EP0182583B1 - Verfahren zum Reinigen von Textilien mit cyclischen Siloxanen - Google Patents

Verfahren zum Reinigen von Textilien mit cyclischen Siloxanen Download PDF

Info

Publication number
EP0182583B1
EP0182583B1 EP19850308214 EP85308214A EP0182583B1 EP 0182583 B1 EP0182583 B1 EP 0182583B1 EP 19850308214 EP19850308214 EP 19850308214 EP 85308214 A EP85308214 A EP 85308214A EP 0182583 B1 EP0182583 B1 EP 0182583B1
Authority
EP
European Patent Office
Prior art keywords
cleaning
cyclic
percent
stain
weight
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
Application number
EP19850308214
Other languages
English (en)
French (fr)
Other versions
EP0182583A2 (de
EP0182583A3 (en
Inventor
Kenneth Alfred Kasprzak
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Silicones Corp
Original Assignee
Dow Corning Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dow Corning Corp filed Critical Dow Corning Corp
Publication of EP0182583A2 publication Critical patent/EP0182583A2/de
Publication of EP0182583A3 publication Critical patent/EP0182583A3/en
Application granted granted Critical
Publication of EP0182583B1 publication Critical patent/EP0182583B1/de
Expired legal-status Critical Current

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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/162—Organic compounds containing Si

Definitions

  • the present invention relates to a method for removing soil from textiles using cyclic dimethylpolysiloxanes.
  • this invention relates to the use of cyclic dimethylpolysiloxanes for removal of oily/greasy stains from textiles.
  • Textile products such as fabrics, carpets and upholstery often develop prominent stain spots from inadvertent contact with foodstuff and other materials containing grease and oils.
  • Various organic solvents such as alcohols, petroleum hydrocarbons, and chlorinated hydrocarbons have been used in cleaning compositions adapted for direct application to fabric as spot removers.
  • nonresidue cleaners are formulated with volatile components only. After dissolving, mobilizing, and removing the stained material, such formulations are intended to completely evaporate leaving no residue components on the textile.
  • Other cleaning compositions employ a combination of solvent and solid, absorbent particles. The solvent mobilizes the soil and the absorbent solid attracts the soil and solvent to itself. The residue of absorbent solid is intended to be easily removed from the textile by brushing or vacuuming.
  • Yet another approach involves liquid detergent compositions which have been adapted as prewash spot removers. These compositions usually contain concentrated synthetic surfactants with alcohol or other solvents.
  • the prewash spot remover composition When used as a prewash spot remover, the nonvolatile surfactant components remain on the textile as a residue which is removed by a conventional home laundry operation.
  • the prewash spot remover composition additionally functions in the manner of a heavy-duty laundry detergent.
  • Stain removing compositions are disclosed in Japanese Patent Publication Kokai No. (1974)-35681, which contain small amounts (0.5 to 10 weight percent) of silicone oil combined with cleaning solvents such as trichlorethane and petroleum hydrocarbons. Although the type of silicone oil employed is not further identified, it is taught that the silicone remains on the fabric after cleaning to provide continuing water repellency and soil resistance for the fabric. Consequently, it is apparent that this publication does not contemplate the use of completely volatile cyclic dimethylpolysiloxanes.
  • An aerosol type aqueous cleaning composition is disclosed in Japanese Patent Publication Kokai No. (1978)-56203, which contains nonionic surfactant, alkanolamine, glycol ether, alcohol, propellant, and 0.02 to 0.1 weight percent of linear dimethylpolysiloxane with 2 to 7 silicon atoms per molecule.
  • This publication discloses only the use of very low amounts of linear dimethylpolysiloxanes and does not contemplate the use of larger, solvent-effective amounts of the cyclic dimethylpolysiloxanes.
  • tetraethoxysilane as a solvent for removing grease from textiles is disclosed in Russian Patent Publication 979548-A.
  • tetraethoxysilane is not stable in contact with water and may hydrolyze forming alcohol and silica solids.
  • Liquid cleaning compositions for removing dirt and grit from solid surfaces are disclosed in U.S. Patent No. 2,955,047.
  • the compositions contain surfactants, water, water-miscible organic solvent, and an oil-in-water emulsion of dimethylpolysiloxane oil.
  • the siloxane polymer is said to impart a high glossy polish to the treated surfaces by depositing a monomolecular film on the surface.
  • U.S. Patent No. 2,993,866 teaches an aerosol glass cleaner composition containing isopropanol, fluorochlorohydrocarbon propellants, and linear dimethylpolysiloxane having a viscosity of about 200 centistokes.
  • An all purpose cleaner composition containing a mixture of surfactants, isopropyl alcohol, and a silicone defoaming agent is disclosed in U.S. Patent No. 4,311,608.
  • the silicone defoaming agent is an oil-in-water emulsion of dimethylsiloxane polymer.
  • a cleaner (apparently a wiper type) impregnated with a composition containing mineral oils or alcohols with organopolysiloxanes is disclosed in Japanese Patent Publication Kokai No. (1975)-161059.
  • the organopolysiloxanes are characterized by having a viscosity of not more than 30 centipoise at 20°C.
  • This invention provides a method for cleaning textiles which comprises applying in the absence of water a non-aqueous liquid composition containing 1 to 100 percent by weight of a cyclic siloxane selected from octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexasiloxane to a textile soiled with oil, grease or sebum, and removing from the textile a combination comprising cyclic siloxane and oil, grease or sebum.
  • a cyclic siloxane selected from octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexasiloxane
  • the novel textile cleaning compositions are applied to a soiled area of clothing, carpet, or other textile by spraying, pouring, or from a cloth or sponge applicator.
  • the composition may be rubbed or brushed into the textile to facilitate loosening and dissolving the soil components.
  • the soil-solvent combination is then removed from the textile by any of the well known methods such as blotting with absorbent material, absorption unto particulate material followed by vacuuming, or a conventional home laundry operation.
  • cyclic siloxanes employed in the liquid cleaning and spot removing compositions of this invention are available commercially and are made by well known methods such as, for example, the hydrolysis and condensation of dimethyldichlorosilane.
  • cyclic siloxanes employed according to this invention are relatively volatile materials having boiling points below about 250°C at 760 mm Hg.
  • a single cyclic siloxane may be used in the liquid cleaning composition or any mixture of two or more of the cyclic siloxanes may be used.
  • Specifically preferred cyclic siloxanes for use in this invention are octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexasiloxane.
  • useful cyclic siloxane mixtures may contain, in addition to the preferred cyclic siloxanes, minor amounts of other cyclic siloxanes including hexamethylcyclotrisiloxane or higher cyclics such as tetradecamethylcycloheptasiloxane. Generally the amount of these other cyclic siloxanes in useful cyclic siloxane mixtures will be less than about 10 percent based on the total weight of the mixture.
  • the amount of cyclic siloxane used in the liquid cleaning compositions of this invention is not critical so long as the amount used is effective to aid soil removal from textiles.
  • the cleaning composition may contain, for example, from 1 to 100 percent by weight of the cyclic siloxanes. It is preferred that the cleaning composition contain from 5 to 100, or more preferably 10 to 100, percent by weight of the cyclic siloxanes.
  • liquid cleaning compositions of this invention may be included in the liquid cleaning compositions of this invention such as conventional cleaning solvents, absorbent solid particulate materials, synthetic builders, water soluble organic detergent compounds, and cationic antistatic substances.
  • nonresidue spot cleaning compositions may contain conventional cleaning solvents mixed with cyclic siloxanes according to the present invention.
  • Any conventional cleaning solvent having a boiling point below about 250°C can be mixed with the cyclic siloxanes to prepare a liquid composition useful in the present invention.
  • Useful additional cleaning solvents include alcohols such as isopropanol and butanol, petroleum hydrocarbons such as mineral spirits, and chlorinated hydrocarbons such as methylene dichloride, tetrachloroethylene, and trichloroethylene.
  • Mixtures of cyclic siloxanes and conventional solvents selected from the group consisting of petroleum hydrocarbons and chlorinated hydrocarbons are especially effective. Mixtures containing about 30 to 70 percent by weight of conventional cleaning solvent and 30 to 70 percent by weight of the cyclic siloxane are preferred because of their superior ability to mobilize stains.
  • Cleaning compositions of the solvent/absorbent class are also useful in the method of this invention.
  • Such cleaning compositions may contain in addition to the cyclic siloxane any of the absorbent materials known for such applications.
  • Useful absorbent materials include mineral particulates such as silica, talc, diatomaceous earth, kaolinite; organic particulates such as starch and modified starch, nut shell flour, and ground rice hulls; and synthetic porous polymers such as the urea-formaldehyde polymer particles described in U.S. Patent No. 3,910,848, which more fully describes the polymer particles.
  • the absorbent material is generally used in amounts of about 5 to 40 percent based on the weight of cleaning solvent in the composition.
  • Cleaning compositions of the solvent/absorbent class may also include a cationic antistatic agent to facilitate the removal of the particulate material during brushing or vacuuming of the textile material.
  • a cationic antistatic agent to facilitate the removal of the particulate material during brushing or vacuuming of the textile material.
  • Useful cationic antistats include quaternary nitrogen salts that contain at least one C10 to C24 aliphatic hydrocarbon substituent on the nitrogen such as stearyltrimethylammonium chloride.
  • Antistatic agents are typically employed in amounts of about 0.1 to 3 percent by weight based on the total weight of the cleaning composition.
  • the method for cleaning textiles of this invention also includes the use of prewash spot remover compositions containing nonvolatile surfactant components in addition to cyclic siloxane solvent.
  • Such prewash spot remover compositions will generally include a water soluble organic detergent material and synthetic builders in combination with the cyclic siloxane solvent.
  • Detergent compounds useful in prewash spot removers are the anionic, nonionic, zwitterionic and ampholytic surfactant compounds.
  • Such detergent compounds are well known to those skilled in the detergent art. Exemplary detergents are described in the well-known books entitled "Surface Active Agents" by Schwartz and Perry and “Surface Active Agents and Detergents” by Schwartz, Perry and Berch, both by Interscience Publishers, New York, N.Y.
  • nonionic surfactants which are condensation products of polyethylene oxide with an organic hydrophobic compound which is usually aliphatic or alkylaromatic in nature.
  • exemplary nonionic surfactants are polyethylene oxide condensates of nonyl phenol and polyethylene oxide condensates of myristyl alcohol.
  • prewash spot removing compositions of this invention from about 10 to 80 percent by weight of surfactants may be used in the prewash spot removing compositions of this invention. More preferred prewash spot removing compositions contain 30 to 70 percent by weight of nonionic surfactants.
  • Prewash spot removers of this invention may also contain a variety of builder compounds such as sodium tripolyphosphate, sodium carbonate, sodium silicate, the alkali metal, ammonium and substituted ammonium salts of oxydisuccinic acid, oxydiacetic acid, carboxymethyloxymalonic acid, carboxymethyloxysuccinic acid, lactoxysuccinic acid, citric acid, mellitic acid, tetrahydrofurantetracarboxylic acid, polyacrylic acid, nitrilotriacetic acid, oxidized starches and mixtures thereof.
  • Builders are generally added to prewash spot removing compositions in amounts ranging from 0 to about 50 percent by weight based on the weight of the total composition.
  • the liquid compositions of the present invention are especially adapted for direct application to stains and soils on fabrics and other textiles.
  • the compositions can be applied to soiled textiles by any of the commonly used methods.
  • the liquid compositions may be poured or sprayed onto the stains.
  • the composition may be brushed or rubbed onto the stained or soiled area using absorbent items such as brushes, paper towels, cloth or sponges that contain the cleaning composition.
  • the cyclic siloxane acts to dissolve and/or loosen the soil which it contacts.
  • the mobilized soil is then more easily removed from the textile in combination with the cyclic siloxane.
  • the cyclic siloxane/soil combination can be removed from the textile by any convenient method such as blotting the textile with a dry absorbent material.
  • the textile may be blotted, for example, with sponges, paper towels, or cloth towels.
  • the soil/cyclic siloxane combination may be removed by processes such as brushing, vacuuming, or conventional home laundry operations. Brushing and vacuuming are especially useful if solid, absorbent particles are employed in the liquid cleaning composition.
  • Conventional home laundry is the preferred method of removal when nonvolatile surfactants are used in combination with cyclic siloxane in the cleaning composition.
  • cyclic siloxanes are sufficiently volatile that any residual cyclic siloxane on the textile, after removal of the soil, readily volatilizes to leave the treated area dry as well as clean.
  • the method of the present invention can be used to remove a wide variety of soils and stains.
  • the cyclic siloxane is especially effective at removing oil and grease spots or stains.
  • One special advantage of the cyclic siloxanes as cleaning solvents is that the formation of a secondary stain ring is either eliminated or greatly reduced in definition.
  • Another advantage is that the cyclic siloxanes are essentially nontoxic and nonharmful in the environment.
  • cyclic siloxanes can be used with a wide variety of fabrics without harming or in any way changing the appearance of the fabric.
  • the method of cleaning of this invention can be used on all types of textiles including carpets and fabrics used for clothing or upholstery.
  • Artificial sebum employed in the following examples was prepared from a base mixture of palmitic acid (5 g), stearic acid (2.5 g), coconut oil (7.5 g), paraffin (5 g), spermaceti (7.5 g), olive oil (10 g), squalene (2.5 g), cholesterol (2.5 g), oleic acid (5 g), and linoleic acid (2.5 g).
  • a melted 49°C (120°F) 5 g portion of the base mixture was combined with oleic acid (4 g) and triethanolamine (8 g) and agitated at 49°C (120°F) until homogenous.
  • air filter dirt (12 g, +200 mesh) and deionized water (100 ml) were added and the mixture agitated for ten minutes. Additional deionized water (900 ml) was added and the mixture was agitated in a homogenizer for ten minutes. The mixture was stored in a 38°C (100°F) oven and shaken well before using for staining.
  • Cotton fabric test pieces were prepared with approximately 2.5cm (1 inch) diameter stains of used motor oil, cooking oil and artificial sebum. The stains were aged at room temperature for 24 hours. Stains were cleaned by placing the fabric pieces on several absorbent paper towels and rubbing the stained area for 20 seconds with a paper towel saturated with the cleaning fluid.
  • the cyclic siloxane fluids tested were (A) octamethylcyclotetrasiloxane, (B) decamethylcyclopentasiloxane, (C) a cyclic siloxane mixture of about 91 percent by weight octamethylcyclotetrasiloxane and about 8 percent by weight decamethylcyclopentasiloxane, and (D) a cyclic siloxane mixture of about 1.3 percent by weight octamethylcyclotetrasiloxane, about 69.3 percent by weight decamethylcyclopentasiloxane and about 29.1 percent by weight dodecamethylcyclohexasiloxane.
  • hexamethyldisiloxane, mineral spirits, tetrachloroethylene, isopropyl alcohol, and xylene were also used to clean the stains.
  • the ratings were made by comparison of the test pieces with a standard series of exemplary stains in a black box using a fluorescent light source. Deviations between the test pieces and the standard stains are indicated by fractional ratings.
  • the used motor oil tended to form a dual stain containing a smaller sludge portion nearer the center and a larger oil portion which spread out more from the point of application.
  • Example 2 The stain removal testing procedure of Example 1 was repeated using a 65/35 polyester/cotton fabric. The results of the black box visual ratings of the cleaned fabric are presented in Table 2.
  • Example 3 The stain removal testing procedure of Example 1 was repeated using a 100 percent polyester fabric. The results of the black box visual ratings of the cleaned fabric are presented in Table 3.
  • Example 1 The stain removal testing procedure of Example 1 was modified by heat setting the stain before cleaning. Stains were set by placing the fabric in an automatic clothes dryer at the high temperature setting for two cycles of 60 minutes each. Polyester (100%) fabric was used in these tests. Results of the black box visual ratings of cleaned fabric are presented in Table 4.
  • the following experiments demonstrate the relative efficiency of cyclic dimethylpolysiloxanes in spreading oil stains on fabric.
  • the degree of spreading of the stain relates to the extent of mobilization of the stain by the solvent being tested. Generally, the more effectively a stain can be mobilized, the more easily and completely it can be removed from the fabric.
  • Cotton fabric test pieces (20cm x 20cm) (8 inch x 8 inch) were placed in an embroidery hoop and approximately 1 ml of cooking oil was applied to the center of the fabric. Stains were aged at room temperature for 24 hours. The fabric was then positioned under a burette filled with the cleaning fluid. With the burette tip just above the center of the stain, a 0.5 ml portion of the cleaning fluid was dropped on the stain. The fabric was allowed to dry at room temperature and the size of the resulting stain was measured. Generally the stains were circular or slightly oval in shape. The approximate areas of the stains after the spreading process with various cleaning fluids are shown in Table 5. In the case of oval shaped stains, approximate areas were calculated as if the stain were circular using a diameter equal to the average of the length and width of the oval. The cyclic siloxane fluids tested are described in Example 1.
  • Example 5 The stain spreading procedure of Example 5 was repeated using 100% polyester fabric test pieces. The approximate stain areas after spreading are shown in Table 6.
  • Example 7 The stain spreading procedure of Example 5 was repeated using a 65/35 polyester/cotton fabric. Approximate stain areas after spreading are presented in Table 7.
  • Cooking oil stains were prepared on 65/35 polyester/cotton fabric and the spreading procedure of Example 5 was repeated except that a 1 ml portion of a blend of cleaning materials was dropped on the stain.
  • Octamethylcyclotetrasiloxane was blended in various proportions by weight with either mineral spirits or tetrachloroethylene to prepare the cleaning materials.
  • the approximate stain areas after spreading are shown in Table 8.
  • Example 8 The stain spreading procedure of Example 8 was repeated using decamethylcyclopentasiloxane blended in various proportions by weight with either mineral spirits or tetrachloroethylene. The approximate stain areas after spreading are presented in Table 9.
  • Polyester fabric test pieces were prepared with approximately 2.5cm (1 inch) diameter stains of used motor oil, cooking oil, and artificial sebum. Stains were heat set by placing the fabric in an automatic clothes dryer at the high temperature setting for two cycles of 60 minutes each. Each stain was treated with 2 ml of the test fluid as described in Example 1. Each fluid was left on the stain for one to two minutes. The test fabric pieces were then washed in a household automatic washer on the normal setting using the recommended level of a powdered nonphosphate detergent. The fabric pieces were dried in an automatic clothes dryer on the permanent press setting.
  • the used motor oil tended to form a dual stain containing a smaller sludge portion nearer the center and a larger oil portion which spread out more from the point of application. Some differences in the cleaning of the two portions of these stains were observed and consequently the cleaning of each portion was separately rated. The results of the visual rating are presented in Table 10.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Claims (7)

  1. Verfahren zum Reinigen von Textilien,
    gekennzeichnet durch
    Aufbringen, in Abwesenheit von Wasser, einer nicht wäßrigen flüssigen Zusammensetzung, enthaltend 1 bis 100 Gew.-% eines zyklischen Siloxans, ausgewählt aus Octamethylcyclotetrasiloxan, Decamethylcylclopentasiloxan und Dodecamethylcyclohexasiloxan auf eine mit Öl, Fett oder Talg verschmutzte Textilie und Entfernen einer Kombination, enthaltend zyklisches Siloxan und Öl, Fett oder Talg, aus der Textilie.
  2. Verfahren nach Anspruch 1,
    dadurch gekennzeichnet,
    daß die flüssige Zusammensetzung 5 bis 100 Gew.-% zyklische Siloxane enthält.
  3. Verfahren nach Anspruch 2,
    dadurch gekennzeichnet,
    daß die flüssige Zusammensetzung 10 bis 100 Gew.-% zyklische Siloxane enthält.
  4. Verfahren nach Anspruch 3,
    dadurch gekennzeichnet,
    daß die flüssige Zusammensetzung 30 bis 70 Gew.-% zyklisches Siloxan und 30 bis 70 Gew.-% eines aus Benzinkohlenwasserstoff und chlorierten Kohlenwasserstoffen ausgewählten Reinigungslösemittels enthält.
  5. Verfahren nach Anspruch 4,
    dadurch gekennzeichnet,
    daß die flüssige Zusammensetzung zyklisches Siloxan und Waschbenzin enthält.
  6. Verfahren nach Anspruch 4,
    dadurch gekennzeichnet,
    daß die flüssige Zusammensetzung zyklische Siloxane und einen chlorierten Kohlenwasserstoff als Reinigungslösemittel enthält.
  7. Verfahren nach Anspruch 6,
    dadurch gekennzeichnet,
    daß die flüssige Zusammensetzung zyklisches Siloxan und Tetrachlorethylen enthält.
EP19850308214 1984-11-13 1985-11-12 Verfahren zum Reinigen von Textilien mit cyclischen Siloxanen Expired EP0182583B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US67019584A 1984-11-13 1984-11-13
US670195 1984-11-13

Publications (3)

Publication Number Publication Date
EP0182583A2 EP0182583A2 (de) 1986-05-28
EP0182583A3 EP0182583A3 (en) 1988-04-06
EP0182583B1 true EP0182583B1 (de) 1991-07-03

Family

ID=24689398

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19850308214 Expired EP0182583B1 (de) 1984-11-13 1985-11-12 Verfahren zum Reinigen von Textilien mit cyclischen Siloxanen

Country Status (5)

Country Link
EP (1) EP0182583B1 (de)
JP (1) JPS61119765A (de)
AU (1) AU585906B2 (de)
CA (1) CA1239326A (de)
DE (1) DE3583377D1 (de)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7695524B2 (en) 2003-10-31 2010-04-13 Whirlpool Corporation Non-aqueous washing machine and methods
US7739891B2 (en) 2003-10-31 2010-06-22 Whirlpool Corporation Fabric laundering apparatus adapted for using a select rinse fluid
US7837741B2 (en) 2004-04-29 2010-11-23 Whirlpool Corporation Dry cleaning method
US7966684B2 (en) 2005-05-23 2011-06-28 Whirlpool Corporation Methods and apparatus to accelerate the drying of aqueous working fluids
US8262741B2 (en) 1997-04-29 2012-09-11 Whirlpool Corporation Non-aqueous washing apparatus and method

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY107434A (en) * 1989-10-26 1995-12-30 Momentive Performance Mat Jp Cleaning compositions.
DE3940804A1 (de) * 1989-12-09 1991-06-13 Kreussler Chem Fab Verwendung von cyclosiloxanen, isoparaffinen und/oder testbenzinen
GB9002716D0 (en) * 1990-02-07 1990-04-04 Dow Corning Sa Method of bonding silicone elastomer to a substrate
US5503681A (en) * 1990-03-16 1996-04-02 Kabushiki Kaisha Toshiba Method of cleaning an object
US5593507A (en) * 1990-08-22 1997-01-14 Kabushiki Kaisha Toshiba Cleaning method and cleaning apparatus
DE69330664T2 (de) * 1992-01-21 2002-07-04 Olympus Optical Co Lösungsmittel zum reinigen und trocknen
US5403402A (en) * 1994-01-07 1995-04-04 Dow Corning Corporation Method of removing coating from surfaces
US7534304B2 (en) * 1997-04-29 2009-05-19 Whirlpool Corporation Non-aqueous washing machine and methods
US6059845A (en) * 1997-08-22 2000-05-09 Greenearth Cleaning, Llc Dry cleaning apparatus and method capable of utilizing a siloxane composition as a solvent
US6310029B1 (en) * 1999-04-09 2001-10-30 General Electric Company Cleaning processes and compositions
WO2001044256A1 (en) * 1999-12-17 2001-06-21 General Electric Company Process for stabilization of siloxanes by contacting them with water
US6691536B2 (en) 2000-06-05 2004-02-17 The Procter & Gamble Company Washing apparatus
US6706076B2 (en) 2000-06-05 2004-03-16 Procter & Gamble Company Process for separating lipophilic fluid containing emulsions with electric coalescence
US7018423B2 (en) 2000-06-05 2006-03-28 Procter & Gamble Company Method for the use of aqueous vapor and lipophilic fluid during fabric cleaning
US6930079B2 (en) 2000-06-05 2005-08-16 Procter & Gamble Company Process for treating a lipophilic fluid
US6939837B2 (en) 2000-06-05 2005-09-06 Procter & Gamble Company Non-immersive method for treating or cleaning fabrics using a siloxane lipophilic fluid
US6673764B2 (en) 2000-06-05 2004-01-06 The Procter & Gamble Company Visual properties for a wash process using a lipophilic fluid based composition containing a colorant
US6670317B2 (en) 2000-06-05 2003-12-30 Procter & Gamble Company Fabric care compositions and systems for delivering clean, fresh scent in a lipophilic fluid treatment process
US6840963B2 (en) 2000-06-05 2005-01-11 Procter & Gamble Home laundry method
CA2410199C (en) * 2000-06-05 2007-01-02 The Procter & Gamble Company Bleaching in conjunction with a lipophilic fluid cleaning regimen
AU2005200835B2 (en) * 2000-06-05 2006-03-30 The Procter & Gamble Company Domestic fabric article refreshment in integrated cleaning and treatment processes
US6840069B2 (en) 2000-06-05 2005-01-11 Procter & Gamble Company Systems for controlling a drying cycle in a drying apparatus
US6706677B2 (en) 2000-06-05 2004-03-16 Procter & Gamble Company Bleaching in conjunction with a lipophilic fluid cleaning regimen
US6855173B2 (en) 2000-06-05 2005-02-15 Procter & Gamble Company Use of absorbent materials to separate water from lipophilic fluid
US6828292B2 (en) * 2000-06-05 2004-12-07 Procter & Gamble Company Domestic fabric article refreshment in integrated cleaning and treatment processes
US6564591B2 (en) 2000-07-21 2003-05-20 Procter & Gamble Company Methods and apparatus for particulate removal from fabrics
CN1246440C (zh) 2001-05-30 2006-03-22 日本油脂株式会社 干洗用洗涤剂组合物
DE60207255T2 (de) * 2001-07-10 2006-08-10 The Procter & Gamble Company, Cincinnati Zusammensetzungen und verfahren zum entfernen von verschmutzungen von stoffartikeln
CA2455958A1 (en) 2001-09-10 2003-03-20 The Procter & Gamble Company Down the drain cleaning system
US6972279B2 (en) 2001-09-10 2005-12-06 Procter & Gamble Company Silicone polymers for lipophilic fluid systems
JP2004331849A (ja) * 2003-05-08 2004-11-25 Mihama Kk 洗浄剤組成物及び物品の洗浄方法
US7318843B2 (en) 2003-06-27 2008-01-15 The Procter & Gamble Company Fabric care composition and method for using same
US7202202B2 (en) 2003-06-27 2007-04-10 The Procter & Gamble Company Consumable detergent composition for use in a lipophilic fluid
US7365043B2 (en) 2003-06-27 2008-04-29 The Procter & Gamble Co. Lipophilic fluid cleaning compositions capable of delivering scent
US7345016B2 (en) 2003-06-27 2008-03-18 The Procter & Gamble Company Photo bleach lipophilic fluid cleaning compositions
US8148315B2 (en) 2003-06-27 2012-04-03 The Procter & Gamble Company Method for uniform deposition of fabric care actives in a non-aqueous fabric treatment system

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4324595A (en) * 1979-08-31 1982-04-13 Dow Corning Corporation Method for removing tacky adhesives and articles adhered therewith
GB2074184B (en) * 1980-04-19 1983-06-02 Dow Corning Ltd Compositions for treating hair and other fibrous materials
DE3114969C2 (de) * 1980-04-19 1986-04-03 Dow Corning Ltd., London Flüssige Waschmittelzusammensetzung

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8262741B2 (en) 1997-04-29 2012-09-11 Whirlpool Corporation Non-aqueous washing apparatus and method
US7695524B2 (en) 2003-10-31 2010-04-13 Whirlpool Corporation Non-aqueous washing machine and methods
US7739891B2 (en) 2003-10-31 2010-06-22 Whirlpool Corporation Fabric laundering apparatus adapted for using a select rinse fluid
US7837741B2 (en) 2004-04-29 2010-11-23 Whirlpool Corporation Dry cleaning method
US7966684B2 (en) 2005-05-23 2011-06-28 Whirlpool Corporation Methods and apparatus to accelerate the drying of aqueous working fluids

Also Published As

Publication number Publication date
CA1239326A (en) 1988-07-19
JPS61119765A (ja) 1986-06-06
JPS6350463B2 (de) 1988-10-07
EP0182583A2 (de) 1986-05-28
AU585906B2 (en) 1989-06-29
EP0182583A3 (en) 1988-04-06
AU4981785A (en) 1986-05-22
DE3583377D1 (de) 1991-08-08

Similar Documents

Publication Publication Date Title
EP0182583B1 (de) Verfahren zum Reinigen von Textilien mit cyclischen Siloxanen
US4685930A (en) Method for cleaning textiles with cyclic siloxanes
US3748268A (en) Spot and stain removing composition
EP0994977B1 (de) Feuchtwischtuch und verfahren zu seiner verwendung
JP3001980B2 (ja) シャワー設備すすぎ洗浄用水性組成物及びシャワー設備を清浄に保持する方法
US4909962A (en) Laundry pre-spotter comp. providing improved oily soil removal
JPH10501841A (ja) 過酸化水素を含む軟質面洗浄組成物
JPH057015B2 (de)
JP2000313900A (ja) クリーニング組成物並びに方法
JP2000319694A (ja) ドライクリーニング組成物並びに方法
JP2002506924A (ja) 液体多相洗剤
GB2194547A (en) Laundry pre-spotter composition providing oily soil removal
JPH10501845A (ja) 絨毯洗浄および回復組成物
KR20040052506A (ko) 건식 세정용 세정제 조성물
JP4294472B2 (ja) 布帛物品から偶発的な汚れを除去するための組成物及び方法
JPH0631404B2 (ja) ガラスセラミツク表面用清浄および／または状態調節剤
JP4312795B2 (ja) 親油性流体系で使用するための布地物品処理組成物
WO2001079415A1 (en) Fabric treatment article and composition
JP3556806B2 (ja) 洗浄剤組成物
JPH04216831A (ja) 硬質表面の保護方法
JP2003105394A (ja) ジェルクリーナー
US2327495A (en) Process of removing wax from
CA2460760A1 (en) Non-toxic cleaning composition
JP3636613B2 (ja) ドライクリーニング洗浄方法及びこの方法に用いる洗浄剤組成物
JP3611703B2 (ja) ドライクリーニング用洗浄剤組成物

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB

17P Request for examination filed

Effective date: 19880907

17Q First examination report despatched

Effective date: 19890704

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB

REF Corresponds to:

Ref document number: 3583377

Country of ref document: DE

Date of ref document: 19910808

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19970904

Year of fee payment: 13

Ref country code: DE

Payment date: 19970904

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19970909

Year of fee payment: 13

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19981112

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19981112

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990730

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990901