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| United States Patent | 5256191 |
| Link to this page | http://www.wikipatents.com/5256191.html |
| Inventor(s) | Thompson; John (81 Pine St., Medfield, MA 02052);
Ng; Kim H. (3 Annabell La., Franklin, MA 02038);
Ferguson; Edward J. (6 Forest Rd., Foxboro, MA 02035) |
| Abstract | Substantially non-toxic correction fluid compositions including an
opacifying pigment dispersed in a solution of a solvent, a siloxane and a
film-forming polymeric material. |
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Title Information  |
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| Publication Date |
October 26, 1993 |
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| Filing Date |
October 1, 1991 |
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| Parent Case |
CROSS REFERENCE TO RELATED APPLICATIONS
This application is a continuation-in-part of U.S. Ser. No. 07/606,961,
filed Oct. 31, 1990 now abandoned. |
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Title Information  |
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References  |
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U.S. References |
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| | Reference | Relevancy | Comments | Reference | Relevancy | Comments | 3276870
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Market Review  |
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Technical Review  |
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Claims  |
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We claim:
1. A correction fluid composition comprising an opacifying pigment
dispersed in a solution of a film-forming polymeric material and a
volatile organosiloxane in a volatile solvent and where the volume ratio
of the organosiloxane and the solvent provide an organosiloxane solvent
mixture in which the value of the (.delta..sub.p+h) of the mixture is
greater than about 2.0 cal.sup.1/2 cm.sup.-3/2 and less than about 7.35
cal.sup.1/2 cm.sup.-3/2 and the higher value is not exceeded at least
until about 90 percent of the mixture has evaporated.
2. A correction fluid of claim 1 wherein said solvent has a
(.delta..sub.p+h) value between 2.5 to about 12.4 cal.sup.1/2 cm.sup.-3/2.
3. A correction fluid of claim 1 where in said (.delta..sub.p+h) of said
mixture is greater than about 2.3 cal.sup.1/2 cm.sup.-3/2.
4. A correction fluid composition of claim 3 wherein the values of the
solubility parameter components of said mixture are greater than about 1.5
and less than about 3.6 cal.sup.1/2 cm.sup.-3/2 for .delta..sub.p and
greater than about 1.8 and less than about 6.4 cal.sup.1/2 cm.sup.-3/2
for .delta..sub.h.
5. A correction fluid of claim 3 where the solvent has a solubility
parameter between about 7.2 to about 14 cal.sup.1/2 cm.sup.-3/2 and a
(.delta..sub.p+h) value between about 3.5 to about 12.4 cal.sup.1/2
cm.sup.-3/2.
6. A correction fluid of claim 5 where the concentration of opacifying
pigment is between about 30 to about 60 percent by weight of the total
weight of the composition, the concentration of organosiloxane is between
about 10 to about 40 percent by weight, the concentration of polymeric
material is between about 3 to about 10 percent by weight and the
concentration of solvent is between about 10 to about 30 percent by
weight.
7. A correction fluid of claim 6 where the concentration of opacifying
pigment is between about 45 to about 55 percent by weight of the total
weight of the composition, the concentration of organosiloxane is between
about 15 to about 35 percent by weight, the concentration of polymeric
material is between about 5 to about 8 percent by weight and the
concentration of solvent is between about 12 to about 25 percent by
weight.
8. A correction fluid of claim 7 where the organosiloxane conforms to the
following formulae:
##STR3##
where each R is hydrogen or alkyl having from 1-3 carbon atoms, and m is
0, 1, or 2 and n is 4 or 5.
9. A correction fluid of claim 8 where the polymeric material is an acrylic
polymer having a molecular weight between 50,000 and 500,000.
10. A correction fluid of claim 9 where the solvent is a volatile alcohol,
ketone or ester or mixtures of these.
11. A correction fluid of claim 10 where the organosiloxane is
hexamethyldisiloxane or octamethylcyclotetrasiloxane or mixtures of these.
12. A correction fluid of claim 11 where the polymeric material is methyl
methacrylate, butyl methacrylate, isobutyl methacrylate or mixtures of
these.
13. A correction fluid of claim 12 where the solvent is ethyl alcohol,
isopropyl alcohol, methyl ethyl ketone, ethyl acetate or mixtures of
these.
14. A correction fluid of claim 13 where the organosiloxane is
hexamethyldisiloxane, the polymeric material is an isobutylmethacrylate
and the solvent is isopropyl alcohol.
15. A correction fluid of claim 13 where the organosiloxane is
octamethylcyclotetrasiloxane, the polymeric material is an
isobutylmethacrylate and the solvent is isopropyl alcohol.
16. A correction fluid of claim 1 where the mixture of said solvent and
said organosiloxane has a .delta..sub.p value of greater than about 1.6.
17. A correction fluid of claim 16 where the solvent comprises a terpene.
18. A method for producing a corrective coating on the surface of a
substrate, said method comprising the steps of:
a. providing a composition including an opacifying pigment dispersed in a
solution of a film-forming polymeric material and a volatile
organosiloxane in a volatile solvent and where the volume ratio of the
organosiloxane and the solvent provide an organosiloxane solvent mixture
in which the value of the (.delta..sub.p+h) of the mixture is greater than
about 2.0 cal.sup.1/2 cm.sup.-3/2 and less than about 7.35 cal.sup.1/2
cm .sup.-3/2 and the higher value is not exceeded at least until about 90
percent of the mixture has evaporated,
b. applying said composition to a marking on the surface of a substrate to
cover said marking;
c. allowing said volatile organosiloxane and said volatile solvent to
evaporate to form a film comprising said film-forming polymeric material
covering said marking.
19. The method of claim 18 wherein said solvent has a (.delta..sub.p+h)
value of between about 2.5 to about 12.4 cal.sup.1/2 cm.sup.-3/2.
20. The method of claim 18 where in said composition provided said
(.delta..sub.p+h) of said mixture is greater than about 2.3 cal.sup.1/2
cm.sup.-3/2.
21. The method of claim 20 where in said composition provided the values of
the solubility parameter components of said mixture are greater than about
1.5 and less than about 3.6 cal.sup.1/2 cm.sup.-3/2 for .delta..sub.p and
greater than about 1.8 and less than about 6.4 cal.sup.1/2 cm.sup.-3/2
for .delta..sub.h.
22. The method of claim 20 where in said composition provided said volatile
solvent has a solubility parameter between about 7.2 to about 14
cal.sup.1/2 cm.sup.-3/2 and a (.delta..sub.p+h) value between about 3.5
to about 12.4 cal.sup.1/2 cm.sup.-3/2.
23. The method of claim 20 where in said composition provided the
concentration of opacifying pigment is between about 30 to about 60
percent by weight of the total weight of the composition, the
concentration of organosiloxane is between about 10 to about 40 percent by
weight, the concentration of polymeric material is between about 3 to
about I0 percent by weight and the concentration of solvent is between
about 10 to about 30 percent by weight.
24. The method of claim 20 where in said composition provided the
concentration of opacifying pigment is between about 45 to about 55
percent by weight of the total weight of the composition, the
concentration of organosiloxane is between about 15 to about 35 percent by
weight, the concentration of polymeric material is between about 5 to
about 8 percent by weight and the concentration of solvent is between
about 12 to about 25 percent by weight.
25. The method of claim 20 wherein the organosiloxane conforms to the
following formulae:
##STR4##
where each R is hydrogen or alkyl having from 1-3 carbon atoms, and m is
0, 1, or 2 and n is 4 or 5.
26. The method of claim 20 where in said composition provided the polymeric
material is an acrylic polymer having a molecular weight between 50,000
and 500,000.
27. The method of claim 20 where in said composition provided the solvent
is a volatile alcohol, ketone or ester or mixtures of these.
28. The method of claim 20 where in said composition provided the
organosiloxane is hexamethyldisiloxane or octamethylcyclotetrasiloxane or
mixtures of these.
29. The method of claim 20 where in said composition provided the polymeric
material is methyl methacrylate, butyl methacrylate, isobutyl methacrylate
or mixtures of these.
30. The method of claim 20 where in said composition provided the solvent
is ethyl alcohol, isopropyl alcohol, methyl ethyl ketone, ethyl acetate or
mixtures of these.
31. The method of claim 20 where in said composition provided the
organosiloxane is hexamethyldisiloxane, the polymeric material is an
isobutylmethacrylate and the solvent is isopropyl alcohol.
32. The method of claim 20 where in said composition provided the
organosiloxane is octamethylcyclotetrasiloxane, the polymeric material is
an isobutylmethacrylate and the solvent is isopropyl alcohol.
33. The method of claim 18 where said solvent comprises a non-polar
solvent.
34. The method of claim 33 where in said composition provided the solvent
comprises a terpene.
35. A correction fluid composition comprising an opacifying pigment
dispersed in a solution of a volatile solvent, a volatile organosiloxane
and a film-forming polymeric material, said composition having a drying
time of less than 60 seconds.
36. The correction fluid of claim 35 where the concentration of opacifying
pigment is between about 30 to about 60 percent by weight of the total
weight of the composition, the concentration of organosiloxane is between
about 10 to about 40 percent by weight, the concentration of polymeric
material is between about 3 to about 10 percent by weight and the
concentration of solvent is between about 10 to about 30 percent by
weight.
37. The correction fluid of claim 35, wherein said solvent is a terpene.
38. A correction fluid of claim 36 where the concentration of opacifying
pigment is between about 45 to about 55 percent by weight of the total
weight of the composition, the concentration of organosiloxane is between
about 15 to about 35 percent by weight, the concentration of polymeric
material is between about 5 to about 8 percent by weight and the
concentration of solvent is between about 12 to about 25 percent by
weight.
39. A correction fluid of claim 36 where the solvent comprises a non-polar
solvent.
40. A correction fluid of claim 35 where the organosiloxane conforms to the
following formulae:
##STR5##
where each R is hydrogen or alkyl having from 1-3 carbon atoms, and m is
0, 1, or 2 and n is 4 or 5.
41. A correction fluid of claim 35 where the polymeric material is an
acrylic polymer having a molecular weight between 50,000 and 500,000.
42. A correction fluid of claim 35 where the solvent is a volatile alcohol,
ketone or ester or mixtures of these.
43. A correction fluid of claim 35 where the organosiloxane is
hexamethyldisiloxane or octamethylcyclotetrasiloxane or mixtures of these.
44. A correction fluid of claim 43 where the polymeric material is methyl
methacrylate, butyl methacrylate, isobutyl methacrylate or mixtures of
these.
45. A correction fluid of claim 44 where the solvent is ethyl alcohol,
isopropyl alcohol, methyl ethyl ketone, ethyl acetate or mixtures of
these.
46. A correction fluid of claim 45 where the organosiloxane is
hexamethyldisiloxane, the polymeric material is an isobutylmethacrylate
and the solvent is isopropyl alcohol.
47. A correction fluid of claim 45 where the organosiloxane is
octamethylcyclotetrasiloxane, the polymeric material is an
isobutylmethacrylate and the solvent is isopropyl alcohol.
48. A method for providing a corrective coating, suitable for receiving a
corrective marking, on the surface of a paper substrate, said method
comprising the steps of:
a. providing a composition comprising an opacifying pigment dispersed in a
solution of a volatile polar solvent, a volatile organosiloxane and a
film-forming polymeric material, said composition having a drying time of
less than 60 seconds;
b. applying said composition to a marking on the surface of a paper
substrate to cover said marking; and
c. allowing said volatile organosiloxane and said volatile solvent to
evaporate to form a film comprising said film-forming polymeric material
covering said marking.
49. The method of claim 48, comprising the additional step of applying a
corrected marking to said film.
50. The method of claim 49 where said solvent comprises a polar solvent.
51. A correction fluid composition comprising an opacifying agent dispersed
in a solution comprising a film-forming polymeric material and a volatile
terpene solvent, said film-forming polymeric material being capable of
forming a durable film on a paper substrate at room temperature within 60
seconds after said correction fluid composition is applied to said paper
substrate.
52. The correction fluid composition of claim 51 where said terpene is a
paramenthadiene.
53. The correction fluid composition of claim 51, wherein said solution
further comprises volatile organosiloxane.
54. A correction fluid of claim 53 where the concentration of opacifying
pigment is between about 30 to about 60 percent by weight of the total
weight of the composition, the concentration of organosiloxane is between
about 10 to about 40 percent by weight, the concentration of polymeric
material is between about 3 to about 15 percent by weight and the
concentration of terpene is between about 5 to about 30 percent by weight.
55. The correction fluid composition of claim 54 where said terpene is
paramenthadiene.
56. A method for providing a corrective coating on the surface of a paper
substrate, said method comprising the steps of:
a. providing a composition comprising an opacifying pigment dispersed in a
solution that includes a volatile terpene solvent and a film-forming
polymeric material;
b. applying said composition to a marking on the surface of a paper
substrate to cover said marking; and
c. allowing said volatile terpene to evaporate to form a film comprising
said film-forming polymeric material covering said marking.
57. The method of claim 56, comprising the additional step of applying a
corrected marking to said film.
58. The correction fluid of claim 51 wherein said opacifying pigment is
titanium dioxide. |
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Claims  |
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Description  |
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BACKGROUND OF THE INVENTION
The invention relates to novel, improved correction fluid compositions.
More precisely, this invention relates to novel, improved correction fluid
compositions which have reduced potential for adverse effects on the
environment and on health.
Correction fluid compositions (or correction fluids) for correcting
handwritten, typewritten or photocopy markings on papers are known
products of commerce and their performance characteristics are well
defined. Essential performance characteristics include the ability to
provide a film or coalesced residue on drying which can both effectively
cover erroneous markings on a paper surface and receive a corrected
marking. Preferably, the film covering the marking should be strongly
bonded to the paper surface and should also be sufficiently flexible so
that the film will not be removed under normal conditions of handling.
Additionally, the correction fluid should not interact with the marking to
cause excessive discoloration of the resulting film (bleeding). Another
important performance characteristic involve the drying rate of the
composition which should be as rapid as possible so that corrections can
be made relatively quickly. Normally, commercial correction fluids form
films which are sufficiently dry to receive a corrected marking in about
30-40 seconds. Other desired performance characteristics include good
storage stability coupled with flow and viscosity characteristics which
permit easy and even application of the fluid. Details relating to known
correction fluids can be found in U.S. Pat. Nos. 3,276,870, 3,674,729;
3,997,498; 4,165,988 and 4,654,081.
As evidenced by the above-listed Patents, halogenated hydrocarbons have
been the solvents of choice for correction fluid compositions. Halogenated
hydrocarbon solvents presents special advantages primarily because they
have evaporation rates which provide correction fluids which can dry
rapidly and completely. Additionally, they do not interact with
typewritten markings to cause unacceptable bleeding. Also, they can
effectively dissolve those film forming polymeric materials which provide
durable but flexible films without causing excessive cockling or
distortion of paper surfaces. Despite their recognized advantages when
used as correction fluid solvents, the use of halogenated hydrocarbon
solvents has become a matter of increased concern primarily because of
their adverse effect on the environment (stratospheric ozone depletion)
and also because of their potential adverse effect on health through
solvent abuse. Accordingly, the elimination of halogenated hydrocarbon
solvents from correction fluids has become a primary objective for the art
and significant efforts have been directed to the development of
correction fluids free of halogenated hydrocarbon solvents.
Commercially available halogenated hydrocarbon-free correction fluids
developed by the art have not proved to be completely satisfactory
substitutes for correction fluids based on halogenated hydrocarbon
solvents. Actually, only a relatively few non-halogenated hydrocarbon
solvents have the desired combination of performance characteristics
needed to qualify for use as correction fluid solvents. For example,
heptane or cyclohexane and substituted derivatives thereof provide
acceptable non-bleeding performance characteristics coupled with the
capability to dissolve polymeric materials which provide the desired
durable but flexible films. Moreover, non-halogenated hydrocarbon solvents
are not entirely free of adverse effects on the environment and/or on
health. Aqueous based correction fluids have also been developed and such
fluids do not present any significant threat to the environment or to
health. However, they can interact with aqueous based ink markings to
cause unwanted bleeding and they also tend to cockle the surface of the
paper carrying the marking. Accordingly, a need remains for the
development of a halogenated hydrocarbon-free correction fluid which
provides a combination of performance characteristics substantially
similar to those provided by correction fluids based on halogenated
hydrocarbon solvents. This invention is addressed to that need and
provides an effective response to the need.
SUMMARY OF THE INVENTION
Correction fluid compositions of the invention are substantially non-toxic,
rapid drying, film forming compositions.
In one aspect, the invention features a correction fluid composition that
includes an opacifying pigment dispersed in a solution. The solution
includes a volatile organosiloxane, an additional volatile solvent, and a
film-forming polymeric material. The volume ratio of the organosiloxane
and the solvent provides a mixture in which the (.delta..sub.p+h) of the
mixture is greater than about 2.0 cal.sup.1/2 cm.sup.-3/2 (preferably 2.3
cal.sup.1/2 cm.sup.-3/2), and less than about 7.35 cal.sup.1/2 cm and the
latter value is not exceeded at least until about 90% of the mixture has
evaporated.
In another aspect, the invention features a correction fluid composition
that includes an opacifying agent dispersed in a solution of a volatile
organosiloxane, a second volatile solvent, and a film-forming polymeric
material. The composition has a drying time of less than 60 seconds.
Preferred organosiloxanes are those having the following formulae:
##STR1##
where each R is hydrogen or alkyl having from 1-3 carbon atoms, and m is
0, 1, or 2 and n is 4 or 5. Examples of the preferred organosiloxanes
include hexamethyldisiloxane and octamethylcyclotetrasiloxane.
Preferred solvents include polar solvents like ethyl alcohol, isopropyl
alcohol, methyl ethylketone, and ethyl acetate. Other preferred solvents
include those having a (.delta..sub.p+h) value between about 2.5 and 12.4
cal.sup.1/2 cm.sup.-3/2. Preferably, the .delta..sub.p value of the
organosiloxane-solvent mixture is greater than about 1.5 and less than
about 3.6 cal.sup.1/2 cm.sup.-3/2, and the .delta..sub.h value greater
than about 1.3 and less than about 6.4 cal.sup.1/2 cm.sup.-3/2.
Preferred film-forming polymeric materials include acrylic polymers, such
as methyl methacrylate, butyl methacrylates, and isobutyl methacrylate,
having a molecular weight of between 50,000 and 500,000.
In another aspect, the invention features a correction fluid including an
opacifying agent dispersed in a solution including a film-forming
polymeric material and a terpene e.g. a paramenthadiene solvent.
Preferably the solution also includes a volatile organosiloxane.
Correction fluid compositions of the invention have excellent drying times
as measured in accordance with the procedure described in detail later.
The correction fluids are applied to a marking to be corrected such as by
a brush or pen dispenser and do not undergo significant interaction with
the marking to cause unacceptable discoloration (bleeding) of the fluid.
On drying, the applied fluid provides a film or coalesced residue which
can cover the marking and can receive a corrected marking. Additionally,
the coalesced residue is durable and flexible and does not cockle or
otherwise distort the paper surface.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
Those skilled in the art know that a variety of pigments can be included in
a dispersion of a solvent and a film forming polymeric materials to
provide correction fluid compositions. Substantially all correction fluid
compositions include titanium dioxide as the opacifying pigment(s) to
provide the basic white color which can be toned to provide a correction
fluid composition closely corresponding to the color of the paper to which
the composition is intended to be applied. Suitable titanium dioxide
pigments include commercially available rutile titanium dioxides and
anatase titanium dioxides or blends or mixtures of these which preferably
have an average particle size between about 0.2 to about 0.4 microns and
an average oil absorption of about 14 lbs. oil/100 lbs. pigment to about
36 lbs./100 lbs. The amount of titanium dioxide included in the
composition can vary depending primarily on the degree of coverage
desired. However, amounts between about 30 to about 60 percent by weight
titanium dioxide based on the total weight of the composition are
generally suitable. Other opacifying pigments may be used either alone but
preferably in combination with the titanium dioxide. Such pigments include
zinc sulfide, zinc oxide, and basic lead carbonate or sulphate. Colored
pigments may also be used for matching the color of the correction
composition to the color of the paper to which the composition is applied.
Siloxanes suitable in the practice of the invention are volatile, low
viscosity, open or closed siloxane dimers, trimers, tetramers or
pentamers. Preferred siloxanes reduce surface tension and promote leveling
and are clear liquids which are essentially odorless, non-toxic,
non-greasy and non-stringing and conform to the following formulae:
##STR2##
where each R is hydrogen or alkyl having from 1 to 3 carbon atoms and m is
0, 1 or 2 and n is 4 or 5. Particularly preferred siloxanes are alkyl
substituted siloxanes and especially hexamethyldisiloxane and
octamethylcyclotetrasiloxane. These especially preferred siloxanes are
normally used in amounts between about 10 to about 40 percent by weight
siloxane based on the total weight of the correction fluid composition.
Polymeric film forming materials suitable for use in correction fluid
compositions of the invention are substantially completely soluble in the
selected solvent mixture at room temperature. Particularly useful
polymeric film forming materials are the medium to hard acrylic polymers
such as methyl, butyl and isobutyl methacrylates having molecular weights
between about 50,000 to about 500,000. Other suitable polymeric materials
include vinyl polymers such as, copolymers of vinyl acetate and vinyl
toluene or mixtures of these with the acrylic polymers. The amount of
polymeric film forming material can vary but amounts between about 3 to
about 10 percent by weight polymeric material based on the total weight of
the correction fluid composition are normally suitable.
The amount of solvent(s) used in combination with the siloxane(s) is a
critical feature of correction fluids of the present invention. If the
amount of solvent is too low, the polymeric film forming material may not
be sufficiently dissolved. On the other hand, if the amount of solvent is
too high, the solvent may interact excessively with the marking producing
unacceptable bleed. In accordance with the present invention, the
solubility parameter(s) of the solvent(s)/siloxane(s) mixture is used to
determine the appropriate amount of solvent needed to effectively dissolve
the polymeric film forming material and provide minimal bleed.
Essentially, the solubility parameter of a liquid is a function of three
components: the dispersion component (.delta..sub.d), the polar component
(.delta..sub.p) and the hydrogen bonding component (.delta..sub.h). These
components are related to the solubility parameter by the following
equation:
##EQU1##
(the solubility parameter values are expressed in cal.sup.1/2 cm.sup.-3/2
units)
The polar and hydrogen bonding components of the solubility parameter can
be combined in the following equation:
##EQU2##
Accordingly, the solubility parameter of a selected solvent/siloxane
mixture can be determined by the volume fraction .phi. of each component
of the mixture as follows:
.delta..sub.d (mixture)=(.phi..delta..sub.d) siloxane+(.phi..delta..sub.d)
polar solvent
.delta..sub.p (mixture)=(.phi..delta..sub.p) siloxane+(.phi..delta..sub.p)
polar solvent
.delta..sub.h (mixture)=(.phi..delta..sub.h) siloxane+(.phi..delta..sub.h)
polar solvent
The solubility parameter components for the siloxane are calculated
according to the method in A.F.M. Barton's CRC Handbook of Solubility
Parameters pg. 82-87 (CRC Press 1983) assuming the same value
for=Si=and=C=. The solubility parameters for the solvents are obtained
from Polymer Handbook, Second Edition, Part IV, page 348, Editors Brandrup
& Immergut, Pub.: Wiley & Son 1975; to the extent the solubility parameter
for particular solvents are not listed in the Polymer Handbook, they can
be calculated according to the methods described in A.F.M. Barton's
Handbook.
The following illustrates the manner of determining the solubility
parameter of a 50/50 volume mixture of hexamethyldisiloxane (HMDS) and
ethanol. All values are expressed in cal.sup.1/2 cm.sup.-3/2 units.
______________________________________
Component Solubility Parameter
Liquid .delta..sub.d
.delta..sub.p
.delta..sub.h
(.delta.)
(.delta..sub.p+h)
______________________________________
HMDS 8.67 1.47 1.81 6.1 --
Ethanol 7.73 4.30 9.50 12.98
10.4
50/50 6.70 2.89 5.60 9.23 6.3
Mixture
______________________________________
Based on bleed testing of a variety of siloxane/polar solvent mixtures we
have found that siloxane/polar solvent mixtures in which the
(.delta..sub.p+h) value of the solubility parameter components of the
mixture are less than about 7.35 cal.sup.1/2 cm.sup.-3/2 provide minimal
bleed. Siloxane/solvent mixtures especially preferred for minimized bleed
are those in which the .delta..sub.p and .delta..sub.h values of the
solubility parameter components are less than about 3.6 and about 6.4
cal.sup.1/2 cm.sup.-3/2 respectively. Additionally, effective dissolution
of the polymeric film forming material(s) is achieved in siloxane/solvent
mixtures in which the (.delta..sub.p+h) value of the solubility parameter
components is greater than about 2.0, more preferably 2.3, cal.sup.1/2
cm.sup.-3/2 Especially effective dissolution of the polymeric film forming
material(s) is achieved when the values of the .delta..sub.p and
.delta..sub.h solubility parameter components are greater than about 1.5
and 1.8 cal.sup.1/2 cm.sup.-3/2 respectively. Furthermore, the value of
(.delta..sub.p+h) should not exceed about 7.35 cal.sup.1/2 cm.sup.-3/2
and the values of the .delta..sub.p and .delta..sub.h solubility parameter
components of the mixture should not exceed about 3.6 and 6.4 cal.sup.1/2
cm.sup.-3/2 respectively until about 90% of the solvent mixture has
evaporated in order to minimize bleed. If the evaporation rate of the
solvent is slower than the evaporation rate of the siloxane, a non-polar,
slow evaporating solvent such as mineral spirits may be added to the
mixture to maintain the values of (.delta..sub.p+h), .delta..sub.p and
.delta..sub.h Within this specified range.
Preferred polar solvents are those having a solubility parameter between
about 7.2 to about 14 cal.sup.1/2 cm.sup.-3/2 and where the value of
(.delta..sub.p+h) of the solvent is between about 3.5 to about 12.4
cal.sup.1/2 cm.sup.-3/2. Especially preferred polar solvents have boiling
points between about 60.degree. to about 110.degree. C. and include
volatile alcohols, ketones and esters such as ethyl and isopropyl alcohol,
methyl ethyl ketone and ethyl acetate. The amount of polar solvent used in
the siloxane/solvent mixtures should be sufficient to provide a correction
fluid having free flow characteristics so that the fluid can be applied to
a marking with a brush and provide a relatively thin film covering the
marking. Representative suitable amounts of the preferred solvents are
between about 10 to about 30 percent by weight solvent based on the total
weight of the correction fluid composition.
In addition to the four basic components of the correction fluid
compositions, i.e., the opacifying pigment, siloxane, polymeric film
forming material and solvent the compositions may include a plasticizer,
which is preferably soluble in the solvent. The plasticized be used to
reduce embrittlement and improve adhesion and flexibility of the film
formed by the composition thereby minimizing chipping off or flaking of
the film. Suitable specific plasticizers include di-(2-ethylhexyl)
phthalate, dioctyl phthalate, dibutyl phthalate, low molecular weight
polystyrene, mineral oil, tricresyl phosphate, and castor oil. Amounts of
plasticizer between about 0 to 5 parts by weight are normally employed.
However, somewhat more or less can be used if needed or desired.
A dispersing agent(s) or surfactant may also be employed in the correction
compositions of the present invention if needed to stabilize the
composition or to assure that the covering power provided by the
pigment(s) is substantially evenly distributed throughout the dispersion.
Suitable commercially available dispersing agents include those sold under
the trade names NUOSPERSE 700 and AEROSOL OTS sold by Huls America Inc.
and American Cyanamide Co. respectively, and the amounts used can vary but
amounts between 0 to about 5 percent by weight of the composition are
normally employed.
Other additive materials which can be included in the correction
compositions are toners such as a selected grade of carbon black to obtain
the desired shade of white. Other toners such as colored pigments or dyes
can be suitably employed to obtain compositions of desired colors for use
on correspondingly colored papers. Additionally, effective amounts of
thickening agents can be employed as thixotropic agents to control
settling of the dispersed materials. Amounts of thickening agents between
about 0 to about 5 percent by weight are normally suitable.
Representative correction fluid compositions of the present invention are
set out in Table 1 below.
TABLE 1
______________________________________
Preferred
Range Range
Ingredient (% by wt.)
(% by wt.)
______________________________________
Pigment(s) 30-60 45-55
Siloxane(s) 10-40 15-35
Polymeric Material(s)
3-10 5-8
Solvent(s) 10-30 12-25
Plasticizer(s) 0-5 0-2
Dispersing Agent(s)
0-5 0-2
Thickening Agent(s)
0-5 0-2
______________________________________
Correction fluid compositions of the invention can be prepared by agitating
or shaking a mixture of the siloxane, the film forming polymeric material
and the solvent until the polymeric material is dissolved. The opacifying
pigment and other ingredients such as plasticizer, dispersing agent and
the thickening agent are then added to the dispersion of siloxane in the
polymeric material/solvent solution and the ingredients are subjected to
high speed agitation or shaking to provide the final correction fluid
composition.
The invention as well as details relating to the invention will be more
fully appreciated by reference to the following illustrative, non-limiting
Example which describes preferred correction fluid compositions of the
invention and the manner for preparing the correction fluid compositions.
EXAMPLE
The correction fluid compositions of this Example were prepared in
accordance with the following procedure:
1. Add siloxane, polymeric film forming material and solvent to a can (500
mls.)
2. Cover can and shake on paint shaker until polymeric material is
dissolved (1 hour).
3 Add titanium dioxide pigment, plasticizer and/or dispersants to the step
2 dispersion.
4. Mix the ingredients at high speed (1000-1500 rpm) for ten minutes.
5. Place step 4 dispersion in can and add enough glass beads to the
dispersion so that the glass beads represent about one-third of the volume
of the dispersion.
6. Cover the can and shake on paint shaker until the pigment fineness
achieves a grind of 4. (20 minutes).
7. Filter out beads and, if needed, add small amount of colorant to adjust
the tint of the fluid.
8. Add siloxane and/or solvent to adjust % of non-volatiles (optional).
______________________________________
PERCENT BY WEIGHT
INGREDIENT 1 2 3 4 5
______________________________________
Titanium Dioxide.sup.1
51.65 52.09 50.84
50.34 50.17
Hexamethyldisiloxane
-- -- 16.11
15.62 7.85
Octamethylcyclo-
15.79 15.58 -- -- 7.85
tetrasiloxane
Polymeric Material.sup.2
7.06 7.12 6.95
Polymeric Material.sup.3
-- -- -- 6.88 6.86
Isopropanol (Solvent)
23.68 23.78 24.25
24.43 23.55
Methylethyl Ketone
-- 23.28 -- -- --
(Solvent)
Plasticizer.sup.4
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