Patent Application
20200040281
This invention relates to a fabric care composition which forms a gel or foam exhibiting a crackling sound and/or fizzing.
Aqueous systems containing liquefied gases are known, e.g., in JP2009286734. However, this reference uses larger amounts of liquefied gas and is applied to skin. The reference does not suggest the cleaning composition claimed herein.
The present invention provides a cleaning composition comprising: (a) from 20 to 49 wt % propellant; (b) from 25 to 55 wt % water; (c) from 3 to 12 wt % glycol alkyl ether; (d) from 2 to 12 wt % of an alcohol selected from the group consisting of ethanol and isopropanol; (d) from 1.5 to 5 wt % of a nonionic surfactant; and (e) from 0.3 to 1.5 wt % of a thickener.
Percentages are weight percentages (wt %) and temperatures are in ° C., unless specified otherwise. Operations were performed at room temperature (20-25° C.), unless specified otherwise. Weight percentages of components are based on weights of ingredients as used, e.g., wt % of surfactant is calculated including any water that may be in a commercial surfactant product. Alkyl groups are saturated C1-C20 hydrocarbyl groups which may be straight or branched. Aralkyl groups are substituent groups having an alkyl chain and an aromatic ring (preferably a benzene ring) and which may be attached either through an alkyl carbon or an aryl carbon.
A propellant is a material which is in the vapor phase at 20° C. and atmospheric pressure (101 kPa). Preferably a propellant has a boiling point at atmospheric pressure no lower than −50° C., preferably no lower than −45° C.; preferably no higher than 15° C., preferably no higher than 10° C., preferably no higher than 5° C., preferably no higher than 0° C. Mixtures of propellants may be used. Preferred propellants include alkanes, especially n-butane, propane isobutane, and mixtures thereof. An especially preferred propellant is a mixture of n-butane and propane, preferably in a ratio from 4:1 to 1:4, preferably 3:1 to 1:3, preferably from 2:1 to 1:2. Preferably, the composition comprises at least 23 wt % propellant, preferably at least 26 wt %, preferably at least 30 wt %; preferably no more than 46 wt %, preferably no more than 43 wt %, preferably no more than 40 wt %, preferably no more than 37 wt %.
Preferably a glycol alkyl ether has from six to fifteen carbon atoms; preferably at least seven, preferably at least eight; preferably no more than twelve, preferably no more than eleven, preferably no more than ten. Preferably, a glycol alkyl ether is a mono-alkyl ether. Preferably, a glycol alkyl ether has two or three ethylene oxide (EO) or propylene oxide (PO) units, i.e., molecules of EO or PO which have reacted to form a di- or tri-glycol, preferably two EO or PO units. Numbers of polymerized EO or PO units are number averages. Preferably an alkyl group in a glycol alkyl ether has from two to six carbon atoms; preferably at least three; preferably no more than five, preferably no more than four. Especially preferred alkyl glycol ethers include dipropylene glycol mono-n-propyl ether and dipropylene glycol mono-n-butyl ether. Preferably, the composition comprises at least 4 wt % glycol alkyl ether(s), preferably at least 5 wt %, preferably at least 6 wt %; preferably no more than 11 wt %, preferably no more than 10 wt %, preferably no more than 9.5 wt %.
Preferably, the composition comprises at least 3 wt % of the alcohol, preferably at least 4 wt %, preferably at least 4.5 wt %, preferably at least 5 wt %; preferably no more than 11 wt %, preferably no more than 10 wt %, preferably no more than 9.5 wt %. Preferably, the alcohol is ethanol.
Preferably, nonionic surfactants have an alkyl or aralkyl group having eight to eighteen carbon atoms and three to fifteen polymerized ethylene oxide residues. Preferably nonionic surfactants have an alkyl group rather than an aralkyl group. Preferably, the nonionic surfactant has at least five polymerized ethylene oxide residues, preferably at least seven; preferably no more than twelve, preferably no more than eleven, preferably no more than ten. The number of polymerized ethylene oxide residues is a number average. Preferably, the nonionic surfactant has an alkyl group having at least ten carbon atoms, preferably at least twelve; preferably no more than sixteen, preferably no more than fourteen. Alkyl groups may be mixtures of different chain lengths, e.g., C12-C14. Preferably, alkyl groups are branched. In a preferred embodiment, from one to six polymerized units of propylene oxide are present between the alkyl group and the polymerized ethylene oxide units, preferably from three to five. Preferably, the composition comprises at least 2 wt % nonionic surfactant(s), preferably at least 2.5 wt %, preferably at least 3 wt %; preferably no more than 4.5 wt %, preferably no more than 4 wt %.
Preferably, the thickener is a cellulose ether, alkali swellable emulsion polymer, hydrophobically modified alkali swellable emulsion polymer, hydrophobically modified urethane, guar, gum. Preferably, the thickener is a cellulose ether. Preferably, the cellulose ether is an alkyl ether, a hydroxyalkyl ether or a combination thereof. Preferably, the cellulose ether comprises C1-C4 alkyl and/or hydroxyalkyl groups bonded to hydroxyl oxygen atoms. Preferably, the thickener is hydroxyethyl cellulose. Preferably, the thickener has a viscosity from 500 to 15,000 MPa·s for a 2 wt % aqueous solution, preferably 2,000 to 10,000. Preferably, the composition comprises at least 0.35 wt % thickener(s), preferably at least 4 wt %, preferably at least 0.5 wt %, preferably at least 0.55 wt %; preferably no more than 1.3 wt %, preferably no more than 1 wt %, preferably no more than 0.8 wt %.
Preferably, the composition comprises at least 30 wt % water, preferably at least 35 wt %, preferably at least 40 wt %; preferably no more than 53 wt %, preferably no more than 51 wt %.
The composition may also comprise various other optional ingredients including, without limitation, chelant (e.g., sodium citrate), preservatives (e.g., BHT), salts of fatty acids, anionic surfactant (Sodium Laureth sulfate for instance), hydrogen peroxide; neutralizer (sodium hydroxide, MEA, TEA), enzymes, perfumes
Preferably, the composition is stored under greater than atmospheric pressure in a can. Preferably, the composition is applied to fabric or other inanimate surfaces, and not to skin. This invention is also directed to a method for cleaning fabric by applying the composition to the fabric, preferably at room temperature.
1Dipropylene glycol mono n-propyl ether
2Dipropylene glycol mono n-butyl ether
3Medium molecular weight hydroxyethyl cellulose
4C12-C14 alkyl, 9 moles polymerized ethylene oxide
In a beaker, add the DI water and under mechanical agitation, create a vortex into which the powder CELLOSIZE QP4400H is added slowly. The mixture is hazy.
Wait until the complete hydration of the CELLOSIZE QP4400H (within 3 hours). The mix is then transparent and more viscous.
Add the TERGITOL 15-S-9 (the mix remains transparent), and then the DOWANOL DPnP or DOWANOL DPnB, which generate haziness and decrease the viscosity.
The addition of EtOH will make the formulation transparent again.
The cans are filled with 45 g of the juice. Then, the cans are set with the specific aerosol cap. We fill the aerosol with a n-butane/propane bottle pressurized at 2.5 bars.
If the quantity of gas in the aerosol is not enough, then the aerosols are put in a freezer during 15-20 min.
After this time, we finished the gas filling.
Six dust sebum emulsion (supplied by CFT company-code 020) circular stains have been applied on Cotton (Pillow case, code T13 from Wfk company) with a brush and a stencil so that all the stains have the same surface and shape.
The stains have been stored at room temperature (22° C.) during 2 hours to let them dry. Then, some stains have been treated with either the aerosol formulations A, B or C, by pressing the button during 5 seconds.
After waiting 2 hours, a spatula was used to remove the aerosol formulation/stains system from the surface of the cotton fabric.
The gel system formulation A allows the removal of a bigger amount of stains compared to mousse system formulation B and liquid system formulation C.
The primary cleaning performance test is performed on European washing machines, from Miele, model NOVOTRONIC W1614, set at: 30° C., 30 minutes short program, 1000 rpm, water hardness tuned at 30° TH and loaded with 3.5 kg ballast fabrics.
The primary cleaning performance test is measured after 1 wash cycle on stains on the pillow case cotton code T13 from Wfk Company.
Each washing machine is loaded with ballast fabric and stains, and we add 40 g standard detergent model ECE-2 (no phosphate, for fastness Tests acc/ISO 105-C08/C09 from Testgewee GmbH).
After wash and line dry, each stains are measured in 6 different areas.
We measure the reflectance Y (D65) using a spectrophotometer from Konica Minolta, model CR 2600d. When Y value is high, the stain removal is also high.
We have been able to create some pre spotter aerosols with different textures: crackling gel (formulation A), crackling mousse (formulation B) and crackling liquid (formulation C). Dust sebum emulsion stain pretreated with the formulation A is significantly washed better compared with stains pre-treated with the formulation B and C. The crackling gel system helps in “extracting” the stain out of the fabric, allowing a self-scrubbing effect.
Juice formulation and can filling protocols are identical to example 1.
Dust sebum emulsion (supplied by CFT company-code 020) circular stains have been applied on Cotton (Pillow case, code T13 from Wfk company) with a brush and a stencil so that all the stains have the same surface and shape and same weight: 0.9 g. We applied 9 stains per pillow case and we have 4 replicates per formulation.
The stains have been stored at room temperature (22° C.) during 3 hours to let them dry. Then, some stains have been treated with either the aerosol formulations 1, 2, 3 or 4. Then, the aerosol formulations have been in contact with the stains for 20 minutes.
Then, a spatula was needed to remove the aerosol formulation/stains system from the surface of the cotton fabric.
The primary cleaning performance test is performed on European washing machines, from Miele, model Novotronic W1614, set at: 30° C., 30 minutes short program, 1000 rpm, water hardness tuned at 30° TH and loaded with 3.5 kg ballast fabrics.
The primary cleaning performance test is measured after 1 wash cycle on stains on the pillow case cotton code T13 from Wfk Company.
Each washing machine is loaded with ballast fabric and stains, and we add 40 g standard detergent model ECE-2 (no phosphate, for fastness Tests acc/ISO 105-C08/C09 from Testgewee GmbH).
After wash and line dry, each stains are measured in 6 different areas.
We measure the reflectance Y (D65) using a spectrophotometer from Konica Minolta, model CR 2600d. When Y value is high, the stain removal is also high.
Removing an ingredient from the pre spotter formulation decreases the stain removal performance. This combination of ingredients is relevant.
Juice formulation and can filling protocols are identical to example 1.
Dust sebum emulsion circular stains have been applied on Cotton (Pillow case, code T13 from Wfk company) with a brush and a stencil so that all the stains have the same surface and shape and same weight: 0.4 g. We applied 9 stains per pillow case and we have used 2 replicates per formulation. Stains are left to dry overnight. Two grams of pre spotter formulations are applied on stains and left for 20 minutes.
The stains are not scrubbed and no detergent have been used, to assess pre spotter primary detergency only.
Fabrics are washed once, along with a ballast, using express program at 30° C., 1000 tr/min with no detergent and with a water hardness of 30° TH Fabrics are let to dry out in the darkness and performance is studied through reflectance measurement using a spectrocolorimeter.
Primary cleaning performance increases with the quantity of surfactant added on the pre spotter which is also linked with the visual viscosity and fizzing of the crackling gel.
Primary cleaning performance increases with the quantity of rheology modifier added on the pre spotter, which is also linked with the visual viscosity and fizzing of the crackling gel.
Primary cleaning performance increases when the propellant is present in the pre spotter. Primary cleaning performance is also linked with the visual viscosity and fizzing of the crackling gel.
| Number | Date | Country | Kind |
|---|---|---|---|
| 16290207.6 | Oct 2016 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2017/055510 | 10/6/2017 | WO | 00 |
