Patent Application
20060100120
(1) Field of the Invention
The present invention relates generally to a cleaning wipe and, more particularly, to a cleaning wipe with an all-purpose cleaning composition for use in cleaning textiles, glass, automobiles, and hard surfaces.
(2) Description of the Prior Art
There are a large number of cleaning products currently on the market. Typically, cleaning compositions, detergents, and the like contain a combination of many components including but not limited to anionic surfactants, cationic surfactants, nonionic surfactants, builders, suds-stabilizers, buffers, disinfecting agents, wetting agents, and chelating agents. Often these cleaning compositions employ components that may have adverse effects on the environment such as phosphorous compounds, peroxygen compounds, chlorine bleach compounds, and fluorinated compounds.
Prior art related to this invention is as follows:
U.S. Pat. No. 6,720,297 issued to Jenevein on Apr. 13, 2004 for a cleaning composition teaches a cleaning composition for treating and removing stains from a non-porous surface has one or more salts, such as quaternary ammonium salts, sulfates and chlorides, a chelator and a dispersant, dissolved in an aqueous solution of alcohol. The preferred salts are myristyltrimethylammonium bromide and benzethonium chloride, the chelator is tetrasodium salt ethylenediamine of tetraacetic acid, and the dispersant is polyvinyl alcohol. The cleaning composition is incorporated into a product, which has a non-woven polyester carrier impregnated with the cleaning composition.
U.S. Pat. No. 5,759,980 issued to Russo, et al. on Jun. 2, 1998 for a car wash teaches a novel car wash composition substantially eliminates water-spotting. This novel car wash composition is comprised of: a surfactant package which is comprised of a first surfactant selected from the group consisting essentially of an anionic surfactant, a nonionic surfactant and mixtures thereof; and a second surfactant selected from the group consisting essentially of fluorosurfactant, a silicone surfactant, and mixtures thereof; and a substantive polymer that renders the surface to be cleaned more hydrophilic.
U.S. Pat. No. 6,732,747 issued to Wise on May 11, 2004 for a composition and method for cleaning and disinfecting a garbage disposal teaches an improved composition and method for cleaning and disinfecting a garbage disposal that does not require aerosol propellants or carbon dioxide gas generating reaction systems. The composition comprises a suds stabilizing surfactant and a disinfecting agent, plus other optional ingredients such as additional detergent surfactant and scouring agents. The required disinfecting agent is selected from the group consisting of quaternary ammonium compounds, halogenated compounds, phenolics, alcohols, aldehydes, oxidizing agents and mixtures thereof.
U.S. patent application Pub. No. 20040043041 to Baker, et al. on Mar. 4, 2004 for antimicrobial compositions and methods of use teaches compositions and methods for decreasing the infectivity, morbidity, and rate of mortality associated with a variety of pathogenic organisms and viruses. The reference invention also relates to methods and compositions for decontaminating areas colonized or otherwise infected by pathogenic organisms and viruses. Moreover, the reference invention relates to methods and compositions for decreasing the infectivity of pathogenic organisms in foodstuffs. In particular, decreased pathogenic organism infectivity, morbidity, and mortality are accomplished by contacting the pathogenic organism with an oil-in-water nanoemulsion comprising an oil, an organic solvent, and a surfactant dispersed in an aqueous phase. In some preferred embodiments, the solvent comprises an organic phosphate solvent. In still other embodiments, the organic phosphate-based solvent comprises dialkyl phosphates or trialkyl phosphates (e.g., tributyl phosphate).
While these compositions can lead to a useful cleaning agent, a simpler composition that retains superior cleaning activity while reducing the number of components could simplify the manufacturing process potentially reducing production costs without sacrificing product quality. Further, many of these cleaning compositions employ components that may have adverse effects on the environment. Thus, there remains a need for a superior cleaning composition having a simple composition that is environmentally friendly, easily formulated, and cost effective.
The present invention is directed to a cleaning wipe for use in cleaning a range of materials including but not limited to textiles, glass, automobiles, and hard surfaces. Thus, the present invention provides a cleaning wipe comprising a wipe material and a cleaning composition; the cleaning composition comprising a water-soluble organic solvent, at least one surfactant which comprises at least one amide, a chelating agent a photoreactive agent, and distilled water; thereby providing a superior cleaning wipe having a simple composition that is easily formulated, and cost effective.
The present invention provides an all-purpose cleaning wipe with superior cleaning ability for a range of materials including but not limited to textiles, glass, automobiles, and hard surfaces.
The cleaning wipe includes a wipe material and a cleaning composition. The cleaning wipe may further include at least one preservative. The cleaning wipe may further include at least one enhancing agent.
Wipe Material
The wipe material can be from any of a variety of materials that can absorb the cleaner. For example, the wipe material preferably includes or is made of biodegradable materials, especially cellulose-based products, such as paper, cotton, hemp, kenaf, and the like. Other wood-based paper substitutes can also be used as the wipe material. For examples of known wipe materials see U.S. Pat. Nos. 6,821,940, 6,489,284, 5,141,803, and 4,753,844 and U.S. patent application Pub. Nos. 20040029763, 20020174500, and 20020155772, which are incorporated herein by reference in their entirety.
Wipe Material Fabrication
The wipe material can be fabricated by a variety of methods to provide a lightweight stable carrier or substrate for the cleaning composition, including, woven, non-woven, knitted, stitch bonded, and the like. Preferably, the wipe material is fabricated as a nonwoven, which provides a low cost, lightweight material of reasonable strength.
Preferably, the wipe material absorbs and holds highly-evaporative cleaners, such as products that evaporate by photoreaction or by low vapor pressure. A photo-reactive agent provides for oxidation of organic residues, thereby providing rapid evaporation of organic residue.
A useful wipe may bind the cleaning solution to prevent rapid evaporation, but release the solution when activated. For example, such activation may occur by compression or wringing.
The wipe material may include or be made of different materials and material arrangements to enhance performance. For example, the wipe material can be a multi-ply material. In an example multi-ply embodiment, different materials are used in the plies in order to extend the useable life of each wipe. For example, one side of the wipe can be covered by a non-wicking and/or non-translucent material ply such that when the wipe is laid on a surface with this surface upward, the evaporation of the cleaning solution is retarded.
In another embodiment, a ply in a multi-ply embodiment is a water-insoluble material that forms a partially hydrophobic nonwoven layer that preferentially absorbs hydrophobic solutions, thereby making the wipe more efficacious for cleaning of oils and grease.
Cleaning Composition
The cleaning composition contains the following components:
(a) at least one water-soluble organic solvent present in a solubilizing effective amount;
(b) a first surfactant which comprises at least one amide which may be the product of the saponification of at least one fatty acid by an amino alcohol in a water-soluble organic solvent, wherein the first surfactant is present in a cleaning-effective amount;
(c) at least one additional surfactant present in a cleaning-effective amount;
(d) a chelating agent capable of chelating multivalent metal ions, wherein the chelating agent is present in an amount effective to prevent phase reversal of the oil-in-water emulsifier; and
(e) the remainder, distilled water.
Additional adjuncts in small amounts such as fragrance, dye and the like can be included to provide desirable attributes of such adjuncts.
In the application, effective amounts are generally those amounts listed as levels of ingredients in the descriptions which follow hereto. Unless otherwise stated, amounts listed in percentages are in weight percents (%'s) of the composition.
Solvent
The solvent should be a water-soluble organic solvent. Further, the solvent is preferably a water-soluble organic alcohol. The most preferred water-soluble organic solvent is tetrahydrofurfuryl alcohol (THF-A). THF-A is an organic solvent that is completely miscible with water. THF-A has an extensive history of use as a highly versatile, high purity solvent. Due to its relatively benign nature and the fact that it is not oil-based, THF-A is generally regarded as a “green” solvent in industrial applications. THF-A readily biodegrades in soil, sludge, and water. The atmospheric half life is 13 hours. Unused THF-A is not classified as a hazardous waste under the Resource Conservation and Recovery Act.
Surfactants
The first surfactant is at least one amide. The preferred amide is at least one naturally occurring amide. The most preferred amide is a member of the group of amides comprising compounds with the structure CH3(CH2)xCONH(CH2)2OH, wherein the value of x is preferably any whole number between and including 14 and 22; CH3(CH2)xCH═CH(CH2)yCONH(CH2)2OH, wherein the value of x+y is preferably any whole number between and including 12 and 16; CH3(CH2)xCH═CH(CH2)yCH═CH(CH2)zCONH(CH2)2OH, wherein the value of x+y is preferably any whole number between and including 10 and 14; and mixtures thereof.
In another embodiment, the first surfactant may be the product of the saponification of at least one fatty acid by an amino alcohol in a water-soluble organic solvent. The preferred at least one fatty acid is chosen from the group comprising saturated fatty acids of the general formula CxH2xO2, wherein the value of x is preferably any whole number between and including 16 and 24; monounsaturated or polyunsaturated fatty acids of the general formula CxH(2x−y)O2, wherein the value of x is preferably any whole number between and including 16 and 20 and the value of y is preferably either 2 or 4; and mixtures thereof. A more preferred fatty acid is one chosen from the group comprising palmitic acid; palmitoleic acid; stearic acid; oleic acid; linoleic acid; 5,9,12-octadecatrienoic acid; 5,11,14-eicosatrienoic acid; cis,cis-5,9-octadecadienoic acid; cis-11-octadecanoic; eicosanoic acid; docosanoic acid; tetracosanoic acid; and mixtures thereof. The most preferred fatty acid is tall oil also known as pine oil. Tall oil is commercially available as MeadWestvaco L-5, marketed by MeadWestvaco, which comprises at least 95% tall oil fatty acid and less than 5% rosin acids. Any suitable fatty acid may contain rosin acids present in small amounts not to exceed about 5% by weight of the total weight of the fatty acid. The preferred amino alcohol is an ethanolamine. The most preferred amino alcohol is monoethanolamine.
The at least one additional surfactant is a polyethylene oxide condensate of an alkyl phenol. Suitable additional surfactants are octylphenol ethoxylates that have the chemical formula C8H17(C6H4)O(CH2CH2O)xH, wherein the average value of x for any mixture of these compounds is preferably any number between and including 3 and 11. Optimally two additional surfactant mixtures are used, wherein the average value of x for the first additional surfactant mixture is preferably 4.5, and wherein the average value of x for the second additional surfactant mixture is preferably 9.5. These preferred additional surfactant mixtures are commercially marketed under the names Triton X-45 and Triton X-100 by The Dow Chemical Company.
Chelating Agent
The chelating agent is required to chelate multivalent metal ions and thus prevent phase reversal of the oil-in-water emulsifier. The preferred chelating agent is an aminocarboxylic acid salt. The most preferred chelating agent is tetrasodium ethylenediaminetetraacetic acid (Na4EDTA). This compound is commercially marketed as an aqueous solution of about 38% by weight Na4EDTA under the name Versene by The Dow Chemical Company.
Water and Miscellaneous
Water may be present at levels of about 99.6% by volume. Some of the amides and acids that are present in this composition are known to undergo intermolecular and intramolecular Diels-Alder cyclization reactions. Some of the products of those reactions are known to have biological activity. Because these products are present in the cleaning composition of the current invention, and these products show biological activity, no additional biocide is necessary in this composition at the higher concentrations. At the lower concentrations, a biocide or other type of preservation may be utilized to prevent deterioration. By way of example, but not limitation one of these cyclization products is cyclopinolenic acid. Additionally, small amounts of adjuncts may be added to the composition for aesthetic qualities. These adjuncts include perfumes and dyes.
Preservatives
Wipes are stored for substantial periods of time prior to use and therefore need to be protected against microbial contamination and deterioration to which they are readily susceptible, especially if biodegradable. One common method to achieve this is to incorporate a suitable chemical preservative system in the liquid composition employed to impregnate the nonwoven wipe. The present invention provides for the inclusion of any biodegradable preservative system.
Various preservative systems have been employed in a number of aqueous impregnating compositions for wipes. These include ethyl alcohol, including as part of a preservative system that comprises sorbic acid, citric acid and ethyl alcohol. Other preservatives include cationic antimicrobial agents [U.S. Pat. Nos. 3,264,188, 4,615,937 and 4,678,704], such as quaternary ammonium compounds and organo-silicon quaternary ammonium salt, bisguanides and polymeric bisguanide such as polyhexamethylene bisguanide hydrochloride, benzalkonium chloride, and polyhexamethylene biguanide hydrochlorides as antimicrobial agents in combination with certain amine oxides in aqueous antimicrobial compositions [U.S. Pat. No. 4,587,266].
Alternatively, the wipes can be sterilized for storage via non-chemical means. For example, the wipes can be sterilized by heat, radiation, filtration, or combinations of these methods.
Heat sterilization can include ultra high temperature (UHT) sterilization, which involves subjecting the solution and/or wipes to temperatures in excess of 100 degrees Fahrenheit for an adequate period of time and then packaging in air-tight containers. This high temperature is necessary to inactivate any thermoresistant spores that may be in the wipe components. In an example of the process, the cleaning solution can be sterilized at 135 degrees Fahrenheit for 2-5 seconds to achieve sterilization. In one preferred embodiment, for example for ultra-sterilization applications like hospitals, the solution is sterilized below its flashpoint in order to prevent ignition if accidentally exposed to an oxidant. Even more preferably, the solution is sterilized during manufacturing.
Alternatively, the cleaning solution can be sterilized by filtration. Filtration methods can include microporous filtration or ultrafiltration.
The wipes may also be sterilized by radiation, such as ultraviolet irradiation, gamma irradiation or particle beam irradiation. The wipes may also be sterilized by a combination of these techniques. For example, the wipe material and wipe containers can be sterilized by uv or gamma-irradiation and the solution sterilized by the UHT process, then the solution added to the wipe material in a sterile atmosphere.
Enhancing Agents
The wipe cleaning composition or wipe material may include at least one enhancing agent. By way of example, and not limitation, the at least one enhancing agent can be a skin softening and conditioning agent, a pH control agent, a malodor reducing system, an alcohol, a soil resist, an aromatherapy agent, and combinations thereof.
The invention further provides a method for formulating the cleaning concentrate.
The method of formulating the cleaning composition of the present invention relies upon adherence to certain process parameters that lead to a unique product. The order of addition of the various components is critical. It is also vital that the process temperature be maintained throughout the procedure.
The composition is formulated in a reactor. The preferred reactor is a glass or Hastelloy reactor equipped with a reflux condenser and a means of stirring. The means of stirring may be a stir bar or agitator. The reactor should be clean prior to the reaction.
The reactor is charged with a water-soluble organic solvent. A suitable amount of water-soluble organic solvent is between about 3% and about 16% by weight of the total composition. The most preferred amount of water-soluble organic solvent is between about 3% and about 9% by weight of the total composition. In a preferred embodiment the water-soluble organic solvent is a water-soluble organic alcohol. In the most preferred embodiment the water-soluble organic solvent is tetrahydrofurfuryl alcohol (THF-A).
The reactor is charged with an amino alcohol. The stirring mechanism is employed while the reactor is charged with the amino alcohol. The stirring mechanism is continuously employed during the remainder of the process. A suitable amount of amino alcohol is between about 3% and about 9% by weight of the total composition. The amino alcohol undergoes a chemical reaction with the fatty acid in a 1 to 1 mole ratio. However, in the preferred embodiment the fatty acid is present in excess amounts. In a preferred embodiment the amino alcohol is an ethanolamine. In the most preferred embodiment the amino alcohol is monoethanolamine.
The contents of the reactor must be heated. The preferred temperature range for this process is between 75 and 90 degrees Celsius (C). The most preferred temperature range for this process is between 80 And 85 degrees C. This temperature range is maintained throughout the process. Immediately following additions of various components the batch temperature may fall below this range. At no time should the temperature be allowed to fall below 55 degrees C. The batch temperature should recover quickly to the required range.
At least one fatty acid is added to the reactor. A suitable amount of the at least one fatty acid is between about 7% and about 14% by weight of the total composition. The fatty acid is added via a clean gravity feed vessel. Alternatively a pump type vessel may be employed for the addition. After addition of the fatty acid the contents of the reactor are stirred for a first time period during which the reaction is monitored until it is complete. The reaction may be determined to be complete by any convenient method used in the art.
Suitable methods include thin layer chromatography and high performance liquid chromatography.
After the reaction is determined to be complete, a first portion of distilled water is added rapidly. A suitable amount of the first portion of distilled water is between about 1% and about 9% by weight of the total composition. The mixture is stirred for a second time period which is sufficient to allow the composition to form a homogeneous mixture. Preferably the mixture is stirred for at least 10 minutes. The stirring time may increase dramatically corresponding with a scale-up of the process.
The at least one additional surfactant is rapidly added to the reactor. A suitable amount of each additional surfactant is between about 7% and about 30% by weight of the total composition. The most preferred amount of each additional surfactant is between about 8% and about 30% by weight of the total composition. The mixture is stirred for a time period which is sufficient to allow the composition to form a homogeneous mixture. Preferably the mixture is stirred for at least 10 minutes. The stirring time may increase dramatically corresponding with a scale-up of the process.
The chelating agent is added to the reactor. The preferred amount of chelating agent is between about 2% and about 8% by weight of the total composition. The chelating agent may be added to the present composition as an aqueous solution. In a preferred embodiment the chelating agent is added to the composition as an aqueous solution, and the chelating agent is present at a concentration of between about 36% and about 40% by weight in the aqueous solution. A commercially available aqueous solution of a chelating agent, such as Versene, may be used. A suitable amount of the aqueous solution of chelating agent is between about 7% and about 19% by weight of the total composition. The most preferred amount of the aqueous solution of chelating agent is between about 8% and about 19% by weight of the total composition.
Distilled water is added to the reactor. The distilled water makes up the balance of the composition. A preferred amount of distilled water for the second addition of distilled water is between about 4% and about 44% by weight of the total composition. The composition is allowed to cool to within 25 to 30 degrees C.
Optionally, after cooling and prior to commercial distribution, the composition may be passed through a filter to remove any debris acquired during the processing steps.
Certain modifications and improvements will occur to those skilled in the art upon a reading of the foregoing description. By way of example, applications for this cleaning composition may be extended to a cleaner for aircrafts which have exterior coatings similar or identical to automobiles. All modifications and improvements have been deleted herein for the sake of conciseness and readability but are properly within the scope of the following claims.
Design Example(s)
This section outlines a design example, not necessarily optimized but illustrative of a suitable method, wherein the cleaning composition of the current invention may be formulated.
In this preferred embodiment of the method of formulating a cleaning composition in a concentrated form a reactor is charged with tetrahydrofurfuryl alcohol. The reactor is then charged with monoethanolamine, wherein the volume of monoethanolamine is one half the volume of the tetrahydrofurfuryl alcohol. The contents of the reactor are heated to within the range of 80 to 90 degrees C. The reactor is charged with tall oil (MeadWestvaco L-5) acquired from MeadWestvaco. The volume of tall oil is equal to the volume of the tetrahydrofurfuryl alcohol. The contents of the reaction are stirred until the reaction is determined to be complete. The reaction progress is followed by thin layer chromatography. The reactor is charged with a first portion of distilled water, wherein the volume of the first portion of distilled water is equal to the volume of the tetrahydrofurfuryl alcohol. The contents of the reaction are stirred for ten minutes. The reactor is charged with the additional surfactants Triton X-100 and Triton X-45, acquired from the Dow Chemical Company, wherein the amount of each additional surfactant is equal to the volume of the tetrahydrofurfuryl alcohol. The contents of the reactor are stirred for ten minutes. The reactor is charged with the commercially available aqueous solution of tetrasodium ethylenediaminetetraacetic acid Versene, wherein the amount of Versene is equal to the volume of the tetrahydrofurfuryl alcohol. The reactor is charged with a second portion of distilled water, wherein the volume of the second portion of distilled water is equal to five times the volume of the tetrahydrofurfuryl alcohol, and the mixture is allowed to cool to about room temperature.
This nonprovisional utility patent application is copending with nonprovisional application No. 10/868,649 filed on Jun. 15, 2004, and nonprovisional application No. 10/868,541 filed on Jun. 15, 2004, and nonprovisional application No. 10/868,464 filed on Jun. 15, 2004.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10868464 | Jun 2004 | US |
| Child | 11301044 | Dec 2005 | US |
