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Claims  |
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That which is claimed is:
1. A composition for removing a coating painted on a surface consisting
essentially of a solvent consisting essentially of 70-75% by weight
acetone; 5-10% by weight water; and 15-20% by weight volatile silicone
fluid having a vapor pressure less than 0.10 mm Hg: the volatile silicone
fluid being (i) a volatile short chain linear silicone fluid having only
methyl groups and alkyl groups with 6-12 carbon atoms as substituents on
silicon atoms, or (ii) a volatile short chain linear silicone fluid having
only methyl groups and phenyl groups as substituents on silicon atoms.
2. A composition according to claim 1 in which the volatile short chain
linear silicone fluid is 3-hexyl-1,1,1,3,5,5,5-heptamethyltrisiloxane,
3-octyl-1,1,1,3,5,5,5,-heptamethyltrisiloxane, or
3-phenyl-1,1,1,3,5,5,5-heptamethyltrisiloxane.
3. A composition according to claim 1 further comprising a volatile cyclic
silicone fluid having only methyl groups as substituents on silicon atoms,
mixed with the volatile short chain linear silicone fluid.
4. A composition according to claim 3 in which the volatile short chain
linear silicone fluid is 3-hexyl-1,1,1,3,5,5,5-heptamethyltrisiloxane,
3-octyl-1,1,1,3,5,5,5-heptamethyltrisiloxane, or
3-phenyl-1,1,1,3,5,5,5-heptamethyltrisiloxane, and the volatile cyclic
silicone fluid is decamethylcyclopentasiloxane.
5. A composition for removing a coating painted on a surface consisting
essentially of a solvent consisting essentially of 70-75% by weight
acetone; 5-10% by weight water; and 15-20% by weight volatile silicone
fluid having a vapor pressure less than 0.10 mm Hg: the volatile silicone
fluid being a compound having the formula:
##STR3##
in which n is 5-12.
6. A composition according to claim 5 in which the volatile silicone fluid
is 3-hexyl-1,1,1,3,5,5,5,-heptamethyltrisiloxane or
3-octyl-1,1,1,3,5,5,5-heptamethyltrisiloxane.
7. A composition according to claim 5 further comprising a volatile cyclic
silicone fluid having only methyl groups as substituents on silicon atoms,
mixed with the volatile silicone fluid.
8. A composition according to claim 7 in which the volatile silicone fluid
is 3hexyl-1,1,1,3,5,5,5-heptamethyltrisiloxane or
3-octyl-1,1,1,3,5,5,5-heptamethyltrisiloxane, and the volatile cyclic
silicone fluid is decamethylcyclopentasiloxane.
9. A composition for removing a coating painted on a surface consisting
essentially of a solvent consisting essentially of 70-75% by weight
acetone; 5-10% by weight water; and 15-20% by weight volatile silicone
fluid having a vapor pressure less than 0.10 mm Hg: the volatile silicone
fluid the compound:
##STR4##
10. A composition according to claim 9 further comprising a volatile cyclic
silicone fluid having only methyl groups as substituents on silicon atoms,
mixed with the volatile silicone fluid.
11. A composition according to claim 10 in which the volatile cyclic
silicone fluid is decamethylcyclopentasiloxane. |
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Claims  |
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Description  |
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BACKGROUND OF THE INVENTION
This invention is directed to the removal of paint such as enamels and
lacquers from organic and inorganic surfaces, including the removal of
nail polish from human or animal fingernails and toenails.
The problem to be solved according to this invention is the formulation of
VOC compliant compositions for use in the removal of paint.
American air pollution regulations limit the amount of organic solvents
that can be discharged into the atmosphere. The term used for solvents is
"volatile organic compounds" (VOC). A volatile organic compound (VOC) is
defined as any compound of carbon that has a vapor pressure greater than
0.10 millimeter of mercury at a temperature of twenty degrees Centigrade
and a pressure of 760 millimeters mercury.
"Volatile organic content" has been defined as the amount of volatile
organic compounds (VOC) liberated from a coating as determined by ASTM
D3690 and EPA Reference Method 24, which are standard industrial tests.
Under the definition, a volatile organic compound is any compound which
enters the atmosphere and photochemically reacts in the atmosphere with
nitrogen oxides to reduce ozone and form photochemical smog.
Reduction of VOC has been mandated in several American states, and
regulations in the state of California, for example, require less than
about 180 grams of volatiles per liter of product to enter the atmosphere.
This can be determined by baking ten grams of a product in an oven at one
hundred-ten degrees Centigrade for one hour. The amount of solids which
remain is subtracted from the total of the ten grams which was tested.
Calculations are based on the weight of the volatiles that have
evaporated, which is reported as grams per liter.
The United States federal Environmental Protection Agency (EPA) has
identified many volatile organic compounds present in consumer products
such as common solvents ethanol, isopropyl alcohol, kerosene, and
propylene glycol; and hydrocarbon solvents such as isobutane, butane, and
propane, which are often employed as propellants in industrial and
consumer products.
Some American states, including California under the auspices of the
California Air Regulation Board (CARB), have proposed standards which
would limit and reduce the amount of volatile organic compounds (VOC)
permitted in various consumer products, such as chemically formulated
products used by household and institutional consumers. These regulations
cover products such as detergents; cleaning compounds; polishes; floor
products; cosmetics; personal care products; home, lawn and garden
products; disinfectants; sanitizers: and automotive specialty products.
These CARB type standards would effect such widely used consumer products
as shaving lather, hairspray, shampoos, colognes, perfumes, aftershave,
deodorants, antiperspirants, suntan preparations, lotions, breath
fresheners, and room deodorants.
Thus, the problem of legal compliance and the need for new and novel
formulations and techniques for reducing organic emissions, should be more
than apparent.
SUMMARY OF THE INVENTION
The problem is solved in accordance with the present invention by
formulating paint removal compositions with one or more of certain
volatile cyclic or volatile linear silicones. These volatile silicones
have a vapor pressure below 0.10 mm Hg at twenty degrees Centigrade and
hence are not a VOC.
Thus, the object of the present invention is to provide a paint remover
which includes as an ingredient thereof, a volatile short chain linear or
cyclic silicone fluid having in its molecule methyl groups and either (i)
phenyl groups or (ii) alkyl groups containing up to twelve carbon atoms
but preferably six, seven, or eight carbon atoms.
The paint remover meets the various regulations mandated by American
Federal, State, and Local environmental regulations, on the use of
volatile organic compounds (VOC) in industrial products and consumer
oriented personal care products, and provides the solution to the problem
of being in full compliance with American air pollution regulations.
These and other features, objects, and advantages of the present invention
will become more apparent from a consideration of the following detailed
description thereof.
DETAILED DESCRIPTION OF THE INVENTION
A nail polish remover is used to remove traces of prior nail lacquer
coatings or residues from soap and hand creams, before a new nail lacquer
is applied to the fingernails or toenails. The main and major ingredient
of most nail polish removers is acetone. While quantities of acetone in
excess of about ninety percent by weight have been used in anhydrous nail
polish removers of the past, the maximum acetone content now mandated by
new and emerging environmental regulations is seventy-five (75) percent by
weight.
Nonsmear nail polish removers depend upon the presence of water in the
mixture. These aqueous mixtures contain at the most about ten (10) percent
by weight of water, since the presence of water increases the time
required for removing the nail lacquer from the nails.
Because of the environmental limitations on the use of acetone, some
suitable solvent replacement must now be included in both anhydrous and
aqueous nail polish removers.
According to this invention, the solvent replacement for acetone is an
organosilicon compound selected from the group consisting of (i) a
volatile short chain linear silicone fluid having in its molecule only
methyl groups, (ii) a volatile cyclic silicone fluid having in its
molecule only methyl groups, (iii) a volatile short chain linear silicone
fluid having in its molecule both methyl groups and phenyl groups, and
(iv) a volatile short chain linear silicone fluid having in its molecule
both methyl groups and alkyl groups containing up to twelve carbon atoms,
but preferably six, seven, or eight carbon atoms.
All of these fluids have a vapor pressure which is less than 0.10 mm Hg,
measured at twenty degrees Centigrade and 760 mm pressure, rendering them
acceptable under current non-VOC definitions.
One type of volatile silicone in accordance with the present invention is a
low viscosity methylsilicone fluid. The volatile low viscosity
methylsilicone fluid corresponds to the average unit formula
(CH.sub.3).sub.a SiO.sub.(4.a/2) wherein a is an integer having an average
value of from two to three. The methylsilicone fluid contains siloxane
units joined by Si--O--Si bonds. Representative units are (CH.sub.3).sub.3
SiO.sub.1/2, (CH.sub.3).sub.2 SiO.sub.2/2, (CH.sub.3)SiO.sub.3/2, and
SiO.sub.4/2. These units are present in molar amounts such that there is
provided an average of from about two to three methyl groups per silicon
atom in the methylsilicone fluid.
The volatile low viscosity methylsilicone fluid contains dimethylsiloxane
units and optionally trimethylsiloxane units. Preferably, the
methylsilicone fluid has a viscosity of less than about ten centistokes.
Representative compounds are cyclopolysiloxane compounds of the general
formula [(CH.sub.3).sub.2 SiO].sub.x, and linear siloxane compounds of the
general formula (CH.sub.3).sub.3 SiO[(CH.sub.3).sub.2 SiO].sub.y
Si(CH.sub.3).sub.3, in which x is an integer having a value of from three
to ten, and y is an integer having a value of from zero to about four.
The volatile low viscosity methylsilicones have boiling points generally
less than about two hundred-fifty degrees Centigrade, and possess
viscosities preferably generally less than about ten centistokes measured
at twenty-five degrees Centigrade. Most preferably, the viscosity is 0.65
to 5.0 centistokes. The cyclopolysiloxane compounds have been assigned the
adopted name "CYCLOMETHICONE" by The Cosmetics, Toiletries and Fragrance
Association, Inc., Washington, D.C. (CTFA). Both the cyclopolysiloxanes
and the linear siloxanes are clear fluids, and are essentially odorless,
nontoxic, nongreasy and nonstinging. Cosmetically, these methylsilicone
fluids are nonirritating to skin and nail surfaces, and exhibit enhanced
spreadability and ease of rub-out when applied. Once applied, the
materials evaporate leaving behind no residue.
Methylsilicone fluids which are operable in accordance with the present
invention leave substantially no residue after thirty minutes at room
temperature when one gram of fluid is placed at the center of a No. 1
circular filter paper having a diameter of 185 mm supported at its
perimeter in open room atmosphere. By methylsilicone fluid is meant a
composition containing two or more silicon atoms, all of which are bonded
by way of at least one oxygen atom to at least one other silicon atom and
at least one methyl radical, each silicon valence not satisfied by oxygen
being satisfied by a methyl radical. Representative methylsilicone fluids
found to be especially useful in accordance with the present invention are
hexamethyldisiloxane which has a boiling point of 99.5 degrees Centigrade
and the formula Me.sub.3 SiOSiMe.sub.3 ; octamethyltrisiloxane which has a
boiling point of 152 degrees Centigrade and the formula Me.sub.3
SiOMe.sub.2 SiOSiMe.sub.3 ; hexamethylcyclotrisiloxane which has a boiling
point of 133 degrees Centigrade and the formula [(Me.sub.2)SiO].sub.3 ;
octamethylcyclotetrasiloxane which has a boiling point of 171 degrees
Centigrade and the formula [(Me.sub.2)SiO].sub.4 ; and
decamethylcyclopentasiloxane which has a boiling point of 205 degrees
Centigrade and the formula [(Me.sub.2)SiO].sub.5.
These methylsilicone fluids may be used alone, or as mixtures in
combinations of two or more. Mixtures of the methylsilicone fluids will
result in a volatile material having an evaporating behavior different
from any one of the individual methylsilicone fluids.
The methylsilicone fluids and methods for their preparation are known in
the art.
Another type of volatile silicone in accordance with the present invention
is a volatile short chain linear alkylmethylsilicone fluid. The volatile
short chain linear alkylmethylsilicone fluid has the formula:
##STR1##
In the above formula, the integer represented by n has a value of five to
twelve. Preferably, n has a value of five to eight. Compounds most
preferred in terms of this invention are
3-hexyl-1,1,1,3,5,5,5,-heptamethyltrisiloxane and
3-octyl-1,1,1,3,5,5,5-heptamethyltrisiloxane. Measured at twenty-five
degrees Centigrade, these two preferred compounds have a viscosity of two
Centistokes and five Centistokes, respectively.
The alkylmethylsilicones of this invention can be produced by the reaction
of a linear siloxane having Si-H functionality in the chain with a slight
stoichiometric excess of an alkene CH.sub.2 .dbd.CHR in the presence of a
platinum on carbon catalyst. An alkylmethylsiloxane having the structure
shown above is produced.
The alkylmethylsilicones of this invention can also be produced by the
direct cohydrolysis of methylhydrogen dichlorosilane and trimethyl
chlorosilane. The reaction product is contacted with a slight
stoichiometric excess of an alkene CH.sub.2 .dbd.CHR in the presence of a
platinum on carbon catalyst, and an alkylmethylsiloxane having the
structure shown above is produced.
Batch production of the alkylmethylsilicones is conducted by adding the
reaction product to a non-agitated suspension of the catalyst in the
alkene at about sixty degrees Centigrade. Continuous production of the
alkylmethyl polysiloxanes is conducted by pumping a preheated solution of
a five percent stoichiometric excess of an alkene CH.sub.2 .dbd.CHR and
the reaction product through a packed column containing platinum on carbon
catalyst chips. The column will require provision for the removal of heat
because of the exothermic nature of the reaction.
The alkylmethylsilicones produced in accordance with the present invention
have been found to contain at most about 5 parts per million residual
alkene and about 99.95 percent alkylmethylsilicone product. No measurable
residual amount of platinum has been detected. The products are otherwise
colorless, odorless, clear and stable materials.
Yet another type of volatile silicone in accordance with the present
invention is a volatile short chain linear phenylmethylsilicone fluid. The
volatile short chain linear phenylmethylsilicone fluid has the formula:
##STR2##
This compound is 3-phenyl-1,1,1,3,4,4,4-heptamethyltrisiloxane.
The most preferred volatile silicone fluids according to the present
invention are decamethylcyclopentasiloxane (DMCPS) which has a molecular
weight of about 370, a refractive index of 1.40, and the formula
[(Me.sub.2)SiO].sub.5 ; the compound
3-hexyl-1,1,1,3,5,5,5-heptamethyltrisiloxane (HHMTS) which has a molecular
weight of about 306, and a refractive index of 1.41; and the compound
3-phenyl-1,1,1,3,5,5,5-heptamethyltrisiloxane (PHMTS)which has a molecular
weight of about 298 and a refractive index of 1.45. These compounds will
be referred to in the examples and in the table below as DMCPS, HHMTS, and
PHMTS, respectively, for the sake of convenience.
The paint remover composition of the invention contains 1 to 75 percent by
weight of acetone as the basic and main solvent ingredient; 1 to 10
percent by weight of water, preferably 5.0 to 7.5 percent by weight; 1 to
20 percent by weight of the volatile silicone fluid or a mixture of
volatile silicone fluids, but preferably about 15 to 20 percent by weight
of the volatile silicone fluid or fluid mixture: and other optional
adjuvants to 100 percent, such as coloring agents, perfumes and
fragrances, viscosity increasing agents, and emollient oils.
Colorants include any of the United States Government Food & Drug
Administration (FDA) certified inorganic and organic dyes and lakes such
as carmine, iron oxide, mica, titanium dioxide, ultramarine, zinc oxide,
bismuth oxychloride; and D & C Blue No. 1, D & C Orange No. 5, D & C Red
No. 6 Aluminum Lake, D & C Red No. 7 Calcium Lake, D & C Green No. 8, D &
C Red No. 17, FD & C Blue No. 1, FD & C Red No. 3, FD & C Yellow No. 6,
External D & C Violet No. 2, which are the CTFA adopted names of The
Cosmetic, Toiletry, and Fragrance Association, Washington, D.C.
Emollient oils which can be employed in the present invention include
mineral oil, peanut oil, sesame oil, avocado oil, coconut oil, cocoa
butter, almond oil, safflower oil, corn oil, cotton seed oil, castor oil,
olive oil, jojoba oil, paraffin oil, cod liver oil, palm oil, soybean oil,
wheat germ oil, linseed oil, and sunflower seed oil; fatty acid esters
such as isopropyl myristate, isopropyl palmitate, isopropyl stearate,
butyl stearate, cetyl stearate, diisopropyl adipate, isodecyl oleate,
diisopropyl sebacate, and lauryl lactate; fatty acids such as lauric,
myristic, palmitic, stearic, oleic, linoleic, and behenic, acid; fatty
alcohols such as lauryl, myristyl, cetyl, stearyl, isostearyl, oleyl,
ricinoleyl, erucyl, and 2-octyl dodecanol, alcohol; lanolin and its
derivatives such as lanolin, lanolin oil, lanolin wax, lanolin alcohols,
lanolin fatty acids, isopropyl lanolate, ethoxylated lanolin, and
acetylated lanolin alcohols such as ACETULAN.RTM., a trademark and product
of Amerchol Corporation, Edison. N.J.; hydrocarbons such as petrolatum and
squalane.
Fragrances which may be used include natural products such as ambergris,
benzoin, civet, clove, leaf oil, jasmine, mate', mimosa, musk, myrrh,
orris, sandalwood oil and vetivert oil; aroma chemicals such as amyl
salicylate, amyl cinnamic aldehyde, benzyl acetate, citronellol, coumarin,
geraniol, isobornyl acetate, ambrette, and terpinyl acetate; and the
various classic family perfume oils such as the floral bouquet family, the
oriental family, the chypre family, the woody family, the citrus family,
the canoe family, the leather family, the spice family, and the herbal
family.
Thickening agents which may be used include polyacrylates; sodium alignate;
gum arabic; guar gum; carboxyvinyl polymers; cellulose derivatives such as
methylcellulose, ethyl cellulose, hydroxypropyl methylcellulose,
hydroxyethylcellulose, hydroxypropylcellulose, and carboxymethylcellulose;
starch and starch derivatives such as hydroxyethylamylose and starch
amylose; polyvinyl alcohol; locust bean gum; vegetable gums; magnesium
aluminum silicate such as Veegum, a tradename of R. T. Vanderbilt Company,
Incorporated, Norwalk, Conn.; saccharide and saccharide derivatives such
as fructose, glucose, and PEG-120 methyl glucose dioleate: and the various
organically modified montmorillonite clays sold under the trademark
BENTONE.RTM. by Rheox Incorporated, Highstown, N.J., such as BENTONE.RTM.
38.
The paint remover compositions are prepared by simply mixing the various
components together. The paint remover compositions are used by applying
the composition to the surface to be cleaned, rubbing the composition into
the surface with cotton or paper towels until the surface below the
coating can be seen, and then wiping the surface clean of the coating and
the paint remover composition.
The invention will be further illustrated in more detail in the following
examples and tables.
Example I
Six (6) paint remover compositions were prepared by mixing together
acetone, water, and a volatile silicone fluid. These six compositions are
illustrated in Table I which shows the proportions of water and volatile
silicone in each paint remover. Each of the paint remover compositions in
Table 1 contained seventy-five percent by weight of acetone, which is the
maximum acetone content permitted under new and emerging VOC constraints
and targets in America. The remainder of the paint removal composition
consisted of water and the volatile silicone in the amounts indicated in
Table I.
TABLE I
______________________________________
Water DMCPS HHMTS PHMTS
Composition
(%) (%) (%) (%)
______________________________________
1 7.5 17.5 -- --
2 7.5 15.0 2.5 --
3 7.5 15.0 -- 2.5
4 5.0 20.0 -- --
5 5.0 15.0 5.0 --
6 5.0 15.0 -- 5.0
______________________________________
Example II
The six (6) paint remover compositions shown in Table I were evaluated as
paint removers. Two paints were employed. One paint was a consumer grade
commercially available nail polish enamel which was removed from the human
fingernails of volunteers. The volunteers evaluated the paint remover
compositions for ease of removal, appearance and feel of the nail surface,
following the removal of the coating from the nail surface. The other
paint evaluated was a non-crosslinked automotive acrylic enamel which was
removed from a primed steel surface. It was evaluated for ease of removal.
Example III
The six (6) paint remover compositions shown in Table I were evaluated as
paint removers by rubbing the coated surfaces in a transverse linear
motion with "Q-TIPS" until the substrate below the coated surface could
seen with the naked eye. In the case of the nail polish enamel, the entire
nail surface was cleaned free of enamel and then inspected for appearance
and feel after the elapse of about five minutes.
Based upon the evaluations of both surfaces, Compositions 5 and 6 provided
the best results, although the other four compositions functioned
adequately as paint removers. Compositions 2, 3, 5, and 6, showed no
whitening of the nail surface for the volunteers who had flexible nails.
With compositions 5 and 6, nail surfaces felt smooth and had the best
appearance. Composition 6 provided nail surface that were shiny.
Other variations and modifications may be made in the compounds,
compositions, and methods, described herein without departing from the
essential features and concepts of the present invention.
The forms of the invention described herein are exemplary only and are not
intended as limitations on the scope of the invention as defined in the
appended claims.
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Description  |
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