Patent Application
20160024320
1. Field of the Invention
This invention relates to paint and varnish remover compositions, and more particularly, to a method of activating the solvents free from NMP for more effective paint and varnish removing action, and to compositions thereof.
Additional attributes of the inventive compositions are: non flammable, biodegradable, environmentally benign for industrial and consumer use, easy washability, and compatible with existing commercial paint stripping compositions and/or components.
2. Description of the Prior Art
The term ‘varnish and paint remover’ as applied herein refers to chemical compositions which can strip or facilitate stripping of coatings, such as, paint, varnish, lacquer, shellac, polyurethane finishes and enamels, used to protect substrates such as wood and metal and to beautify them. Methylene chloride paint strippers are currently the industry standard for stripper performance. Methylene chloride strippers are effective for quickly softening most types of paints. The speed at which methylene chloride performs is believed to be due to its high solvent power coupled with high volatility as reflected by its extremely fast evaporation rate. This high volatility shortens the work life of methylene chloride paint strippers. Frequently, when methylene chloride paint strippers are used on thick accumulations of paint, more than one application is required since the work life is insufficient to permit penetration through the accumulation of paint.
Methylene chloride is a chlorinated solvent which is closely regulated for environmental protection. Recently, it was discovered that methylene chloride can cause tumors in rats and mice. Since that discovery, the wide use of that solvent by industry and consumers has come under close scrutiny by federal regulatory agencies.
N-methyl-2-pyrrolidone (NMP) has been employed in place of methylene chloride as the active ingredient in paint stripper compositions. Nelson, in U.S. Pat. No. 4,759,510, for example. described a composition for this use having low volatility which included about 20% to 90% by weight of NMP and 30% to 70% by weight of an aromatic hydrocarbon solvent. Mixtures of NMP and .gamma.-butyrolactone (BLO) also have been used as liquid formulations for removing screen printing inks. Madsen, in U.S. Pat. No. 4,836,950, incorporated herein by reference, for example, described such a liquid composition which included 1-25% by volume of NMP and/or BLO. Valasek, similarly, in U.S. Pat. No. 4,664,721, incorporated herein by reference, described a composition which included 30-85% by weight of NMP and 10-35% by weight of an oxygenated solvent selected from esters and ethers. BLO was mentioned as a suitable ether, although butoxyethanol and cyclohexanone were preferred. Caster, in U.S. Pat. No. 4,865,7587 incorporated herein by reference, described a method of removing paint with a lower alkyl substituted 2-oxazolidinone. In comparative results reported therein, it was disclosed that ethyl 3-ethoxypropionate had no effect on paint removal. McCullins, in British Patent 1,487,737, described a paint remover composition for aerosol type paints in the form of a gel which included methyl ethyl ketone, ethyl acetae, ethoxyethanol and 2-ethoxyethyl acetate. This mixture of solvents was considered effective for paint sprayed graffiti as a viscous, transparent gel containing particles of silica or alumina in suspension. Palmer, in U.S. Pat. No. 4,120,810, incorporated herein by reference, described paint remover compositions of NMP and/or BLO, and at least 35 mole % of blends of alkyl naphthalenes and alkyl benzenes. These and other compositions, however, have not proven particularly effective for removing paint and varnish from wood and metal surfaces, without containing objectionable halogenated or aromatic compounds. Furthermore, they do not possess the attributes of being biodegradable non-flammable, having a low vapor pressure and low toxicity. Narayanan et al in U.S. Pat. No 5,098,592 incorporated herein by reference, have shown that a synergistic combination of NMP, BLO and ethyl 3-ethoxypropionate (EEP) is a very effective compositions for removing varnish and several type of paints from wood and metal substrates. Recently use of NMP for consumer applications is not environmentally favorable because of reproductive toxicity profile of NMP.
Accordingly, it is the object of the present invention to satisfy the above criteria for an environmentally safe commercial product free from NMP for removing paint and varnish from surfaces, and to perform such removal effectively with less material than other related products on the market today.
These and other objects and features of the invention will be made apparent from the following description of the invention. The replacement of NMP with an environmentally benign solvent or mixtures of solvents has the following criteria.
I have discovered a new composition for removing or stripping varnish and paint from surfaces such as wood or metal which avoids the inclusion of N-methyl-2-pyrrolidone and other environmentally undesirable components.
More particularly, the composition of the present invention comprises an activating amide ester, BLO and Ethyl 3-ethoxy propionate (EEP). Preferably, about 1-20% by weight of EEP, preferably 2-15% by weight and optimally about 3-5% by weight is present. In addition, a method is provided herein which is particularly effective for removing or tripping varnish and paint from surfaces such as wood or metal which comprises applying the inventive composition containing an activated amide ester, and BLO with 1-20% by weight of ethyl 3-ethoxypropionate (EEP), preferably 2-15%, and optimally about 3-5% to the surface to be stripped and thereafter removing the composition along with the stripped material. Other components may be included in the composition, for example, Pentanoic acid, 5-(dimethylamino)-4-methyl-5-oxo-methyl ester (Rhodiasolv R Polarclean), Pentanoic acid, 2-methyl, dimethyl ester (Rhodiasolv IRIS). Bis N N-dimethyl methyl glutaramide may also be present in commercial sample and Commercially available co-solvent [amide ester] may be a mixture of the three solvents listed above: Amide ester (>95%) and the balance made up with diamide and diester (herein referred to as CEA) as shown hereinafter,
In a suitable embodiment of the invention, the activated composition herein includes about 20-70% of the activated amide, 30-80% BLO and 1-30% EEP, preferably 30-65% of the activated amide, 35-70% BLO and 2-15% EEP, and optimally, 35-39% of the activated amide, 55-59% BLO and 3-5% EEP.
The method of the invention provides activation for CEA and BLO and a synergistic effect for paint and varnish removal with less material than used previously with other related compositions, and in a safe and environmentally acceptable manner.
Typical paint and varnish remover compositions of the present invention include the following components.
Other Co-solvent combinations as defined above would work along with an activator (see below for definition). Other activators can be used with different % wt. (Methylene chloride for example can be used at 10 -50%) Acids/Bases/silicones can also be used as additional activators.
0-0.5
0-0.2
As described in Table 1, the essential components of the paint and varnish remover composition of the invention include synergistic mixed solvents: BLO/PC/DMI and CEA/PC/DMI which are activated by ethyl 3-ethoxypropionate (EEP). The activator compound EEP is available from Eastman Chemicals as Ektapro® EEP solvent. The presence of EEP in the composition activates the solvents so that more effective paint and varnish removal action is achieved. Since EEP reduces the flash point of the composition, which is not desirable, it is preferred to use the lower end of the suitable range of the activating effect of EEP. The composition of the present invention may contain optionally, one or more of the group of a surfactant, a thickener, a fragrance, a bittering agent and a diluent.
Suitable surfactants include non-ionic surfactants with HLB ranging from about 8-18, selected from:
Examples of surface active agents which may be used are those supplied under the following trade names with approximate e Chemical Constitution:
Thickeners may also be included in the inventive composition. The preferred thickeners or gelling agents are cellulose derivatives which have the property of both water and organic solvent solubility. Cellulose derivatives of this type which are of particular interest are those ether derivatives containing etherifying groups selected from hydroxyalkyl groups and groups derived therefrom, such etherifying groups containing preferably up to about 5 or 6 carbon atoms. The gelling agent may also comprise cellulose ether derivatives which, in addition to etherifying groups selected from hydroxyalkyl groups and groups derived therefrom, contain other types of etherifying groups, especially small alkyl groups of, for example, one or two carbon atoms. However, such etherifying groups generally confer properties upon the cellulose derivative which are less acceptable for the present purpose, and the gelling agent is therefore conveniently substantially restricted to cellulose ether derivatives containing etherifying groups selected from hydroxyalkyl groups and groups derived therefrom.
Etherifying groups consisting of or derived from hydroxyalkyl groups containing up to 5 carbon atoms, particularly 2, 3 or 4 carbon atoms, are preferrede. The hydroxypropyl celluloses, for example, have been found to be of particular value in giving a substantially transparent gel system with a suitable solvent system and in imparting quite adequate thickening and film-forming properties in their own right without the need of any other agents for these purposes. Conveniently, the hydroxypropyl group in such celluloses is derived from isopropanol rather than n-propanol but a number of variations in structure are possible even when this is the case. Thus, not all of the free hydroxy groups of the cellulose need necessarily be substituted and, if desired, the hydroxy groups of certain hydroxypropyl groups may, in turn, be substituted by a further hydroxypropyl group (as for example, in the Klucel® materials described below). Hydroxypropyl celluloses employed in compositions according to the present invention conveniently have molecular weights in the range from about 50,000 to about 1,000,000, preferably from about 800,000 to 1,000,000.
One form of hydroxypropyl cellulose which has been used with advantage is marketed under the trade name Klucel H . Klucel® H has a similar chemical structure to Klucel® MS 3.0 which may also be used, but is of higher molecular weight, and possesses particular advantages in terms of the viscosity of its solutions. Thus, a 1% solution of Klucel® H in water has a viscosity in the range from 1,500 to 2,500 units and in ethanol the range is 1,000 to 2,500 units while solutions of Klucel® MS 3.0, particularly in ethanol, have a lower viscosity. The property of possessing a substantially similar viscosity in organic solvent and aqueous solutions is a valuable one for gelling agents used in compositions according to the present invention. The proportion of gelling agent required in the compositions in order to give good gels, depends in part on the molecular weight of the gelling agent used, the usual range being from 0.25% to 2%. Thus, for example, with the usual proportion of gelling agent of from about 0.25% or 0.5% upwards is suitable for high molecular weight materials and of from about 2% upwards is suitable for low molecular weight materials. For high molecular weight materials, for example of molecular weights of 800,000 to 1,000,000, a proportion of above 1.5% is preferably avoided as it leads to a gel of too great a viscosity. With low molecular weight materials, larger proportions may be used before such a position is reached and, if the molecular weight is low enough, amounts of up to 10% or even 20% or more may be used. It will be appreciated, however, that the use of a smaller amount of material of higher molecular weight is generally to be preferred.
A typical fragrance is oil of wintergreen (methyl salicylate) although many others known in the art may be included in the composition.
Suitable diluents include organic hydrocarbons such as dipentene and xylene, alkylene glycol ethers such as propylene glycol monomethyl ether, tripropylene glycol monomethyl ether, dipropylene glycol monomethyl ether and tetrahydrofurfuryl alcohol and propylene carbonate. Mixtures of these compounds also may be used.
A suitable bittering agent is denatoniurn benzoate although others known in the art may be used as well.
Representative compositions of the invention include the following Examples below:
1(polyoxyethylated (6) decyl alcohol)
Methodology used to determine relative efficacy of treatment compositions (extracted from U.S. Pat. No. 5,098,592):
In preliminary screening One drop of test formulation was applied to ½ inch times.; inch.times.24 panels of pine wood painted liberally with 3 coats of alkyd enamel paint and cured in air for 1 week and in an oven for 2 days at 50° C. The spots containing the reagents were scrapped of at 15 minutes and 30 minutes intervals and the relative paint stripping performance measured in terms of number of coats removed 3 being perfect, by visual evaluation. The efficacy test results were obtained upon 12 whole panels of wood inter-painted with 4 coats of air cured paint and varnish materials for 8-24 hours. The effectiveness is measured as the percentage of the 4 coats removed after 30 minutes of stripping time with brush application of sufficient test material to cover the surface completely. The panels were coated with the following materials.
While the compositions herein have been shown are formulated as solutions, it will be understood that other forms of the inventive compositions may be used as well, such as aerosol sprays, gels, lotions, creams, and the like.
| Number | Date | Country | |
|---|---|---|---|
| 62028408 | Jul 2014 | US |
