perfume are melted to form a smooth uniform solution. Water is then added to the uniform solution to form an aqueous wax/perfume emulsion. The emulsion is then cooled and the water soluble polymer is added to form a stable emulsion which is spray-dried to yield solid microcapsules containing particles of wax material and perfume.
If a surfactant is desired, it is added to the emulsified mixture in the reactor.
2~7~7~ ~
Deofragrance compositions described in Hooper, U.S.
4,134,838 and 4,322,308 may be utilized within the present invention.
Perfume is released from the microcapsules and deposited on fabrics by at least partially dissolving the water soluble polymer of the microcapsules. Fragrance diffuses from the exposed or released particles. When the temperature is subsequently applied to the particles the wax is substantially melted and the perfume diffusion rate is accelerated.
In the preferred embodiment, water left in washed fabrics at the end of the drying cycle substantially dissolves the water soluble polymer of the microcapsules which have deposited on the fabrics mostly by mechanical action in the tumbling dryer. Subsequently as temperatures in the dryer rise from about 40~C upwards toward 60-90~C the wax of the deposited particles is substantially melted to release fragrance onto the fabrics at the end of the drying cycle. It may be understood that the skilled artisan may select waxes of higher melting points to 'E~
2~78717 control the release of the majority of the fragrance at the end of the cycle, within the scope of the invention.
In another aspect of the invention the microcapsules may be engineered to provide deposit of the microcapsules on dried fabrics and release of the fragrance only upon ironing using steam and high temperatures. Perspiration and body heat may also be used to release fragrance during wear by consumer, an embodiment of particular interest when deo-fragrance is used to form the particles.
2~717 Process The composite microcapsules are prepared by spray-drying an aqueous dispersion. The aqueous dispersion is formed by emulsifyin~ together the wax material and fragrance oil to form an emulsified mixture. In a reaction equipped with a stirrer, temperature controller and condenser. The reactor is heated and maintained at a temperature until the wax material and perfume are melted to form a smooth uniform solution. Water is then added to the uniform solution to form an aqueous wax/perfume emulsion. The emulsion is then cooled and the water soluble polymer is added to form a stable emulsion which is spray-dried to yield solid microcapsules containing particles of wax material and perfume.
If a surfactant is desired, it is added to the emulsified mixture in the reactor.
2~7~7~ ~
Tumble Drier Article The formed composite microcapsules may be mixed with an effective amount of a fabric conditioning composition and coated onto a-dispensing means to form a tumble drier article. Such articles both condition fabrics in a tumble drier and impart a pleasant fragrance. The fabric conditioning composition has a preferred melting (or softening) point of about 35~C to about 150~C.
In one embodiment about 0.5% to about 80% of the composite microcapsules are mixed with the fabric conditioning composition, preferably about 1% to about 20%
microcapsules are mixed with the conditioning composition and most preferably about 2% to about 10% microcapsules are mixed with the conditioning composition. Because the fragrance is incorporated into the microcapsules, fragrance loss during manufacturing, storage and use is significantly reduced over sheets containing fragrance incorporated by conventional means and by other encapsulation technologies in the art.
The fabric conditioning composition which may be employed in the invention is coated onto a dispensing means which effectively releases the fabric conditioning composition in a tumble dryer. Such dispensing means can be designed for single usage or for multiple use. One such multi-use article comprises a sponge material releasably enclosing enough of the conditioning composition to impart effective fabric softning during several drying cycles. This multi-use article can be made by filling a porous sponge with the composition. In use, the composition melts and leaches out through the pores of the sponge to soften and condition fabrics. Such a filled sponge can be used to treat several loads of fabrics in conventional dryers, and 2078~ 7 has the advantage that it can remain in the dryer after use and is not likely to be misplaced or lost.
Another article comprises a cloth or paper bag releasably enclosing the~composition and sealed with a hardened plug of the mixture. The action and heat of the dryer opens the bag and releases the composition to perform its softening.
A highly preferred article comprises the compositions containing a softener and a compatible organosilicone releasably affixed to a flexible substrate such as a sheet of paper or woven or non-woven cloth substrate. When such an article is placed in an automatic laundry dryer, the heat, moisture, distribution forces and tumbling action of the dryer removes the composition from the substrate and deposits it on the fabrics.
The sheet conformation has several advantages. For example, effective amounts of the compositions for use in conventional dryers can be easily absorbed onto and into the sheet substrate by a simple dipping or padding process. Thus, the end user need not measure the amount of the composition necessary to obtain fabric softness and other benefits. Additionally, the flat configuration of the sheet provides a large surface are which results in efficient release and distribution of the materials onto fabrics by the tumbling action of the dryer.
The substrates used in the article can have a dense, or more preferably, open or porous structure. Examples of suitable materials which can be used as substrates herein include paper, woven cloth, and non-woven cloth. The term n cloth" herein means a woven or non-woven substrate for the articles of manufacture, as distinguished from the 2~7~ 7 term ~fabric~ which encompasses the clothing fabrics being dried in an automatic dryer.
It is known that most substances are able to absorb a liquid substance to some degree; however, the term ~absorbent~, as used herein, is intended to mean a substrate with an absorbent capacity (i.e., a parameter representing a substrate's ability to take up and retain a liquid) from 4 to 12, preferably 5 to 7 times its weight of water.
If the substrate is a foamed plastics material, the absorbent capacity is preferably in the range of 15 to 22, but some special foams can have an absorbent capacity in the range from 4 to 12.
Determination of absorbent capacity values is made by using the capacity testing procedures described in U.S.
Federal Specifications (W -T-595b), modified as follows:
1. tap water is used instead of distilled water;
2. the specimen is immersed for 30 seconds instead of 3 minutes;
3. draining time is 15 seconds instead of 1 minute; and 4. the specimen is immediately weighed on a torsion balance having a pan with turned-up edges.
Absorbent capacity values are then calculated in accordance with formulae given in said Specification.
Based on this test, one-ply, dense bleached paper ~e.g Kraft or bond having a basis weight of about 32 pounds per 3,000 square feet) has an absorbent capacity of 3.5 to 4;
2~7~?~17 commercially available household one-ply towel paper has a value of 5 to 6; and commercially available two-ply household towelling paper has a value of 7 to about 9.5.
Suitable mate~ials which can be used as a substrate in the invention herein include, among others, sponges, paper, and woven and non-woven cloth, all having the necessary absorbency requirement defined above.
The preferred non-woven cloth substrates can generally be defined as adhesively bonded fibrous or filamentous products having a web or carded fibre structure (where the fibre strength is suitable to allow carding), or comprising fibrous mats in which the fibres or filaments are distributed haphazardly or in r~n~om array (i.e. an array of fibres in a carded web wherein partial orientation of the fibres if frequently present, as well as a completely haphazard distributional orientation), or substantially aligned. The fibres or filaments can be natural (e.g. wool, silk, jute, hemp, cotton, linen, sisal, or ramie) or synthetic (e.g. rayon, cellulose ester, polyvinyl derivatives, polyolefins, polyamides, or polyesters).
The preferred absorbent properties are particularly easy to obtain with non-woven cloths and are provided merely by building up the thickness of the cloth, i.e., by superimposing a plurality of carded webs or mats to a thickness adequate to obtain the necessary absorbent properties, or by allowing a sufficient thickness of the fibres to deposit on the screen. A diameter or denier of the fibre (generally up to about 10 denier) can be used, inasmuch as it is the free space between each fibre that makes the thickness of the cloth directly related to the absorbent capacity of the cloth, and which, further, makes ~ ~ 7 ~
In one embodiment about 0.5% to about 80% of the composite microcapsules are mixed with the fabric conditioning composition, preferably about 1% to about 20%
microcapsules are mixed with the conditioning composition and most preferably about 2% to about 10% microcapsules are mixed with the conditioning composition. Because the fragrance is incorporated into the microcapsules, fragrance loss during manufacturing, storage and use is significantly reduced over sheets containing fragrance incorporated by conventional means and by other encapsulation technologies in the art.
The fabric conditioning composition which may be employed in the invention is coated onto a dispensing means which effectively releases the fabric conditioning composition in a tumble dryer. Such dispensing means can be designed for single usage or for multiple use. One such multi-use article comprises a sponge material releasably enclosing enough of the conditioning composition to impart effective fabric softning during several drying cycles. This multi-use article can be made by filling a porous sponge with the composition. In use, the composition melts and leaches out through the pores of the sponge to soften and condition fabrics. Such a filled sponge can be used to treat several loads of fabrics in conventional dryers, and 2078~ 7 has the advantage that it can remain in the dryer after use and is not likely to be misplaced or lost.
Another article comprises a cloth or paper bag releasably enclosing the~composition and sealed with a hardened plug of the mixture. The action and heat of the dryer opens the bag and releases the composition to perform its softening.
A highly preferred article comprises the compositions containing a softener and a compatible organosilicone releasably affixed to a flexible substrate such as a sheet of paper or woven or non-woven cloth substrate. When such an article is placed in an automatic laundry dryer, the heat, moisture, distribution forces and tumbling action of the dryer removes the composition from the substrate and deposits it on the fabrics.
The sheet conformation has several advantages. For example, effective amounts of the compositions for use in conventional dryers can be easily absorbed onto and into the sheet substrate by a simple dipping or padding process. Thus, the end user need not measure the amount of the composition necessary to obtain fabric softness and other benefits. Additionally, the flat configuration of the sheet provides a large surface are which results in efficient release and distribution of the materials onto fabrics by the tumbling action of the dryer.
The substrates used in the article can have a dense, or more preferably, open or porous structure. Examples of suitable materials which can be used as substrates herein include paper, woven cloth, and non-woven cloth. The term n cloth" herein means a woven or non-woven substrate for the articles of manufacture, as distinguished from the 2~7~ 7 term ~fabric~ which encompasses the clothing fabrics being dried in an automatic dryer.
It is known that most substances are able to absorb a liquid substance to some degree; however, the term ~absorbent~, as used herein, is intended to mean a substrate with an absorbent capacity (i.e., a parameter representing a substrate's ability to take up and retain a liquid) from 4 to 12, preferably 5 to 7 times its weight of water.
If the substrate is a foamed plastics material, the absorbent capacity is preferably in the range of 15 to 22, but some special foams can have an absorbent capacity in the range from 4 to 12.
Determination of absorbent capacity values is made by using the capacity testing procedures described in U.S.
Federal Specifications (W -T-595b), modified as follows:
1. tap water is used instead of distilled water;
2. the specimen is immersed for 30 seconds instead of 3 minutes;
3. draining time is 15 seconds instead of 1 minute; and 4. the specimen is immediately weighed on a torsion balance having a pan with turned-up edges.
Absorbent capacity values are then calculated in accordance with formulae given in said Specification.
Based on this test, one-ply, dense bleached paper ~e.g Kraft or bond having a basis weight of about 32 pounds per 3,000 square feet) has an absorbent capacity of 3.5 to 4;
2~7~?~17 commercially available household one-ply towel paper has a value of 5 to 6; and commercially available two-ply household towelling paper has a value of 7 to about 9.5.
Suitable mate~ials which can be used as a substrate in the invention herein include, among others, sponges, paper, and woven and non-woven cloth, all having the necessary absorbency requirement defined above.
The preferred non-woven cloth substrates can generally be defined as adhesively bonded fibrous or filamentous products having a web or carded fibre structure (where the fibre strength is suitable to allow carding), or comprising fibrous mats in which the fibres or filaments are distributed haphazardly or in r~n~om array (i.e. an array of fibres in a carded web wherein partial orientation of the fibres if frequently present, as well as a completely haphazard distributional orientation), or substantially aligned. The fibres or filaments can be natural (e.g. wool, silk, jute, hemp, cotton, linen, sisal, or ramie) or synthetic (e.g. rayon, cellulose ester, polyvinyl derivatives, polyolefins, polyamides, or polyesters).
The preferred absorbent properties are particularly easy to obtain with non-woven cloths and are provided merely by building up the thickness of the cloth, i.e., by superimposing a plurality of carded webs or mats to a thickness adequate to obtain the necessary absorbent properties, or by allowing a sufficient thickness of the fibres to deposit on the screen. A diameter or denier of the fibre (generally up to about 10 denier) can be used, inasmuch as it is the free space between each fibre that makes the thickness of the cloth directly related to the absorbent capacity of the cloth, and which, further, makes ~ ~ 7 ~
the non-woven cloth especially suitable for impregnation with a composition by means of intersectional or capillary action. Thus/ any thickness necessary to obtain the required absorbent capacity can be used.
s When the substrate for the composition is a non-woven cloth made from fibres deposited haphazardly in or random array on the screen, the articles exhibit excellent strength in all directions and are not prone to teat or separate when used in the automatic clothes dryer.
Preferably, the non-woven cloth is water-laid or air-laid and is made from cellulosic fibres, particularly from regenerated cellulose or rayon. Such non-woven cloth can be lubricated with any standard textile lubricant.
Preferably, the fibres are from Smm to 50mm in length and are from 1.5 to 5 denier. Preferably, the fibres are at least partially oriented haphazardly, and are adhesively bonded together with a hydrophobic or substantially hydrophobic binder-resin. Preferably, the cloth comprises about 70% fibre and 30% binder resin polymer by weight and has a basis weight of from about 18 to 45g per square meter.
In applying the fabric conditioning composition to the absorbent substrate, the amount impregnated into or coated onto the absorbent substrate is conveniently in the weight ratio range of from about 10:1 to 0.5:1 based on the ratio of total conditioning composition to dry, untreated substrate (fibre plus binder). Preferably, the amount of the conditioning composition ranges from about 5:1 to about 1:1, most preferably from about 3:1 to 1:1 by weight of the dry, untreated substrate.
2~7~17 According to one preferred embodiment of the invention, the dryer sheet substrate is coated by being passed over a rotogravure applicator roll. In its passage over this roll, the sheet is coated with a thin, uniform layer of molten fabric~softening composition contained in a rectangular pan at a level of about 12.5g/square metre.
Passage of the substrate over a cooling roll then solidifies the molten softening composition. This type of applicator is used to obtain a uniform homogeneous coating across the sheet.
Following application of the liquefied composition, the articles are held at room temperature until the composition substantially solidifies. The resulting dry articles, prepared at the composition substrate ratios set forth above, remain flexible; the sheet articles are suitable for packaging in rolls. The sheet articles can optionally be slitted or punched to provide a non-blocking aspect at any convenient time if desired during the manufacturing process.
The fabric conditioning composition employed in the present invention includes certain fabric softeners which can be used singly or in admixture with each other.
207~
s When the substrate for the composition is a non-woven cloth made from fibres deposited haphazardly in or random array on the screen, the articles exhibit excellent strength in all directions and are not prone to teat or separate when used in the automatic clothes dryer.
Preferably, the non-woven cloth is water-laid or air-laid and is made from cellulosic fibres, particularly from regenerated cellulose or rayon. Such non-woven cloth can be lubricated with any standard textile lubricant.
Preferably, the fibres are from Smm to 50mm in length and are from 1.5 to 5 denier. Preferably, the fibres are at least partially oriented haphazardly, and are adhesively bonded together with a hydrophobic or substantially hydrophobic binder-resin. Preferably, the cloth comprises about 70% fibre and 30% binder resin polymer by weight and has a basis weight of from about 18 to 45g per square meter.
In applying the fabric conditioning composition to the absorbent substrate, the amount impregnated into or coated onto the absorbent substrate is conveniently in the weight ratio range of from about 10:1 to 0.5:1 based on the ratio of total conditioning composition to dry, untreated substrate (fibre plus binder). Preferably, the amount of the conditioning composition ranges from about 5:1 to about 1:1, most preferably from about 3:1 to 1:1 by weight of the dry, untreated substrate.
2~7~17 According to one preferred embodiment of the invention, the dryer sheet substrate is coated by being passed over a rotogravure applicator roll. In its passage over this roll, the sheet is coated with a thin, uniform layer of molten fabric~softening composition contained in a rectangular pan at a level of about 12.5g/square metre.
Passage of the substrate over a cooling roll then solidifies the molten softening composition. This type of applicator is used to obtain a uniform homogeneous coating across the sheet.
Following application of the liquefied composition, the articles are held at room temperature until the composition substantially solidifies. The resulting dry articles, prepared at the composition substrate ratios set forth above, remain flexible; the sheet articles are suitable for packaging in rolls. The sheet articles can optionally be slitted or punched to provide a non-blocking aspect at any convenient time if desired during the manufacturing process.
The fabric conditioning composition employed in the present invention includes certain fabric softeners which can be used singly or in admixture with each other.
207~
Fabric Softener ComPonent Fabric softene!rs suitable for use herein are selected from the following classes of compounds:
(i) Cationic quaternary ~mmon;um salts. The counterion is methyl sulphate or any halide, methyl sulphate being preferred for the drier-added articles of the invention. Examples of cationic quaternary ammonium salts include, but are not limited to:
(1) Acyclic quaternary ammonium salts having at least two C830, preferably Cl222 alkyl rhA;nS~ such as:
ditallow dimethyl ammonium methylsulphate, di(hydrogenated tallow) dimethyl ammonium methylsulphate, distearyldimethyl ammonium methylsulphate, dicocodimethyl ammonium methylsulphate and the like;
(2) Cyclic quaternary ammonium salts of the imidazolinium type such as di(hydrogenated tallow) dimethyl imidazolinium methylsulphate, l-ethylene-bis(2-tallow-l-methyl) imidazolinium methylsulphate and the like;
(3) Diamido quaternary ammonium salts such as:
methyl-bis(hydrogenated tallow amidoethyl)-2-hydroxyethyl ammonium methyl sulphate, methyl bis(tallowamidoethyl)-2-hydroxypropyl ammonium methylsulphate and the like;
(4) Biodegradable quaternary ammonium salts such as N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium methyl sulphate and N,N-di(tallowoyl-oxy-propyl)-N,N-dimethyl ammonium methyl sulphate. When fabric conditioning compositions employ biodegradable quaternary ammonium salts, the pH of the composition is preferably adjusted to between about 2 and about 5. Biodegradable quaternary ammonium salts are described, for example, in U.S.
4,137,180; Patents 4,767,547 and 4,789,491.
(ii) Tertiary fatty amines having at least one and preferably two C8 to C30, preferably to Cl2 to C22, alkyl chains. Examples include hardened tallow amine and cyclic amines such as 1-(hydrogenated tallow)amidoethyl-2-(hydrogenated tallow) imidazoline. Cyclic amines whichmay be employed for the compositions herein are described in U.S. Patent 4,806,255.
(iii) Carboxylic acids having 8 to 30 carbon atoms and one carboxylic group per molecule. The alkyl portion has 8 to 30, preferably 12 to 22 carbon atoms. The alkyl portion may be linear or branched, saturated or unsaturated, with linear saturated alkyl preferred.
Stearic acid is a preferred fatty acid for use in the composition herein. Examples of these carboxylic acids are commercial grades of stearic acid and the like which may contain small amounts of other acids.
(iv) Esters of polyhydric alcohols such as sorbitan esters or glycerol stearate. Sorbitan esters are the condensation products of sorbitol or iso-sorbitol with fatty acids such as stearic acid. Preferred sorbitan esters are monoalkyl. A common example of sorbitan ester is SPAN*60 (ICI) which is a mixture of sorbitan and isosorbide stearates.
(v) Fatty alcohols, ethoxylated fatty alcohols, alkyl phenols, ethoxylated alkyl phenols, ethoxylated fatty amines, ethoxylated monoglycerides and ethoxylated diglycerides.
* denotes trade mark (vi) Mineral oils, and polyols such as polyethylene glycol.
i These softeners are more definitively described in U.S.
Patent 4,134,838. Preferred fabric softeners for use herein are acyclic quaternary ammonium salts, di(hydrogenated~tallow dimethyl ammonium methylsulphate is most preferred for dryer articles of this invention.
Especially preferred are mixtures of di(hydrogenated)tallow dimethyl ammonium methylsulphate with fatty acids, particularly stearic acid.
The amount of fabric softening composition on a sheet is subject to normal coating parameters such as, for example, viscosity and melting point, of the fabric softening component and is typically about 0.5 g to about 5 g, preferably about 1 g to about 3.5 g.
Optional ingredients include brighteners or fluorescent agents, colourants, germicides and bactericides.
The following examples will more fully illustrate the embodiments of this invention. All parts, percentages and proportions referred to herein and in the claims are by weight unless otherwise indicated.
~07g~ 7 Example 1 An emulsion con!taining a blend of a self-emulsifiable wax, a non self-emulsifiable wax and a perfume mixture dispersed in polyvinyl alcohol solution was prepared by the following process. 20g of the self-emulsifiable Duroxon J-324 wax (M.P. 105-115~C, Durachem), 20g of non self-emulsifiable Unilin 700 Wax (M.P. 110~C, Petrolite), 0.50g of potassium hydroxide and 20g of deionized water were charged to a 500ml reactor equipped with stirrer, temperature controller and condenser. The reactor was heated and maintained at 100~C until all the wax melted to form a smooth uniform solution. 16g of boiling deionized water was added slowly to the molten water mixture and the temperature was maintained at 100~C until a crystal clear solution was obser~ed. Following this, 44g of perfume (ex-Internatioanl Flavours & Fragrances~ was added slowly to the wax mixture at 100~C to yield a honey-like viscous solution. 80g of boiling deionized water was then added to the reactor to form a milky wax/perfume mixture emulsion. To this emulsion, 136g of polyvinyl alcohol solution (Molecular Weight 2,000, 17.6% solid) was added and the emulsion was cooled to 40-50~C with a water bath to form a stable emulsion. The resulting emulsion was spray dried at 120~C inlet air temperature using Yamato GA
31 minisprayer dryer to yield the microcapsule with 40%
perfume loading.
207~71 7 Example 2 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a polyvinylalcohol solution was S prepared as follows. To a 1 litre reactor equipped with stirrer, temperature cvntroller and condenser was charged 45g of self-emulsifiable Unithox 450 wax (m.p. 90~C, Petrolite). The reactor was heated and maintained at 95~C
until all the wax melt. 90g of perfume (ex-IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 222g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. 390g of polyvinylalcohol solution (Molecular Weight 2,000, 23.1% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 150~C inlet air temperature and 70~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 40% perfume loading.
2 ~ 7 Example 3 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a polyvinylalcohol solution was prepared as fallows. To a 1 litre reactor equipped with stirrer, temperature controller and condenser was charged 22.5g of Unithox 450 wax and 22.5g of ditallowdimethylammonium methylsulphate. The reactor was heated and maintained at 95~C until all the wax melted.
90g of perfume (ex- IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 222g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. 390g of polyvinylalcohol solution (Molecular Weight2,000, 23.1% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 150~C inlet air temperature and 70~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 40%
perfume loading.
'~
(i) Cationic quaternary ~mmon;um salts. The counterion is methyl sulphate or any halide, methyl sulphate being preferred for the drier-added articles of the invention. Examples of cationic quaternary ammonium salts include, but are not limited to:
(1) Acyclic quaternary ammonium salts having at least two C830, preferably Cl222 alkyl rhA;nS~ such as:
ditallow dimethyl ammonium methylsulphate, di(hydrogenated tallow) dimethyl ammonium methylsulphate, distearyldimethyl ammonium methylsulphate, dicocodimethyl ammonium methylsulphate and the like;
(2) Cyclic quaternary ammonium salts of the imidazolinium type such as di(hydrogenated tallow) dimethyl imidazolinium methylsulphate, l-ethylene-bis(2-tallow-l-methyl) imidazolinium methylsulphate and the like;
(3) Diamido quaternary ammonium salts such as:
methyl-bis(hydrogenated tallow amidoethyl)-2-hydroxyethyl ammonium methyl sulphate, methyl bis(tallowamidoethyl)-2-hydroxypropyl ammonium methylsulphate and the like;
(4) Biodegradable quaternary ammonium salts such as N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium methyl sulphate and N,N-di(tallowoyl-oxy-propyl)-N,N-dimethyl ammonium methyl sulphate. When fabric conditioning compositions employ biodegradable quaternary ammonium salts, the pH of the composition is preferably adjusted to between about 2 and about 5. Biodegradable quaternary ammonium salts are described, for example, in U.S.
4,137,180; Patents 4,767,547 and 4,789,491.
(ii) Tertiary fatty amines having at least one and preferably two C8 to C30, preferably to Cl2 to C22, alkyl chains. Examples include hardened tallow amine and cyclic amines such as 1-(hydrogenated tallow)amidoethyl-2-(hydrogenated tallow) imidazoline. Cyclic amines whichmay be employed for the compositions herein are described in U.S. Patent 4,806,255.
(iii) Carboxylic acids having 8 to 30 carbon atoms and one carboxylic group per molecule. The alkyl portion has 8 to 30, preferably 12 to 22 carbon atoms. The alkyl portion may be linear or branched, saturated or unsaturated, with linear saturated alkyl preferred.
Stearic acid is a preferred fatty acid for use in the composition herein. Examples of these carboxylic acids are commercial grades of stearic acid and the like which may contain small amounts of other acids.
(iv) Esters of polyhydric alcohols such as sorbitan esters or glycerol stearate. Sorbitan esters are the condensation products of sorbitol or iso-sorbitol with fatty acids such as stearic acid. Preferred sorbitan esters are monoalkyl. A common example of sorbitan ester is SPAN*60 (ICI) which is a mixture of sorbitan and isosorbide stearates.
(v) Fatty alcohols, ethoxylated fatty alcohols, alkyl phenols, ethoxylated alkyl phenols, ethoxylated fatty amines, ethoxylated monoglycerides and ethoxylated diglycerides.
* denotes trade mark (vi) Mineral oils, and polyols such as polyethylene glycol.
i These softeners are more definitively described in U.S.
Patent 4,134,838. Preferred fabric softeners for use herein are acyclic quaternary ammonium salts, di(hydrogenated~tallow dimethyl ammonium methylsulphate is most preferred for dryer articles of this invention.
Especially preferred are mixtures of di(hydrogenated)tallow dimethyl ammonium methylsulphate with fatty acids, particularly stearic acid.
The amount of fabric softening composition on a sheet is subject to normal coating parameters such as, for example, viscosity and melting point, of the fabric softening component and is typically about 0.5 g to about 5 g, preferably about 1 g to about 3.5 g.
Optional ingredients include brighteners or fluorescent agents, colourants, germicides and bactericides.
The following examples will more fully illustrate the embodiments of this invention. All parts, percentages and proportions referred to herein and in the claims are by weight unless otherwise indicated.
~07g~ 7 Example 1 An emulsion con!taining a blend of a self-emulsifiable wax, a non self-emulsifiable wax and a perfume mixture dispersed in polyvinyl alcohol solution was prepared by the following process. 20g of the self-emulsifiable Duroxon J-324 wax (M.P. 105-115~C, Durachem), 20g of non self-emulsifiable Unilin 700 Wax (M.P. 110~C, Petrolite), 0.50g of potassium hydroxide and 20g of deionized water were charged to a 500ml reactor equipped with stirrer, temperature controller and condenser. The reactor was heated and maintained at 100~C until all the wax melted to form a smooth uniform solution. 16g of boiling deionized water was added slowly to the molten water mixture and the temperature was maintained at 100~C until a crystal clear solution was obser~ed. Following this, 44g of perfume (ex-Internatioanl Flavours & Fragrances~ was added slowly to the wax mixture at 100~C to yield a honey-like viscous solution. 80g of boiling deionized water was then added to the reactor to form a milky wax/perfume mixture emulsion. To this emulsion, 136g of polyvinyl alcohol solution (Molecular Weight 2,000, 17.6% solid) was added and the emulsion was cooled to 40-50~C with a water bath to form a stable emulsion. The resulting emulsion was spray dried at 120~C inlet air temperature using Yamato GA
31 minisprayer dryer to yield the microcapsule with 40%
perfume loading.
207~71 7 Example 2 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a polyvinylalcohol solution was S prepared as follows. To a 1 litre reactor equipped with stirrer, temperature cvntroller and condenser was charged 45g of self-emulsifiable Unithox 450 wax (m.p. 90~C, Petrolite). The reactor was heated and maintained at 95~C
until all the wax melt. 90g of perfume (ex-IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 222g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. 390g of polyvinylalcohol solution (Molecular Weight 2,000, 23.1% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 150~C inlet air temperature and 70~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 40% perfume loading.
2 ~ 7 Example 3 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a polyvinylalcohol solution was prepared as fallows. To a 1 litre reactor equipped with stirrer, temperature controller and condenser was charged 22.5g of Unithox 450 wax and 22.5g of ditallowdimethylammonium methylsulphate. The reactor was heated and maintained at 95~C until all the wax melted.
90g of perfume (ex- IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 222g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. 390g of polyvinylalcohol solution (Molecular Weight2,000, 23.1% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 150~C inlet air temperature and 70~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 40%
perfume loading.
'~
ExamPle 4 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a polyvinylalcohol solution was prepared as follows. To a 1 litre reactor equipped with stirrer, temperature controller and condenser was charged 45g of self-emulsifiable Unithox 750 wax (m.p. 110~C, Petrolite). The reactor was heated and maintained at 95~C
until all the wax melted. 90g of perfume (ex- IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 222g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. 390g of polyvinylalcohol solution (Molecular Weight 2,000, 23.1% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 150~C inlet air temperature and 70~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 40% perfume loading.
2 ~ C6150 Example 5 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a hydrophobically modified starch solution was prepared as follows. To a 500ml reactor equipped with stirrer, temperature controller and condenser was charged 30g of self-emulsifiable Unithox 450 wax (m.p. 90~C, Petrolite). The reactor was heated and maintained at 95~C until all the wax melted. 60g of perfume ~ex- IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 90g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. lOOg of Capsul*solution (National Starch and Chemical Corp., 30% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 120~C inlet air temperature and 60~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 50%
perfume loading.
* denotes trade mark Characteristics of CaPsules The composition and the characteristics of the prepared capsules are shown in Table I. The % washable perfume oil is determined by washing the capsule with n-hexane. Two grams of capsule are weighed into a Buchner funnel. 40g of hexane is added to the funnel. The hexane is removed by applying vacuum and the washed capsule is air dried to a constant weight. The % washable oil is then calculated from the amount of perfume oil removed and the total oil contained in the capsule.
Table I
15 CaPsule ComPosition % Washable Oil Example 1 40.8% Perfume, 18.6% Duroxon J-324 44%
18.6% Uniline*700, 22% PVA
Example 2 40% Perfume, 20% Unithox 450 1.3%
40% PVA
Example 3 40% Perfume, 10% Unithox 450 1.6%
10% Ditallowdimethylammonium Methyl Sulfate 40% PVA
Example 4 40% Perfume, 20% Unithox 750 3.75%
40% PVA
Example 5 50% Perfume, 25% Unithox 450 66%
25% Capsul~ R) * denotes trade mark .~
~Q7~~~17 Example 6 This example gi;ves a comparison of the result obtained by using a mixture of nonemulsifiable core material for the preparation of perfume/wax microcapsules by the same process described in example 2. l9g of C30 alcohol (Uniline 425, ex-Petrolite) was charged into a 500ml reactor. The reactor was heated and maintained at 95~C
until all the wax melted. l9g of perfume (ex IFF) was added slowly to the molten wax and the temperature was maintained at 90~C to form a clear solution. 114g of hot deionized water was then added to the reactor. Following this addition, 152g of polyvinylalcohol solution (25%
solid, 2,000 MW) was added to the reactor and the reactor was cooled to 40~C with a water bath. It was observed that instead of forming a stable emulsion, the wax/perfume mixture formed large aggregates which could not be spray dried.
_ 33 - 207~ 17C6150 Exam~le 7 A wax and perfume mixture was encapsulated in a modified starch Capsul (ex-National Starch and Chemical Corp.) using the process described in U.S. Patent 3,091,567.
Capsul is a modified food starch derived from waxy maize especially designed for spray drying encapsulation of perfumes and flavours. 40g of Capsul and 160g of deionized water were added to a 500ml reactor. The reactor was hea~ed and maintained at 90~C until all the Capsul dissolved. At the same time, a wax and perfume mixture was prepared by melting 20g of Uniline 425 wax ~ex-Petrolite) and 20g of perfume (ex-IFF) at 90~C. The wax and perfume mixture was added to the reactor and agitated with the Capsul solution at 90~C for 30 minutes.
The resulting emulsion was then cooled to 40~C with a water bath. Rather than forming a stable emulsion, the wax and perfume mixture formed large aggregates which could not be spray dried.
2Q7~717 Exam~le 8 Microcapsules were formed using polyvinyl alcohol by the process described in Example 2. In this example, the core material is perfume only, without wax. 40g of perfume (ex-IFF) was emulsified into 164g of polyvinyl alcohol (24.5% solid, 2,000 M.W.) to form a stable perfume emulsion. The perfume emulsion was spray dried at 120~
inlet air temperature and 60~C outlet air temperature using Yamato GA31 minispray dryer. The sprayed emulsion was heavily coated on the wall of drying chamber and could not be used to produce free flowing perfume capsules.
2 ~ 7 ~ ~ ~7 Exam~le 9: Fabric Softener Sheet Pre~aration Fabric softener dryer sheets comprising a perfume-containing fabric softener composition coated on a polyester substrate were prepared as follows. The perfume-contA; n; ng softener active composition was prepared by admixing 36 grams of perfume microcapsule with 900 grams of molten softener active comprising 70 wt.%
ditallowdimethylammonium methylsulphate and 30 wt.% Cl6l8 fatty acid at 75~C for 4-6 minutes. After the addition was completed, the molten softener active was transferred to a 3-roller Lyons Bench Coater preheated to 79~C. The molten softener active was then coated on 9 inches by 11 inches polyester substrate with a coating weight 1.6 grams per sheet. The perfume microcapsules of Example 2 and Example 3 were used for the sheet preparation. The same procedure was also used to make one softener sheet containing 4 wt.% of free perfume oil.
Example 10: Fabric Perfume Odour Test This test compares the effectiveness of perfume microcapsule vs. free (non-encapsulated) perfume oil in perfume substantivity to fabric after a dryer cycle. In this test, 6 lbs. of freshly washed fabrics are dried for 40 minutes in a Kenmore electric dryer (Lady Kenmore)*.
At the start of the drying cycle, 9 inches of 11 inches of perfume-containing fabric softener sheet is placed on the top of the clothes. Two dryers are used for the test. In one drier the sheet containing the free perfume oil is used while the other drier contains the perfume microcapsule. At the end of the drying cycle, the fabrics are removed from the dryer. The odour from the treated fabrics is compared. Evaluation results (Table II) show that fabrics treated with the sheet containing either Example 2 or Example 3 microcapsules gave stronger perfume odour than those treated with the sheet containing the free perfume oil even at a lower total perfume level (1.6 wt.% vs. 4 wt.%).
Table II
% Perfume % Perfume CaPsule Perfume Odour Sheet 1 4% None Weak Sheet 2 1.6% 4% Example 2 Stronger Sheet 3 1.6% 4% Example 3 Stronger * denotes trade mark '~'
until all the wax melted. 90g of perfume (ex- IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 222g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. 390g of polyvinylalcohol solution (Molecular Weight 2,000, 23.1% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 150~C inlet air temperature and 70~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 40% perfume loading.
2 ~ C6150 Example 5 An emulsion containing a blend of self-emulsifiable wax and perfume dispersed in a hydrophobically modified starch solution was prepared as follows. To a 500ml reactor equipped with stirrer, temperature controller and condenser was charged 30g of self-emulsifiable Unithox 450 wax (m.p. 90~C, Petrolite). The reactor was heated and maintained at 95~C until all the wax melted. 60g of perfume ~ex- IFF) was added slowly to the reactor for a period of 5 to 8 minutes and the temperature was maintained at 90~C to form a clear solution. Following this, 90g of hot deionized water (90~C) was added to the mixture of molten wax and perfume to form a milky emulsion. lOOg of Capsul*solution (National Starch and Chemical Corp., 30% solid) was added to the reactor and the emulsion was cooled to 40-50~C with a water bath. The resulting emulsion was then spray dried at 120~C inlet air temperature and 60~C air outlet temperature using Yamato GA31 minispray dryer to make the microcapsule with 50%
perfume loading.
* denotes trade mark Characteristics of CaPsules The composition and the characteristics of the prepared capsules are shown in Table I. The % washable perfume oil is determined by washing the capsule with n-hexane. Two grams of capsule are weighed into a Buchner funnel. 40g of hexane is added to the funnel. The hexane is removed by applying vacuum and the washed capsule is air dried to a constant weight. The % washable oil is then calculated from the amount of perfume oil removed and the total oil contained in the capsule.
Table I
15 CaPsule ComPosition % Washable Oil Example 1 40.8% Perfume, 18.6% Duroxon J-324 44%
18.6% Uniline*700, 22% PVA
Example 2 40% Perfume, 20% Unithox 450 1.3%
40% PVA
Example 3 40% Perfume, 10% Unithox 450 1.6%
10% Ditallowdimethylammonium Methyl Sulfate 40% PVA
Example 4 40% Perfume, 20% Unithox 750 3.75%
40% PVA
Example 5 50% Perfume, 25% Unithox 450 66%
25% Capsul~ R) * denotes trade mark .~
~Q7~~~17 Example 6 This example gi;ves a comparison of the result obtained by using a mixture of nonemulsifiable core material for the preparation of perfume/wax microcapsules by the same process described in example 2. l9g of C30 alcohol (Uniline 425, ex-Petrolite) was charged into a 500ml reactor. The reactor was heated and maintained at 95~C
until all the wax melted. l9g of perfume (ex IFF) was added slowly to the molten wax and the temperature was maintained at 90~C to form a clear solution. 114g of hot deionized water was then added to the reactor. Following this addition, 152g of polyvinylalcohol solution (25%
solid, 2,000 MW) was added to the reactor and the reactor was cooled to 40~C with a water bath. It was observed that instead of forming a stable emulsion, the wax/perfume mixture formed large aggregates which could not be spray dried.
_ 33 - 207~ 17C6150 Exam~le 7 A wax and perfume mixture was encapsulated in a modified starch Capsul (ex-National Starch and Chemical Corp.) using the process described in U.S. Patent 3,091,567.
Capsul is a modified food starch derived from waxy maize especially designed for spray drying encapsulation of perfumes and flavours. 40g of Capsul and 160g of deionized water were added to a 500ml reactor. The reactor was hea~ed and maintained at 90~C until all the Capsul dissolved. At the same time, a wax and perfume mixture was prepared by melting 20g of Uniline 425 wax ~ex-Petrolite) and 20g of perfume (ex-IFF) at 90~C. The wax and perfume mixture was added to the reactor and agitated with the Capsul solution at 90~C for 30 minutes.
The resulting emulsion was then cooled to 40~C with a water bath. Rather than forming a stable emulsion, the wax and perfume mixture formed large aggregates which could not be spray dried.
2Q7~717 Exam~le 8 Microcapsules were formed using polyvinyl alcohol by the process described in Example 2. In this example, the core material is perfume only, without wax. 40g of perfume (ex-IFF) was emulsified into 164g of polyvinyl alcohol (24.5% solid, 2,000 M.W.) to form a stable perfume emulsion. The perfume emulsion was spray dried at 120~
inlet air temperature and 60~C outlet air temperature using Yamato GA31 minispray dryer. The sprayed emulsion was heavily coated on the wall of drying chamber and could not be used to produce free flowing perfume capsules.
2 ~ 7 ~ ~ ~7 Exam~le 9: Fabric Softener Sheet Pre~aration Fabric softener dryer sheets comprising a perfume-containing fabric softener composition coated on a polyester substrate were prepared as follows. The perfume-contA; n; ng softener active composition was prepared by admixing 36 grams of perfume microcapsule with 900 grams of molten softener active comprising 70 wt.%
ditallowdimethylammonium methylsulphate and 30 wt.% Cl6l8 fatty acid at 75~C for 4-6 minutes. After the addition was completed, the molten softener active was transferred to a 3-roller Lyons Bench Coater preheated to 79~C. The molten softener active was then coated on 9 inches by 11 inches polyester substrate with a coating weight 1.6 grams per sheet. The perfume microcapsules of Example 2 and Example 3 were used for the sheet preparation. The same procedure was also used to make one softener sheet containing 4 wt.% of free perfume oil.
Example 10: Fabric Perfume Odour Test This test compares the effectiveness of perfume microcapsule vs. free (non-encapsulated) perfume oil in perfume substantivity to fabric after a dryer cycle. In this test, 6 lbs. of freshly washed fabrics are dried for 40 minutes in a Kenmore electric dryer (Lady Kenmore)*.
At the start of the drying cycle, 9 inches of 11 inches of perfume-containing fabric softener sheet is placed on the top of the clothes. Two dryers are used for the test. In one drier the sheet containing the free perfume oil is used while the other drier contains the perfume microcapsule. At the end of the drying cycle, the fabrics are removed from the dryer. The odour from the treated fabrics is compared. Evaluation results (Table II) show that fabrics treated with the sheet containing either Example 2 or Example 3 microcapsules gave stronger perfume odour than those treated with the sheet containing the free perfume oil even at a lower total perfume level (1.6 wt.% vs. 4 wt.%).
Table II
% Perfume % Perfume CaPsule Perfume Odour Sheet 1 4% None Weak Sheet 2 1.6% 4% Example 2 Stronger Sheet 3 1.6% 4% Example 3 Stronger * denotes trade mark '~'
Claims (22)
1. A tumble drier article of manufacture adapted for conditioning fabric in an automatic clothes drier comprising:
(a) a fabric softening composition comprising a fabric softener selected from the group consisting of: cationic quaternary ammonium salts, tertiary fatty amines having at least one C8 to C30, alkyl groups, carboxylic acids having 8 to 30 carbon atoms and one carboxy group per molecule, esters of polyhydric alcohols, fatty alcohols, ethoxylated fatty alcohols, alkyl phenols, ethoxylated alkyl phenols, ethoxylated fatty amines, ethoxylated monoglycerides, ethoxylated diglycerides, mineral oils, polyols and mixtures thereof;
(b) between 0.5 and 80% by weight of spray dried composite microcapsules having a diameter less than 100 micrometers, each microcapsule material comprising individual particles of an emulsifiable mixture of wax material and a perfume composition, the mixture having a melting point between 35 and 90°C and a water soluble polymer wherein the wax material and the perfume composition are dispersed in the water soluble polymer, and the individual particles of the mixture of wax and perfume composition having an average diameter of less than 5 micrometers;
(c) dispensing means for releasing the fabric softening composition and the microcapsules onto fabrics, the fabric softening composition being releasably attached to the dispensing means in a weight ratio of from 10:1 to 0.5:1 of the fabric softening composition to the dispensing means.
(a) a fabric softening composition comprising a fabric softener selected from the group consisting of: cationic quaternary ammonium salts, tertiary fatty amines having at least one C8 to C30, alkyl groups, carboxylic acids having 8 to 30 carbon atoms and one carboxy group per molecule, esters of polyhydric alcohols, fatty alcohols, ethoxylated fatty alcohols, alkyl phenols, ethoxylated alkyl phenols, ethoxylated fatty amines, ethoxylated monoglycerides, ethoxylated diglycerides, mineral oils, polyols and mixtures thereof;
(b) between 0.5 and 80% by weight of spray dried composite microcapsules having a diameter less than 100 micrometers, each microcapsule material comprising individual particles of an emulsifiable mixture of wax material and a perfume composition, the mixture having a melting point between 35 and 90°C and a water soluble polymer wherein the wax material and the perfume composition are dispersed in the water soluble polymer, and the individual particles of the mixture of wax and perfume composition having an average diameter of less than 5 micrometers;
(c) dispensing means for releasing the fabric softening composition and the microcapsules onto fabrics, the fabric softening composition being releasably attached to the dispensing means in a weight ratio of from 10:1 to 0.5:1 of the fabric softening composition to the dispensing means.
2. The tumble drier article according to claim 1 wherein the water soluble polymer is selected from the group consisting of a synthetic polymer, a natural polymer or modified natural polymer having a molecular weight of less than 100,000 and mixtures thereof.
3. The tumble drier article according to claim 1 wherein the wax material is selected from the group consisting of a hydrocarbon based paraffin wax and a hydrocarbon based microcrystalline wax.
4. The tumble drier article according to claim 1 wherein the emulsifiable mixture of wax and perfume composition further comprises a surfactant.
5. The tumble drier article according to claim 4, wherein the surfactant is a nonionic surfactant derived from C16, C30, C40 or C50 average carbon chain length alcohols, a cationic fabric softening component, or mixtures thereof.
6. The tumble drier article according to claim 4, wherein the surfactant is an ethoxylated primary alcohol or a cationic fabric softening compound.
7. The tumble drier article according to claim 1, wherein the water soluble polymer is a synthetic polymer and is a material selected from the group consisting of polyvinyl pyrrolidine, a water soluble cellulose, a polyvinyl alcohol, a polyethylene oxide, a homo- or copolymer of acrylic acid or methacrylic acid or mixtures thereof, ethylene maleic anhydride copolymer, methyl vinyl ether maleic anhydride copolymer, a water soluble polyamide or polyester, or mixtures thereof.
8. The tumble drier article according to claim 7 wherein the synthetic polymer is polyvinyl pyrrolidine or polyvinyl alcohol.
9. A tumble drier article according to claim 2 wherein the natural polymer is a starch, a gum, or a gelatin.
10. A tumble drier article according to claim 1 wherein each microcapsule has a diameter of 3 to 100 micrometers.
11. A tumble drier article according to claim 10 wherein each of the microcapsules has a diameter of about 3 to about 40 micrometers.
12. A tumble drier article according to claim 1 wherein the particles have an average diameter of less than about 1 micrometer.
13. A composite microcapsule containing a fragrance oil comprising:
(a) particles composed of an emulsifiable mixture of a self-emulsifiable wax material and optionally, a non-self-emulsifiable wax material, and a perfume composition, the mixture having a melting point between 35 and 90°C, the ratio of self-emulsifiable to non-self-emulsifiable wax being at least 1:3, the particles having an average diameter of less than 5 micrometers; and (b) a water soluble polymer encapsulating the particles to form composite microcapsules having a diameter less than 100 micrometers whereby the fragrance oil is released by dissolving the polymer upon contact with a liquid and melting the wax material at a temperature below 90°C, the microcapsules having been formed by a spray drying process.
(a) particles composed of an emulsifiable mixture of a self-emulsifiable wax material and optionally, a non-self-emulsifiable wax material, and a perfume composition, the mixture having a melting point between 35 and 90°C, the ratio of self-emulsifiable to non-self-emulsifiable wax being at least 1:3, the particles having an average diameter of less than 5 micrometers; and (b) a water soluble polymer encapsulating the particles to form composite microcapsules having a diameter less than 100 micrometers whereby the fragrance oil is released by dissolving the polymer upon contact with a liquid and melting the wax material at a temperature below 90°C, the microcapsules having been formed by a spray drying process.
14. The composite microcapsule according to claim 13, wherein the emulsifiable mixture comprises a wax selected from the group consisting of a hydrocarbon based paraffin wax and a hydrocarbon based microcrystalline wax.
15. The composite microcapsule according to claim 13, wherein the emulsifiable mixture further comprises a surfactant selected from the group consisting of a nonionic surfactant derived from C16, C30, C40 or C50 average carbon chain length alcohols, a cationic fabric softening component, or mixtures thereof.
16. The composite microcapsule according to claim 13, wherein the water soluble polymer is a synthetic polymer, natural polymer or a modified natural polymer.
17. The composite microcapsule according to claim 16, wherein the synthetic polymer is a material selected from the group consisting of polyvinyl pyrrolidine, a water soluble cellulose, a polyvinyl alcohol, a polyethylene oxide, a homo- or copolymer of acrylic acid or methacrylic acid or mixtures thereof, ethylene maleic anhydride copolymer, methyl vinyl ether maleic anhydride copolymer, a water soluble polyamide or polyester, or mixtures thereof.
18. The composite microcapsule article according to claim 13 wherein each microcapsule has a diameter of about 3 to 100 micrometers.
19. The composite microcapsule article according to claim 18 wherein each of the microcapsules has a diameter of 3 to 40 micrometers.
20. The composite microcapsules according to any one of claims 13 to 19 wherein the microcapsules are solid or in gel form at room temperature.
21. A composite microcapsule article according to claim 13 wherein the ratio of wax material to the fragrance oil is 1:4 to 4:1.
22. A process for making a composite microcapsule of claim 13 comprising the steps of:
(a) selecting a self-emulsifiable wax material and, optionally, a non-self emulsifiable wax material and a perfume composition to form an emulsifiable mixture having a melting point of between 35° and 90°C, the ratio by weight of self-emulsifiable to non-self-emulsifiable wax material being at least 1:3;
(b) selecting a water-soluble polymer;
(c) melting the emulsifiable mixture in a reactor until a uniform solution is obtained;
(d) adding water to the uniform solution to form an aqueous emulsion;
(e) adding the water soluble polymer to the aqueous emulsion and cooling the resulting mixture to form a stable emulsion;
(f) spray drying the stable emulsion to yield a composite microcapsule having a diameter of less than 100 micrometers.
(a) selecting a self-emulsifiable wax material and, optionally, a non-self emulsifiable wax material and a perfume composition to form an emulsifiable mixture having a melting point of between 35° and 90°C, the ratio by weight of self-emulsifiable to non-self-emulsifiable wax material being at least 1:3;
(b) selecting a water-soluble polymer;
(c) melting the emulsifiable mixture in a reactor until a uniform solution is obtained;
(d) adding water to the uniform solution to form an aqueous emulsion;
(e) adding the water soluble polymer to the aqueous emulsion and cooling the resulting mixture to form a stable emulsion;
(f) spray drying the stable emulsion to yield a composite microcapsule having a diameter of less than 100 micrometers.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US766477 | 1985-08-19 | ||
| US07/766,477 US5246603A (en) | 1991-09-25 | 1991-09-25 | Fragrance microcapsules for fabric conditioning |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2078717A1 CA2078717A1 (en) | 1993-03-26 |
| CA2078717C true CA2078717C (en) | 1999-01-12 |
Family
ID=25076543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002078717A Expired - Lifetime CA2078717C (en) | 1991-09-25 | 1992-09-21 | Fragrance microcapsules for fabric conditioning |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5246603A (en) |
| EP (1) | EP0539025B1 (en) |
| JP (1) | JP2837042B2 (en) |
| AU (1) | AU664859B2 (en) |
| CA (1) | CA2078717C (en) |
| DE (1) | DE69227883T2 (en) |
| ES (1) | ES2124720T3 (en) |
Families Citing this family (82)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5770319A (en) * | 1990-08-23 | 1998-06-23 | Her Majesty The Queen In Right Of New Zealand | Densification of lignocellulosic material |
| US5425887A (en) * | 1993-07-26 | 1995-06-20 | Lever Brothers Company, Division Of Conopco, Inc. | Encapsualted perfume in fabric conditioning articles |
| US5480567A (en) * | 1994-01-14 | 1996-01-02 | Lever Brothers Company, Division Of Conopco, Inc. | Surfactant mixtures for fabric conditioning compositions |
| US5630847A (en) * | 1995-03-30 | 1997-05-20 | The Procter & Gamble Company | Perfumable dry cleaning and spot removal process |
| DE19603453C1 (en) * | 1996-01-31 | 1997-10-02 | Fraunhofer Ges Forschung | Microparticles containing an active ingredient and a polymeric capsule wall material, a process for their production and their use |
| JP2000512671A (en) | 1996-06-14 | 2000-09-26 | エミスフェアー テクノロジーズ インク | Microencapsulated fragrance and preparation method |
| JP3304776B2 (en) * | 1996-07-08 | 2002-07-22 | トヨタ自動車株式会社 | Vehicle wheel grip determination device |
| US6297210B1 (en) * | 1999-04-23 | 2001-10-02 | Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. | Process for applying perfume to dryer sheets |
| US6689740B1 (en) * | 1999-06-15 | 2004-02-10 | Givaudan Sa | Method for preparing fragrance products |
| JP2003511517A (en) * | 1999-10-05 | 2003-03-25 | ザ、プロクター、エンド、ギャンブル、カンパニー | Elastic products |
| US6200949B1 (en) * | 1999-12-21 | 2001-03-13 | International Flavors And Fragrances Inc. | Process for forming solid phase controllably releasable fragrance-containing consumable articles |
| DE10044382A1 (en) | 2000-09-08 | 2002-04-04 | Haarmann & Reimer Gmbh | care products |
| US6531444B1 (en) | 2000-11-09 | 2003-03-11 | Salvona, Llc | Controlled delivery system for fabric care products |
| DE10105801B4 (en) * | 2001-02-07 | 2004-07-08 | Henkel Kgaa | Detergents and cleaning agents comprising fine microparticles with detergent components |
| EP1243326A1 (en) * | 2001-03-22 | 2002-09-25 | Cognis Iberia, S.L. | Nanocapsules (II) |
| EP1243325A1 (en) * | 2001-03-22 | 2002-09-25 | Cognis Iberia, S.L. | Millicapsules |
| EP1243690A1 (en) * | 2001-03-22 | 2002-09-25 | Cognis Iberia, S.L. | Process for the antimicrobial finishing of fibres or nonwovens |
| DE10114519A1 (en) * | 2001-03-23 | 2002-10-02 | Haarmann & Reimer Gmbh | Thermally induced release of fragrances or aromas, e.g. for perfuming rooms or objects, using fragrance or aroma immobilized on solid shaped article, e.g. of sugar or ethylene-vinyl acetate copolymer |
| EP1463792B1 (en) | 2001-09-06 | 2008-12-03 | The Procter & Gamble Company | Scented candles |
| AU2002352988A1 (en) * | 2001-11-30 | 2003-06-17 | Bristol-Myers Squibb Company | Pipette configurations and arrays thereof for measuring cellular electrical properties |
| US6753091B2 (en) * | 2001-12-10 | 2004-06-22 | Ming-Jen Huang | Wax decoration items and method making the same |
| EP1348423A1 (en) * | 2002-03-27 | 2003-10-01 | Givaudan SA | Fragrance compositions |
| US7053034B2 (en) * | 2002-04-10 | 2006-05-30 | Salvona, Llc | Targeted controlled delivery compositions activated by changes in pH or salt concentration |
| US7087572B2 (en) | 2002-04-10 | 2006-08-08 | Ecolab Inc. | Fabric treatment compositions and methods for treating fabric in a dryer |
| US7381697B2 (en) | 2002-04-10 | 2008-06-03 | Ecolab Inc. | Fabric softener composition and methods for manufacturing and using |
| US7786069B2 (en) | 2002-04-10 | 2010-08-31 | Ecolab Inc. | Multiple use solid fabric conditioning compositions and treatment in a dryer |
| US20030194416A1 (en) * | 2002-04-15 | 2003-10-16 | Adl Shefer | Moisture triggered release systems comprising aroma ingredients providing fragrance burst in response to moisture |
| US20040175404A1 (en) * | 2002-04-15 | 2004-09-09 | Adi Shefer | Moisture triggered sealed release system |
| GB0208695D0 (en) | 2002-04-16 | 2002-05-29 | Unilever Plc | Fabric treatment composition |
| GB0208696D0 (en) | 2002-04-16 | 2002-05-29 | Unilever Plc | Fabric treatment composition |
| ES2296840T3 (en) * | 2002-04-23 | 2008-05-01 | Cognis Ip Management Gmbh | TENSITIVE PREPARATIONS CONTAINING MICROENCAPSULATED ACTIVE PRODUCTS. |
| US7208460B2 (en) * | 2002-04-26 | 2007-04-24 | Salvona Ip, Llc | Multi component controlled delivery system for soap bars |
| US6740631B2 (en) | 2002-04-26 | 2004-05-25 | Adi Shefer | Multi component controlled delivery system for fabric care products |
| US6825161B2 (en) * | 2002-04-26 | 2004-11-30 | Salvona Llc | Multi component controlled delivery system for soap bars |
| US7316994B2 (en) * | 2002-11-01 | 2008-01-08 | The Procter & Gamble Company | Perfume polymeric particles |
| US8187580B2 (en) * | 2002-11-01 | 2012-05-29 | The Procter & Gamble Company | Polymeric assisted delivery using separate addition |
| US7348024B2 (en) * | 2002-11-17 | 2008-03-25 | Christopher Tararuj | Pull apart fragrance sampler |
| US7670627B2 (en) * | 2002-12-09 | 2010-03-02 | Salvona Ip Llc | pH triggered targeted controlled release systems for the delivery of pharmaceutical active ingredients |
| WO2004058844A1 (en) * | 2002-12-25 | 2004-07-15 | E-Tec Co., Ltd. | Resin particle, resin microcapsule, and methods for producing them |
| US20040224028A1 (en) * | 2003-05-09 | 2004-11-11 | Popplewell Lewis Michael | Polymer particles and methods for their preparation and use |
| DE10333207A1 (en) * | 2003-07-22 | 2005-02-10 | Gerold Tebbe | Method for applying fragrances to textiles and fragrance material |
| US20040224019A1 (en) * | 2004-03-03 | 2004-11-11 | Adi Shefer | Oral controlled release system for targeted drug delivery into the cell and its nucleus for gene therapy, DNA vaccination, and administration of gene based drugs |
| US7279454B2 (en) | 2004-03-18 | 2007-10-09 | Colgate-Palmolive Company | Oil containing starch granules for delivering benefit-additives to a substrate |
| US7276472B2 (en) * | 2004-03-18 | 2007-10-02 | Colgate-Palmolive Company | Oil containing starch granules for delivering benefit-additives to a substrate |
| GB2417204A (en) * | 2004-08-19 | 2006-02-22 | Bell Flavours & Fragrances Ltd | Air treatment apparatus |
| US20080234172A1 (en) * | 2004-11-29 | 2008-09-25 | Givaudan Sa | Substrate Care Product |
| RU2426774C2 (en) * | 2005-09-27 | 2011-08-20 | Дзе Проктер Энд Гэмбл Компани | Detergent composition and preparation methods and use thereof |
| US20070078071A1 (en) * | 2005-09-30 | 2007-04-05 | Kaiping Lee | Spray dry capsule products and methods for preparing and using same |
| US20070179082A1 (en) * | 2006-01-30 | 2007-08-02 | The Procter & Gamble Company | Dryer-added fabric care articles |
| WO2007111887A2 (en) * | 2006-03-22 | 2007-10-04 | The Procter & Gamble Company | Laundry composition |
| DE102006016578A1 (en) * | 2006-04-06 | 2007-10-11 | Henkel Kgaa | Solid textile softening composition with a water-soluble polymer |
| MX2008014213A (en) | 2006-05-05 | 2008-11-14 | Procter & Gamble | Films with microcapsules. |
| US20070270327A1 (en) * | 2006-05-22 | 2007-11-22 | The Procter & Gamble Company | Dryer-added fabric care articles imparting fabric feel benefits |
| WO2007135636A1 (en) * | 2006-05-22 | 2007-11-29 | The Procter & Gamble Company | Dryer-added fabric care articles imparting fabric feel benefits |
| US7659239B2 (en) | 2006-05-24 | 2010-02-09 | The Procter & Gamble Company | Process of incorporating microcapsules into dryer-added fabric care articles |
| US7915215B2 (en) | 2008-10-17 | 2011-03-29 | Appleton Papers Inc. | Fragrance-delivery composition comprising boron and persulfate ion-crosslinked polyvinyl alcohol microcapsules and method of use thereof |
| EP2204155A1 (en) | 2008-12-30 | 2010-07-07 | Takasago International Corporation | Fragrance composition for core shell microcapsules |
| WO2011014641A1 (en) | 2009-07-30 | 2011-02-03 | The Procter & Gamble Company | Fabric conditioning fabric care articles comprising a particulate lubricant agent |
| WO2011046609A2 (en) * | 2009-10-15 | 2011-04-21 | Appleton Papers Inc. | Encapsulation |
| CA2682636C (en) * | 2009-11-05 | 2010-06-15 | The Procter & Gamble Company | Laundry scent additive |
| JP5266547B2 (en) * | 2009-12-25 | 2013-08-21 | ライオン株式会社 | Articles for processing textile products |
| ES2597980T5 (en) | 2010-06-15 | 2020-03-24 | Takasago Perfumery Co Ltd | Core-bark microcapsules containing fragrance |
| MX369325B (en) | 2011-03-18 | 2019-11-05 | Int Flavors & Fragrances Inc | Microcapsules produced from blended sol-gel precursors and method for producing the same. |
| CA2860650C (en) | 2012-01-04 | 2016-08-02 | The Procter & Gamble Company | Active containing fibrous structures with multiple regions |
| US10694917B2 (en) * | 2012-01-04 | 2020-06-30 | The Procter & Gamble Company | Fibrous structures comprising particles and methods for making same |
| FR2985274B1 (en) | 2012-01-04 | 2021-01-08 | Procter & Gamble | FIBROUS STRUCTURES INCLUDING PARTICLES AND THEIR MANUFACTURING PROCESS |
| GB201304667D0 (en) * | 2013-03-15 | 2013-05-01 | Revolymer Ltd | Wax blend polymer encapsulates |
| US10245343B2 (en) * | 2013-08-23 | 2019-04-02 | American Felt & Filter Company | Scented wafer |
| US10221380B2 (en) | 2016-04-01 | 2019-03-05 | The Procter & Gamble Company | Dryer-activated fabric conditioning products having frangible boundaries and methods |
| JP6997171B2 (en) | 2016-08-09 | 2022-01-17 | 高砂香料工業株式会社 | Solid composition containing free fragrances and encapsulated fragrances |
| KR20200086739A (en) | 2018-01-26 | 2020-07-17 | 더 프록터 앤드 갬블 캄파니 | Water soluble unit dose article containing enzyme |
| KR102433420B1 (en) | 2018-01-26 | 2022-08-18 | 더 프록터 앤드 갬블 캄파니 | Water-Soluble Articles and Related Methods |
| US11053466B2 (en) | 2018-01-26 | 2021-07-06 | The Procter & Gamble Company | Water-soluble unit dose articles comprising perfume |
| JP7110356B2 (en) * | 2018-01-26 | 2022-08-01 | ザ プロクター アンド ギャンブル カンパニー | Water soluble unit dose article containing perfume |
| WO2019168829A1 (en) | 2018-02-27 | 2019-09-06 | The Procter & Gamble Company | A consumer product comprising a flat package containing unit dose articles |
| US10982176B2 (en) | 2018-07-27 | 2021-04-20 | The Procter & Gamble Company | Process of laundering fabrics using a water-soluble unit dose article |
| WO2020159860A1 (en) | 2019-01-28 | 2020-08-06 | The Procter & Gamble Company | Recycleable, renewable, or biodegradable package |
| EP3712237A1 (en) | 2019-03-19 | 2020-09-23 | The Procter & Gamble Company | Fibrous water-soluble unit dose articles comprising water-soluble fibrous structures |
| DE102019111837A1 (en) * | 2019-05-07 | 2020-11-12 | Henkel Ag & Co. Kgaa | HEAT / DRYER STABLE PERFUME APPLICATION |
| US20230021841A1 (en) | 2020-02-24 | 2023-01-26 | Firmenich Sa | Sheets Comprising Encapsulated Fragrance Compositions and Methods to Manufacture Same |
| CN112536005B (en) * | 2020-11-05 | 2022-05-03 | 华南理工大学 | Starch-embedded fragrant substance microcapsule and preparation method thereof |
| EP4320305A1 (en) | 2021-06-28 | 2024-02-14 | Firmenich SA | Textile articles for tumble-drying |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2876160A (en) * | 1954-07-26 | 1959-03-03 | Corn Prod Refining Co | Starch matrix material containing imbedded material and process for preparing same |
| US3091567A (en) * | 1961-02-17 | 1963-05-28 | Nat Starch Chem Corp | Encapsulating agents with controlled water repellency |
| US3159585A (en) * | 1961-04-12 | 1964-12-01 | Nat Starch Chem Corp | Method of encapsulating water insoluble oils and product thereof |
| US3455838A (en) * | 1966-04-22 | 1969-07-15 | Nat Starch Chem Corp | Method of encapsulating water-insoluble substances and product thereof |
| US3821436A (en) * | 1971-07-20 | 1974-06-28 | Abbott Lab | Food-flavor-composition |
| US3896033A (en) * | 1972-07-03 | 1975-07-22 | Colgate Palmolive Co | Encapsulated fabric softener |
| US3758323A (en) * | 1972-10-19 | 1973-09-11 | Nat Starch Chem Corp | Dextrin extended gelatin compositions |
| US3971852A (en) * | 1973-06-12 | 1976-07-27 | Polak's Frutal Works, Inc. | Process of encapsulating an oil and product produced thereby |
| JPS5347075B2 (en) * | 1973-07-10 | 1978-12-18 | ||
| US4073996A (en) * | 1976-02-24 | 1978-02-14 | The Procter & Gamble Company | Fabric treating articles and processes |
| GB1567947A (en) * | 1976-07-02 | 1980-05-21 | Unilever Ltd | Esters of quaternised amino-alcohols for treating fabrics |
| GB1587122A (en) * | 1976-10-29 | 1981-04-01 | Procter & Gamble Ltd | Fabric conditioning compositions |
| US4276312A (en) * | 1978-05-25 | 1981-06-30 | Merritt Carleton G | Encapsulation of materials |
| US4511495A (en) * | 1980-05-16 | 1985-04-16 | Lever Brothers Company | Tumble dryer products for depositing perfume |
| US4326967A (en) * | 1980-06-24 | 1982-04-27 | Lever Brothers Company | Liquid formulations for depositing perfumes on fabrics |
| US4446032A (en) * | 1981-08-20 | 1984-05-01 | International Flavors & Fragrances Inc. | Liquid or solid fabric softener composition comprising microencapsulated fragrance suspension and process for preparing same |
| US4536315A (en) * | 1983-06-01 | 1985-08-20 | Colgate Palmolive Co. | Perfume-containing carrier having surface-modified particles for laundry composition |
| GB8520803D0 (en) * | 1985-08-20 | 1985-09-25 | Procter & Gamble | Textile treatment compositions |
| JPH0730512B2 (en) * | 1985-08-22 | 1995-04-05 | ザ、プロクタ−、エンド、ギヤンブル、カンパニ− | Articles and methods for treating fabrics |
| GB2188653A (en) * | 1986-04-02 | 1987-10-07 | Procter & Gamble | Biodegradable fabric softeners |
| US4828746A (en) * | 1986-11-24 | 1989-05-09 | The Procter & Gamble Company | Detergent compatible, dryer released fabric softening/antistatic agents in a sealed pouch |
| US4898680A (en) * | 1986-11-24 | 1990-02-06 | The Proctor & Gamble Company | Detergent compatible, dryer released fabric softening/antistatic agents |
| US4789491A (en) * | 1987-08-07 | 1988-12-06 | The Procter & Gamble Company | Method for preparing biodegradable fabric softening compositions |
| US4911851A (en) * | 1987-11-06 | 1990-03-27 | The Procter & Gamble Company | Detergent compatible, dryer released fabric softening/antistatic agents |
| JPH026672A (en) * | 1988-05-19 | 1990-01-10 | Kanebo Ltd | Persistent perfume-imparting treatment |
| US4954285A (en) * | 1988-03-07 | 1990-09-04 | The Procter & Gamble Company | Perfume, particles, especially for use in dryer released fabric softening/antistatic agents |
| US4842761A (en) * | 1988-03-23 | 1989-06-27 | International Flavors & Fragrances, Inc. | Compositions and methods for controlled release of fragrance-bearing substances |
| US4889643A (en) * | 1988-05-05 | 1989-12-26 | The Procter & Gamble Company | Quench cooled particulate fabric softening composition |
| US4919841A (en) * | 1988-06-06 | 1990-04-24 | Lever Brothers Company | Wax encapsulated actives and emulsion process for their production |
| US5102564A (en) * | 1989-04-12 | 1992-04-07 | The Procter & Gamble Company | Treatment of fabric with perfume/cyclodextrin complexes |
| US4946624A (en) * | 1989-02-27 | 1990-08-07 | The Procter & Gamble Company | Microcapsules containing hydrophobic liquid core |
| CA2009047C (en) * | 1989-02-27 | 1999-06-08 | Daniel Wayne Michael | Microcapsules containing hydrophobic liquid core |
| US5094761A (en) * | 1989-04-12 | 1992-03-10 | The Procter & Gamble Company | Treatment of fabric with perfume/cyclodextrin complexes |
| CA2015737C (en) * | 1989-05-11 | 1995-08-15 | Diane Grob Schmidt | Coated perfume particles |
| GB8917628D0 (en) * | 1989-08-02 | 1989-09-20 | Quest Int | Perfumed fabric softening compositions |
| AU7014991A (en) * | 1990-02-02 | 1991-08-08 | Hercules Incorporated | Carrier composition and method |
-
1991
- 1991-09-25 US US07/766,477 patent/US5246603A/en not_active Expired - Lifetime
-
1992
- 1992-09-21 CA CA002078717A patent/CA2078717C/en not_active Expired - Lifetime
- 1992-09-22 DE DE69227883T patent/DE69227883T2/en not_active Expired - Fee Related
- 1992-09-22 ES ES92308625T patent/ES2124720T3/en not_active Expired - Lifetime
- 1992-09-22 EP EP92308625A patent/EP0539025B1/en not_active Expired - Lifetime
- 1992-09-25 AU AU25357/92A patent/AU664859B2/en not_active Ceased
- 1992-09-25 JP JP4257016A patent/JP2837042B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE69227883D1 (en) | 1999-01-28 |
| EP0539025A2 (en) | 1993-04-28 |
| JPH05222672A (en) | 1993-08-31 |
| JP2837042B2 (en) | 1998-12-14 |
| CA2078717A1 (en) | 1993-03-26 |
| ES2124720T3 (en) | 1999-02-16 |
| DE69227883T2 (en) | 1999-05-12 |
| EP0539025B1 (en) | 1998-12-16 |
| AU664859B2 (en) | 1995-12-07 |
| AU2535792A (en) | 1993-04-01 |
| US5246603A (en) | 1993-09-21 |
| EP0539025A3 (en) | 1994-07-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2078717C (en) | Fragrance microcapsules for fabric conditioning | |
| US5425887A (en) | Encapsualted perfume in fabric conditioning articles | |
| CA2083330C (en) | Fabric conditioning composition containing an emulsified silicone mixture | |
| US6620777B2 (en) | Fabric care composition comprising fabric or skin beneficiating ingredient | |
| AU2005236011B2 (en) | Fabric care composition comprising polymer encapsulated fabric or skin beneficiating ingredient | |
| US6254932B1 (en) | Fabric softener device for in-dryer use | |
| US3686025A (en) | Textile softening agents impregnated into absorbent materials | |
| CA2562011C (en) | Fabric care composition comprising polymer encapsulated fabric or skin beneficiating ingredient | |
| US5300238A (en) | Dryer sheet fabric conditioner containing fabric softener, aminosilicone and bronsted acid compatibilizer | |
| US6956020B2 (en) | Fabric softener compositions | |
| EP1218478B1 (en) | Use of fabric softener compositions | |
| US6133226A (en) | Non-cationic systems for dryer sheets | |
| AU641014B2 (en) | Liquid fabric conditioner and dryer sheet fabric conditioner containing compatible silicones | |
| EP0459821B1 (en) | Liquid fabric conditioner and dryer sheet fabric conditioner containing fabric softener, aminosilicone and bronsted acid compatibiliser | |
| EP1218481B1 (en) | Use of fabric softener compositions | |
| EP0041821A1 (en) | Granular fabric softening composition | |
| CA2002219A1 (en) | Dryer sheet fabric conditioner containing fluorescent whitening agent and method for its preparation | |
| CA1152708A (en) | Granular fabric softening composition | |
| GB2349896A (en) | Delayed release product | |
| IL178380A (en) | Fabric care composition comprising polymer encapsulated fabric or skin beneficiating ingredient |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKEX | Expiry |