Patent Application
20230321302
The present invention relates to volatile composition dispenser for delivering a volatile composition, and particularly relates to solid deodorizers configured for concealing a visual indicator associated with a product life signal.
The use of various devices for diffusion of volatile compounds such as perfumes, sanitizing agents, insect repellants, air freshening compositions, deodorizers are well known. For example, consumers buy air fresheners to freshen their homes. Conventional air fresheners release an air freshening composition into the surroundings for a period of time until the freshening composition is depleted. However, such air fresheners seldom offer adequate visual indication to the consumer that replacement is required before or after the freshening composition is depleted. Accordingly, consumers crave a visual cue that would make it easier to see when it is time for a replacement when the freshening composition in the air freshener is almost finished.
A gel air freshener device that provides a visual cue is described in International Publication No. WO03/008000A1 (Givaudan SA). WO03/008000A1 describes a gel air freshener device that makes use of the shrinkage of the gel matrix to move segments of the device thereby providing a visual cue as to when the gel matrix is exhausted. Specifically, a shaft may be located internally of the device, and appear progressively more prominently as the gel matrix shrinks and the segments close together. However, the gel matrix needs to be opaque so as to hide the shaft before shrinkage of the gel matrix.
In view of the above, there remains a need for an air freshener that can conceal a visual indicator before use.
The present invention relates to a solid deodorizer for concealing a visual indicator associated with a product life signal of the solid deodorizer before use, wherein the solid deodorizer is constructed of a elastomeric polymer material and comprises a volatile composition, wherein the solid deodorizer comprises at least a region characterized by a Haze measurement of at least 40%.
It has been found that end of product life signals in consumer products play an important role in enabling consumers/users to determine when to make a new purchase or to refill the product. In particular, it is difficult for users of volatile dispensing products for delivering a benefit in an interior space to assess whether the volatile composition is exhausted. In particular, for scented volatile compositions, absence of scent may be regarded as an indicator that the perfume is exhausted. However, for non-scented volatile compositions that deliver a benefit without providing a scent (non-scented benefit) such as malodor removal, deodorizing, insect repelling, antibacterial efficacy or the like, physical depletion of the composition is often the only way to indicate end of product usage.
The present invention relates to a solid deodorizer for concealing a visual indicator associated with a product life signal of the solid deodorizer before use, a volatile composition dispenser with a visual product life signal, and a method of providing a visual product life signal for a volatile composition dispenser for delivering a volatile composition in an interior space.
The solid deodorizer is constructed of an elastomeric polymer material and comprises a volatile composition, wherein the solid deodorizer comprises at least a region characterized by a Haze measurement of at least 40%. A technical effect of the Haze measurement on the at least a region of the solid deodorizer is that a visible indicator disposed in or behind the at least a region is less visually perceptible relative to a transparent solid deodorizer having a Haze measurement of less than 40%, for example, 30% or less. Specifically, the Haze measurement of at least 40% causes light rays hitting and reflecting different directions to the eye of the user, thereby resulting in light distortion and rendering the visual indicator not visually perceptible by the human eye. In this way, the visual indicator may be concealed in a variety of ways, before and in use, without requiring complex design of parts in a volatile composition dispenser designed to conceal the visual indicator.
In the following description, the solid deodorizer described hereinafter is a gel composition comprising a perfume as an example of a volatile composition. The gel composition is polyester polyol cross-linked using a cross-linking agent selected from the group consisting of: isocyanates, isothiocynates and mixtures thereof. However, it will be appreciated that the solid deodorizer may be formed from any gel composition that can be molded into three-dimensional objects and that when set, is self-supporting and has at least a peripheral evaporative surface and a central evaporative surface.
The solid deodorizer may be configured in a variety of shapes and sizes to facilitate customization for use as volatile composition dispensers such as air fresheners in vehicles, residential interior spaces, commercial interior spaces, a household furniture interior space such as cupboards or lockers, a household appliance interior space. Preferably the household appliance may be selected from the group consisting of: refrigerators, air conditioners, washing machine, automatic dishwashing machine. The interior space may be a portable consumer product interior environment, preferably the portable consumer product may be bags, luggage or the like.
The solid deodorizer of the present invention can be implemented using a volatile composition dispenser, such as an apparatus for delivering a volatile composition into an interior space. It is contemplated that the apparatus may be configured for use in a variety of applications to deliver volatile materials to the atmosphere and/or a surface as long as the volatile material is evaporated from the apparatus. For the purposes of this disclosure, but without intending to limit the scope of the invention, the apparatus is described as a non-energized apparatus.
For the purposes of illustrating the present invention in detail, the invention is described below as a non-energized volatile composition dispenser. However, the volatile composition dispenser may be configured for use with an energized device such as, for example, an electrical heating device or a fan. In particular, the volatile composition dispenser described is a consumer product, such as an air freshener, for evaporating a volatile composition in spaces to deliver a variety of benefits such as freshening, malodor removal or scenting of air in spaces such as rooms in household and commercial establishments, or enclosed spaces such as a vehicle passenger compartment space. However, it is contemplated that the dispenser may be configured for use in a variety of applications to deliver a volatile composition to the atmosphere and the dispenser may include but is not limited to consumer products, such as, for example air freshening products.
Prior to describing the present invention in detail, the following terms are defined for clarity. Terms not defined should be given their ordinary meaning as understood by a skilled person in the relevant art.
“Vapor release rate” as used herein, refers to a measure of the passage of vapor through a substrate.
Referring to
The volatile composition dispenser 10 further comprises a housing 13 for housing the solid deodorizer 12. The housing 13 may comprise a housing opening 17 configured to enable the at least one central evaporative surface 14 and/or the peripheral evaporative surface 15 to be in fluid communication with an interior space.
The solid deodorizer 12 may be capable of shrinkage from an initial size to a reduced size smaller than the initial size upon exposure of the solid deodorizer 12 to the environment due to vaporization of the volatile composition into the atmosphere of the interior space. The shrinkage of the solid deodorizer in a direction away from the peripheral evaporative surface 15 may be greater than 1% to less than 40%. A visual indicator 18 (shown in
The visual indicator 18 may indicate a state of the dispenser selected from the group consisting of: an end of life of the dispenser, a quantitative state indicative of a number of days use of the dispenser, and combinations thereof. As shown in
The Haze measurement of at least 40% may be applied in the solid deodorizer by applying a surface finish to an entire area of the central evaporative surface 4, 14, such as shown in
To explain the way a solid deodorizer and a visual indicator indicative of a product life signal works to conceal the visual indicator according to the present invention, it is helpful to understand how the visual indicator is concealed in a first configuration and how shrinkage of the solid deodorizer reveals the visual indicator in a second configuration. A method of concealing a visual product life signal for a volatile composition dispenser 20 for delivering a volatile composition in an interior space according to the present invention is described with reference to
Specifically, the present invention relates to a method of concealing a visual product life signal for a volatile composition dispenser for delivering a volatile composition in an interior space, the method comprising:
The solid deodorizer 22 has a length L, width W and thickness D defining a three-dimensional self-supporting structure of the solid deodorizer 12.
The solid deodorizer 22 comprises a volatile composition. The volatile composition may be described as a perfume comprising a mixture of perfume compounds configured to evaporate from the central evaporative surface 24 and/or the peripheral evaporative surface 25. However, it will be appreciated that any volatile composition capable of vaporizing from a solid phase (i.e. in the solid deodorizer 12) to a vapor phase may be employed. The solid deodorizer 22 may further comprise a second central evaporative surface 26 from which the volatile composition may evaporate from upon exposure of the central evaporative surface 26 to the environment.
Further, the volatile composition dispenser 20 comprises a housing 13 for housing the solid deodorizer 22. The volatile composition dispenser 20 is in a substantially vertical orientation. A visual indicator 28 is disposed on an interior of the housing 13 behind the central evaporative surface 24 of the solid deodorizer 22 and proximal to the peripheral evaporative surface 25.
The solid deodorizer 22 may be arranged within the housing 13 such that there is a gap 17 between inner surfaces of the housing and at least a part of the peripheral evaporative surface 25 proximal to the visual indicator 28. The gap 17 may be configured to facilitate air flow in the dispenser so that the peripheral evaporative surface 25 is in fluid communication with air within the housing and the volatile composition can evaporate from the peripheral evaporative surface 25. Specifically, the gap 17 may be configured to enable shrinkage along a first dimension of the solid deodorizer at a faster rate relative to shrinkage along a second dimension of the solid deodorizer. The first dimension may be one of a length, width, thickness of the solid deodorizer, and the second dimension may be the other one of a length, width, thickness of the solid deodorizer. Specifically, the solid deodorizer 22 may be arranged such that there is substantially no gap between an opposite side 26 to the peripheral evaporative surface 25.
A technical effect of texturing is to provide an undulating surface on the at least a region 21 of the central evaporative surface 24. Having an undulating surface causes light rays hitting and reflecting different directions to the eye of the user, thereby resulting in light distortion and rendering the visual indicator not visually perceptible by the human eye.
As shown in
Referring to
A technical effect of a solid deodorizer having a shrinkage of greater than 1% to less than 40% is that a remaining portion of the solid deodorizer 22 has sufficient structure for the solid deodorizer 12 to be a self-supporting structure which does not require a container for supporting the solid deodorizer on a placement surface. Further, it also provides sufficient surface area for ease of removal for users to remove from the placement surface. The placement surface may be a product placement location in the interior space, such as interior surfaces, fixtures, furniture or the like.
The solid deodorizer 22 can be made of an elastomeric polymer material that is capable of providing a self-supporting structure and having a mixture of evaporable ingredients and non-evaporable ingredients, as long as the amounts of the evaporable ingredients and non-evaporable ingredients are configured to provide shrinkage of greater than 1% to less than 40%. Evaporable ingredients may include a volatile composition and water. Non-evaporable ingredients may include ingredients suitable for forming a solid deodorizer including but not limited to gelling materials, elastomers, polyurethane or the like.
Table 1 shows an example of a water-based gel composition according to the present invention.
The solid deodorizer may be non-aqueous, preferably comprises less than 1% by weight of water, more preferably substantially free of water. The solid deodorizer may comprise a material selected from the group consisting of: an ethyl cellulose polymer, a chemically cross-linked polyol or derivative thereof, and mixtures thereof.
Table 2 shows an example of a non-aqueous gel composition comprising an ethyl cellulose polymer which is capable of having a shrinkage of 1% to 40%.
The solid deodorizer may be a chemically cross-linked polyol, wherein the polyol or derivative thereof is selected from the group consisting of: polyol, polyester polyol, polyglycerol and mixtures thereof, preferably the polyol derivative is a polyester polyol, more preferably castor oil, even more preferably the polyester polyol is cross-linked using a cross-linking agent selected from the group consisting of: isocyanates, isothiocynates and mixtures thereof.
The solid deodorizer may also be molded with a moldable material such as any one of the non-aqueous gel compositions described hereinafter.
The gel composition is formed using a cross-linking agent which forms covalent bonds which are stable mechanically and thermally, so once formed are difficult to break. In contrast, physical cross-links rely on changes in the microstructure to achieve stability, such as crystalline regions or regions of high entanglement.
While physical gels can also hold high levels of hydrophobic material such as perfume, the processing of such physical gels is more delicate, as they are more readily broken during manipulation. In addition, such physical gels typically exhibit larger reductions in volume as the hydrophobic material evaporates, in comparison to the cross-linked gels of the present invention, typically at the level of from 50% to 90% by length reduction as the hydrophobic material evaporates. In contrast, the cross-linked gels of the present invention exhibit less shrinkage as the hydrophobic material is released, typically of the order of from 1% to 40%, preferably from 3% to 30%, more preferably from 4% to 20%, at the end of a time period of 1 to 75 days, preferably from 1 to 60 days, more preferably from 1 to 45 days.
The gel can be a chemically cross-linked polyol or derivative thereof. Suitable polyols or derivatives thereof can be selected from the group consisting of: polyol, polyester polyol, polyglycerol, and mixtures thereof. Polyols, polyester polyols and polyglycerols comprise multiple hydroxyl groups, and are suitable for forming gels having a compact network. In addition, the resultant gel has greater affinity for hydrophobic materials which are less strongly hydrophobic.
Suitable polyols or derivatives thereof can have a molecular weight of from 60 Da to 10000 Da, preferably from 150 Da to 3000 Da, even more preferably from 500 Da to 2000 Da, even more preferably 600 Da to 1300 Da. Longer polyols and derivatives thereof, result in greater flexibility of the gel.
Suitable polyols and derivatives thereof do not comprise terminal hydroxyl groups. Secondary alcohols are particularly suitable. Primary alcohols, having terminal hydroxyl groups, typically result in more linear chains and a more compact network. A combination of primary and secondary alcohols are preferred since they result in a more desired correlation length.
A gel with more optimal pore size is achieved when secondary alcohols are used. Lightly branched polyols and derivatives thereof, such as poly(diethyleneglycol adipates) result in more flexible gels. Preferred polyols and derivatives thereof have at least 2 hydroxyl groups per molecule, more preferably at least 3 hydroxyl groups per molecule.
A polyol is a compound containing multiple hydroxyl groups. Diol polyols, having two hydroxyl-functional groups, result after cross-linking in linear polymers or more open networks having large pore size. In contrast, hydroxyl-functional monomers with functionality larger than two form more compact gels with smaller pore sizes. Suitable polyols include: ethylene glycol, propylene glycol, 1,4-butanediol, 1,6-hexanediol, pentaerythritol, 1,2,6-hexanetriol, 4,6-di-tert-butylbenzene-1,2,3-triol, propanetriol (glycerol), 1,2,5-hexanetriol, 1,2,4-cyclohexanetriol, 2,5-dimethylhexane-1,2,6-triol, 3-hydroxymethylpentane-1,2,5-triol, 1,3,6-hexanetriol, 1,1,5,5-pentanetretraol, 1,2,5,6-hexanetretraol, 1,2,3,4,5,6-hexanehexol (sorbitol) and mixtures thereof. Polyester polyols are hydroxyl-containing esters. Suitable polyester polyols can be selected from the group consisting of: aliphatic polyester polyols, aromatic polyester polyols, organic oil based polyester polyols, and mixtures thereof. Organic oil based polyester polyols are preferred. Preferred organic oils are vegetable oils since they typically comprise high levels of unsaturation (C═C bonds) and naturally comprise hydroxyl groups. Suitable polyester polyols include: hexanoic acid, 4-hydroxy-, 1,1′,1″-(1,2,3-propanetriyl) ester; pentanoic acid, 5-amino-4-hydroxy-, 1,1′,1″-(1,2,3-propanetriyl) ester; Polycaprolactone triol; castor oil, hydroxyl sunflower oil (HSO) and mixtures thereof.
Castor oil is particularly suitable. Castor oil (Ricinus oil) is a pale yellow and viscous liquid, derived from the bean of the castor plant (Ricinus communis). Castor oil is predominately made up of triglycerides of fatty acids that contain 87-90% of ricinoleic acid (cis-12-hydroxyoctadec-9-enoic acid) and can be achieved in high purity grades. Castor oil and its derivatives have been used as polyols for polyurethanes and adhesives. The castor oil can be partially hydrogenated. It has been found that castor oil provides the length of the branches and the position of the hydroxyl groups which is particularly suited for providing a chemically cross-linked gel having a pore size which results in slow release of the hydrophobic material, particularly where the hydrophobic material is a perfume. In addition, the chemically cross-linked gels derived from castor oil show less syneresis of the hydrophobic material from the gel.
Polyglycerols are hydroxy-containing ethers. Polyglycerols are typically obtained by the polymerization of alkylene oxides (such as epoxides). Suitable alkylene oxides include ethylene oxide, propylene oxide, butylene oxide, and mixtures thereof, using chain initiators such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, 1,4-butanediol, neopentyl glycol, pentaerythritol, hexanetriol, sorbitol, glycerol, and mixtures thereof. Suitable polyglycerols can be selected from the group consisting of: α,α-diglycerol, α,β-diglycerol, hyperbranched polyglycerol, dendritic polyglycerol, and mixtures thereof. Hyperbranched polyglycerols are aliphatic polyethers with multiple hydroxyl end groups that are obtained from the nonsymmetric polyaddition of glycidol to glycerol resulting in a globular branch-on-branch structure which provides special internal flexibility. Dendritic polyglycerols are a hyperbranched polyglycerol with a well-defined symmetric and spherical three-dimensional structure around a core. Apart from improving gel elasticity, the dendritic structure with sterically shielded core together with the exceptionally high number of functional groups of hyperbranched polyglycerols produces flexible gels with relatively low pore size, which increase the longevity of final composition by reducing the diffusion rate not only as a consequence of physically entrapping the hydrophobic material, but also enhancing H-bonding and Van der Waals interactions. Such polyglycerols can be purchased from Nanopartica GmbH (Germany) and Sigma-Aldrich. Suitable polyglycerols include: polyethylene glycol, polypropylene glycol, poly(diethylene glycol), poly(dipropylene glycol), poly(1,4-butanediol), poly(neopentyl glycol), poly(1,6-hexanediol), and mixtures thereof. The polyglycerol preferably has from 2 to 50, preferably from 4 to 30 repeat units.
Any suitable cross-linking agent can be used, though cross-linking agents selected from the group consisting of: isocyanates, isothiocynates and mixtures thereof, are preferred. The cross-linking agent can be a linear, branched, or cyclic isocyanate, and mixtures thereof. Cyclic isocyanates and mixtures thereof are preferred. Suitable cyclic isocyanates include heterocyclic isocyanates such as 1,3,5-tris(5-isocyanatopentyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione.
Suitable cross-linking agents can be selected from the group consisting of: 1, 4-butane diisocyanate (BDI), 1,6 hexamethylene diisocyanate (HMDI), L-Lysine ethyl ester diisocyanate (LDI), 4,4′-Methylenebis(cyclohexyl isocyanate) (H12MDI), Glycolide-ethylene glycol-Glycolide isocyanate (Bezwada, LLC), 4,4′-Methylenebis(phenyl isocyanate) (MDI), 2,4′-Methylenebis(phenyl isocyanate) (MDI), 2,2′-Methylenebis(phenyl isocyanate) (MDI), Isophorone diisocyanate (IPDI), 2,4-toluene diisocyanate (2,4-TDI), 2,6-toluene diisocyanate (2,6-TDI), Poly (hexamethylene diisocyanate) (PDI), 1,3-bis(2-isocyanatopropan-2-yl)benzene, Poly (pentamethylene diisocyanate) and mixtures thereof, preferably 1,6 hexamethylene diisocyanate (HMDI), L-Lysine ethyl ester diisocyanate (LDI), Poly (pentamethylene diisocyanate), Poly (hexamethylene diisocyanate) (PDI), 1,3,5-tris(5-isocyanatopentyl)-1,3,5-triazine-2,4,6(1H,3H, 5H)-trione, and mixtures thereof. Such cross-linking agents are available from Sigma-Aldrich and from Covestro under trade name of Desmodur® eco N 7300.
The cross-linking agent can have a viscosity below 2.500 mPa·s at 25° C. and an isocyanate equivalent weight of from 15% to 40%, preferably from 18% to 30%. Such cross-linking agents are more easily blended with the polyol. As a result, more uniform gels can be achieved.
The gel is preferably essentially free, or free of unreacted isocyanates and/or isothiocyanates.
The gel can further comprise a hydroxyl containing polymer, a hydroxyl containing oligomer or mixtures thereof. The hydroxyl containing polymer and/or oligomer can be used to alter the elasticity of the gel composition, and therefore the longevity of the perfume release. since a higher elastic modulus G′ slows the perfume release.
Suitable hydroxyl containing polymers can be selected from the group consisting of: poloxamers, gelatins, carrageenan, chitin, chitosan, and mixtures thereof.
Poloxamers are nonionic triblock copolymers composed of a central hydrophobic chain of polyoxypropylene (poly(propylene oxide)) flanked by two hydrophilic chains of polyoxyethylene (poly(ethylene oxide)). Suitable poloxamers have a weight average molecular weight of from 1500 g/mol to 15000 g/mol and a poly(ethylene oxide) weight percentage of from 10% to 80%, preferably from 50% to 80%. Suitable poloxamers are commercially available under the tradename of Pluronic® from BASF.
Gelatins are typically translucent, colorless, and typically obtained from collagen from various animal body parts. They are commonly used as a gelling agent in food, pharmaceutical industry, vitamin capsules, photography, and cosmetic manufacturing. Suitable gelatines can have a bloom of from 90 to 300. Bloom is a test to measure the strength of a gel or gelatin and is measured according to the method outlined by Bloom in U.S. Pat. No. 1,540,979. The test determines the weight in grams needed by a plunger with a diameter of 0.5 inch (12.7 mm) to depress the surface of the gel 4 mm without breaking it, at a temperature of 25° C. The result is expressed in Bloom (grades). It is usually between 30 and 300 Bloom. To perform the Bloom test on gelatin, a 6.67% by weight gelatin solution is kept for 17-18 hours at 10° C. prior to being tested.
Carrageenan are sulfated polysaccharide for instance derived from red algae, commonly known as Irish moss. They are typically composed principally of alpha-D-galactopyranose-4-sulfate units and 3,6-anhydro-alpha-D-galactopyranose units. At least three forms are known, designated, respectively, as “iota”, “kappa” and “lambda” carrageenan which differ in the ratios of the two galactopyranose units and accordingly in their sulfate ester content.
Kappa-carrageenan is the principal component in aqueous extracts from Chondrus crispus and Gigartina stellata. It is lower in sulfate ester content than iota and lambda carrageenan.
Chitosan is typically obtained by deacetylation under alkaline conditions of chitin, which is the second most abundant biopolymer in nature, after cellulose. Chitin can be found as an important constituent of the exoskeleton in animals, especially in crustaceans, molluscs and insects, and it is also the principal polymer in the cell wall of certain fungi. Chitin and chitosan are linear polysaccharides composed of randomly distributed β-(1-4)-linked D-glucosamine (deacetylated unit) and N-acetyl-D-glucosamine (acetylated unit). Chitosan has two types of reactive groups that can be grafted: the free amine groups on the deacetylated units and the hydroxyl groups on the C3 and C6 carbons on acetylated or deacetylated units.
The chitosan of the present invention may have a molecular weight from 10,000 g/mol to 4,000,000 g/mol, preferably from 70,000 g/mol to 1,600,000 g/mol. Suitable chitosan may have a degree of de-acetylation of at least 50%, preferably at least 60%, more preferably at least 70%, even more preferably at least 75%.
The gel composition can be transparent or even translucent. The gel composition can have any suitable shape, such as star, circular or pyramidal. The gel composition may be colored by adding dye. The gel compositions of the present invention can be molded or even 3D printed to the desired shape.
The gel composition can be any suitable shape or size, since both define the evaporative surface area of the gel composition. It is known that the shape and size of the gel composition can affect the release and longevity of the hydrophobic material. For instance, thin sheets result in faster release and lower longevity than spheres of the same mass of the gel composition. Suitable gel compositions can have an evaporative surface area of less than 150 cm2, preferably from 3.0 to 100 cm2, more preferably from 6.0 to 60 cm2.
The evaporative surface area can be measured by creating a 3D model of the gel composition using CAD software and using the CAD software to calculate the surface area. Any suitable CAD software can be used, such as AutoCAD® 2013.
The total surface area of the first and second central evaporative surfaces 4 and 6 may be from 100 mm2 to 10000 mm2, from 1000 mm2 to 8000 mm2, from 1500 mm2 to 6000 mm2, from 2000 mm2 to 4000 mm2, or different combinations of the upper and lower values described above or combinations of any integer in the ranges listed above. The solid deodorizer may be in a form selected from the group consisting of: a tablet, a sheet, a film and combinations thereof, preferably the deodorizer is a tablet comprising a shape selected from the group consisting of: a polygon shape, a circular shape, a non-polygon shape including a curve, a non-polygon shape with an open end and combinations thereof.
The deodorizer may be characterized by a volume of greater than 2 cm3.
The deodorizer may further comprise a first central evaporative surface, a second central evaporative surface and a peripheral evaporative surface between the first and second central evaporative surfaces, wherein each of the first and second central evaporative surfaces is characterized by an evaporative surface area greater than 2 cm2, preferably from 3 cm2 to 150 cm2.
The housing, front cover, rear cover, and the article holder may be made of plastic, paper, or any material chemically compatible with the solid deodorizer.
The volatile composition dispenser descried hereinbefore may be configured in any orientation, such as in a vertical orientation during use such as shown in
The following examples are intended to more fully illustrate the present invention and are not to be construed as limitations of the present invention since many variations thereof are possible without departing from the scope of the present invention. All parts, percentages and ratios used herein are expressed as percent weight unless otherwise specified.
Inventive Samples of solid deodorizers made with the composition details described in the following tables and according to the process described below.
The polyol or derivative thereof, is mixed with the volatile composition, and optionally a hydroxyl containing polymer is added. Then, the cross-linking agent is added at a temperature from 5° C. to 35° C., preferably 15° C. to 30° C. and further mixed in order to provide a homogeneous mixture. The mixture is poured into a mould of the desired shape, and cured, preferably at a curing temperature from 20° C. to 30° C. Such temperatures limit the evaporation of volatile components of the hydrophobic material. Alternatively, the mixture can be kept at 5° C. or less, in order to avoid curing. Curing will then start only once the temperature is raised to the curing temperature.
The polyol or derivative thereof can be mixed with the cross-linking agent, and optionally a hydroxyl containing polymer, preferably at a temperature from 20° C. to 85° C., more preferably from 30° C. to 75° C., for 10 min to 10 hours, preferably from 15 min to 2 hours. The mixture is cooled down and the hydrophobic material is added preferably at a temperature from 10° C. to 40° C., more preferably 15° C. to 30° C. and can be further mixed, for instance, from 15 to 120 min. The mixture is poured into the desired mould and cured, preferably at a temperature from 20° C. to 30° C.
Alternatively, all of the components of the gel composition can be blended at a low temperature, such as 5° C. or less, before the temperature is increased to the curing temperature.
Solid deodorizers according to the present invention are prepared based on the composition details described in Table 3 below and according to the process described hereinbefore. The solid deodorizers are evaluated for the visual perceptibility of the visual indicator in the first configuration (results shown in Table 4).
Expert panel is consulted for the visual check shown in Table 4.
The total transmission, diffuse transmission, and haze measurements for each of the Comparative and Inventive Samples are measured according to the ASTM 01003-13 test method for Haze with PerkinElmer Lambda 950 UV/VIS/NIR spectrophotometer (with 150 mm integrating sphere) instrument. A low Haze measurement value corresponds to a clarity of the solid deodorizer.
Specifically, Haze is determined by the following equation:
Haze=Diffuse Transmission/(Total Transmission(specular and diffuse transmission))*100%
Data is provided demonstrating the volatile composition dispenser of the present invention having a visible indicator for providing a visual product life signal. Solid deodorizers according to the present invention are prepared based on the composition details described in Table 5 below and are evaluated for the respective shrinkage (results shown in Table 5). Each of the inventive samples comprise
Shrinkage results of the Inventive Samples 1 to 6 of Table 5 are shown in Table 6 below. Specifically, the shrinkage is determined based on Formula (1) below:
Shrinkage=(Initial Length−Reduced Length)/Initial Length×100%
wherein,
Initial Length=length or diameter of the solid deodorizer before use
Reduced Length=length or diameter of the solid deodorizer after a predetermined time period of use.
All the above Inventive Samples 1 to 6 have a shrinkage of 6.3% to 12.5%, i.e. less than 40%. As a result, each of the samples at the end of life is a single unitary piece having a size sufficient for easy removal and thereby reducing mess. In contrast, conventional gels have a gelling polymer which remains after water and perfume evaporates, and the remaining gelling polymer causes stickiness in the gel. Further, the remaining gel also stick to the container break easily and causes messy residue.
An example is described:
The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm.”
Every document cited herein, including any cross referenced or related patent or application and any patent application or patent to which this application claims priority or benefit thereof, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests, or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.
While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.
| Number | Date | Country | |
|---|---|---|---|
| 63329482 | Apr 2022 | US |
