U.S. patent application number 14/714545 was filed with the patent office on 2015-09-10 for process for making polymers having nanostructures incorporated into the matrix of the polymer.
The applicant listed for this patent is PPG INDUSTRIES OHIO, INC.. Invention is credited to Mehran Arbab, Songwei Lu, Thomas G. Rukavina.
Application Number | 20150252169 14/714545 |
Document ID | / |
Family ID | 35385804 |
Filed Date | 2015-09-10 |
United States Patent
Application |
20150252169 |
Kind Code |
A1 |
Lu; Songwei ; et
al. |
September 10, 2015 |
PROCESS FOR MAKING POLYMERS HAVING NANOSTRUCTURES INCORPORATED INTO
THE MATRIX OF THE POLYMER
Abstract
The present invention is directed toward a polymer and a method
for making a polymer that has nanostructures incorporated into the
matrix of the polymer. The method of the invention involves the
following steps; mixing a precursor solution for the polymer with a
precursor for the nanostructures to form a mixture; forming
nanostructures in the mixture from the precursor of the
nanostructures; and forming a polymer from the precursor solution
of the polymer so that the nanostructures are incorporated into the
polymer matrix.
Inventors: |
Lu; Songwei; (Wexford,
PA) ; Rukavina; Thomas G.; (New Kensington, PA)
; Arbab; Mehran; (Pittsburgh, PA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
PPG INDUSTRIES OHIO, INC. |
Cleveland |
OH |
US |
|
|
Family ID: |
35385804 |
Appl. No.: |
14/714545 |
Filed: |
May 18, 2015 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
13455609 |
Apr 25, 2012 |
9045606 |
|
|
14714545 |
|
|
|
|
10932641 |
Sep 1, 2004 |
8178615 |
|
|
13455609 |
|
|
|
|
Current U.S.
Class: |
524/784 ;
524/783; 524/786 |
Current CPC
Class: |
C08K 2003/2231 20130101;
C08K 2003/2241 20130101; C08K 2003/2244 20130101; C08J 3/205
20130101; C08K 3/22 20130101; C08K 3/2279 20130101; C08K 3/22
20130101; C08L 29/14 20130101; C08K 3/2279 20130101; C08L 69/00
20130101; C08L 29/14 20130101; C08K 3/22 20130101; C08L 31/00
20130101; C08K 2003/2227 20130101; C08K 3/22 20130101; C08L 69/00
20130101; C08L 31/00 20130101; B82Y 30/00 20130101 |
International
Class: |
C08K 3/22 20060101
C08K003/22 |
Claims
1. A polymer having a matrix that has nanostructures incorporated
into the matrix of the polymer formed by a method, comprising; a.
mixing a precursor solution for the polymer with a precursor for
the nanostructures to form a mixture, wherein the mixture consists
essentially of the precursor solution for the polymer and the
precursor for the nanostructures; b. forming nanostructures in the
mixture from the precursor of the nanostructures wherein the
nanostructures are surrounded by the polymer precursor when they
are formed; and c. forming a polymer from the precursor solution of
the polymer so that the nanostructures are incorporated into the
polymer matrix, wherein the nanostructures incorporated into the
polymer matrix are in the range of 1 nm to 1,000 nm in length, and
do not agglomerate to the extent the performance of the polymer is
compromised.
2. The polymer according to claim 1, wherein the polymer includes
nanostructures having a concentration in the polymer matrix ranging
from 0.1% to 90% based on volume.
3. The polymer according to claim 1, wherein the polymer includes
nanostructures selected from spherical, polyhedral cubic,
triangular, pentagonal, diamond shaped, needle shaped, rod shaped,
and disc shaped,
4. The polymer according to claim 1, wherein the polymer includes
nanostructures having an aspect ratio of 1:1 to 1:1,000.
5. A polymer having a matrix that has nanostructures incorporated
into the matrix of the polymer, comprising: a polymer matrix; and
nanostructures incorporated into the polymer matrix, wherein the
nanostructures incorporated into the polymer matrix are in the
range of 1 nm to 1,000 nm in length, and do not agglomerate to the
extent the performance of the polymer is compromised.
6. The polymer of claim 5, wherein the polymer comprises a
polyvinyl acetal resin.
7. The polymer of claim 5, wherein the polymer comprises poly
[bis(diethylene glycol) diallylcarbonate].
8. The polymer of claim 5, wherein the polymer comprises an
aliphatic polyurethane.
9. The polymer of claim 5, wherein the nanostructures are similarly
charged.
10. The polymer of claim 5, wherein the nanostructures in the
polymer matrix range from 3% to 85% based on volume.
11. The polymer of claim 5, wherein the nanostructures are selected
from the group consisting of indium tin oxide (ITO), antimony tin
oxide (ATO), titania, alumina, and zirconia.
12. The polymer of claim 5, wherein the polymer has an average
molecular weight greater than 70,000 as measured by size exclusion
chromatography using low angle laser light scattering.
13. A polymer having a matrix that has nanostructures incorporated
into the matrix of the polymer, comprising: a polymer matrix
comprising at least one polymer selected from the group consisting
of a polyvinyl acetal resin, poly [bis(diethylene glycol)
diallylcarbonate], and an aliphatic polyurethane; and
nanostructures incorporated into the polymer matrix, wherein the
nanostructures are similarly charged, wherein the nanostructures in
the polymer matrix range from 3% to 85% based on volume, and
wherein the nanostructures are selected from the group consisting
of indium tin oxide (ITO), antimony tin oxide (ATO), titania,
alumina, and zirconia.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] The present patent application is a continuation of and
claims priority under 35 U.S.C. .sctn.121 to U.S. patent
application Ser. No. 13/455,609, filed Apr. 25, 2012, which is a
divisional of and claims priority under 35 U.S.C. .sctn.121 to U.S.
patent application Ser. No. 10/932,641 (now U.S. Pat. No.
8,178,615), filed Sep. 1, 2004, both of which applications are
incorporated herein by reference in their entireties.
FIELD OF INVENTION
[0002] The present invention relates to a process for making
polymers having nanostructures incorporated into the matrix of the
polymer and to the polymers themselves.
BACKGROUND OF THE INVENTION
[0003] Products such as aerospace and automotive transparencies,
optical lenses, coating compositions, fiberglass surface modifiers,
etc. are made of various polymers. In an attempt to make better
products, scientists and engineers have tried to optimize the
performance properties of the polymers used to make the products.
Various techniques have been proposed for optimizing the
performance properties of polymers.
[0004] For example, scientists and engineers have attempted to
incorporate nanostructures into polymer matrices to modify the
performance properties of a polymer. Because nanostructures have
significantly different physical properties from corresponding bulk
material and the polymer matrix, incorporating the nanostructures
changes the performance properties of the polymer. Nanostructures
have been incorporated into polymer matrices to improve the thermal
stability of polymers and to decrease the chemical activity of
polymers.
[0005] Conventionally, nanostructures have been incorporated into
the matrix of a polymer by taking pre made nanostructures and
dispersing them into the polymer solution. Typically, the
dispersing step includes several other steps such as modifying the
surface, mixing, stirring, heating, milling, etc. The conventional
process is inefficient due to the multiple steps involved and tends
to produce polymers in which the nanostructures agglomerate. When
nanostructures agglomerate in the polymer, the nanostructures can
effectively become regular sized particles and the desired effect
of incorporating the nanostructures is reduced.
[0006] The present invention provides an improved process for
making a polymer having nanostructures incorporated into the matrix
of the polymer. Polymers produced according to the present
invention undergo reduced nanostructure agglomeration.
SUMMARY OF THE INVENTION
[0007] In a non-limiting embodiment, the present invention is a
method for making a polymer that has nanostructures incorporated
into the matrix of the polymer comprising: mixing a precursor
solution for the polymer with a precursor for the nanostructures to
form a mixture; forming nanostructures in the matrix of the polymer
from the precursor of the nanostructures; and forming a polymer
from the precursor solution of the polymer.
[0008] In another non-limiting embodiment of the invention, the
present invention is a method for making a polymer that has
nanostructures incorporated into the matrix of the polymer
comprising: mixing a precursor solution for the polymer comprising
polyvinyl alcohol with a precursor for the nanostructures selected
from monobutyl tin tri-chloride and indium acetate to form a
mixture; forming nanostructures in the matrix of the polymer from
the precursor of the nanostructures: and forming a polymer from the
precursor solution of the polymer.
[0009] In yet another embodiment, the present invention is a method
for making a polymer that has nanostructures incorporated into the
matrix of the polymer comprising: mixing a precursor solution for
poly [bis(diethylene glycol) diallylcarbonate], with a precursor
for the nanostructures comprising titanium iso-propoxide to form a
mixture; forming nanostructures in the matrix of the polymer from
the precursor of the nanostructures; and forming a polymer from the
precursor solution of the polymer.
[0010] In a further embodiment of the invention, the present
invention is a method for making a polymer that has nanostructures
incorporated into the matrix of the polymer comprising: mixing a
precursor solution for trimethylol propane, methylene
bis(4-cyclohexylisocyanate), thiodiethanol with a precursor for the
nanostructures selected from monobutyl tin tri-chloride and indium
acetate to form a mixture; forming nanostructures in the matrix of
the polymer from the precursor of the nanostructures; and forming a
polymer from the precursor solution of the polymer.
DESCRIPTION OF THE INVENTION
[0011] As used herein, all numbers expressing dimensions, physical
characteristics, processing parameters, quantities of ingredients,
reaction conditions, and the like, used in the specification and
claims are to be understood as being modified in all instances by
the term "about". Accordingly, unless indicated to the contrary,
the numerical values set forth in the following specification and
claims may vary depending upon the desired properties sought to be
obtained by the present invention. At the very least, and not as an
attempt to limit the application of the doctrine of equivalents to
the scope of the claims, each numerical value should at least be
construed in light of the number of reported significant digits and
by applying ordinary rounding techniques. Moreover, all ranges
disclosed herein are to be understood to encompass the beginning
and ending range values and any and all subranges subsumed therein.
For example, a stated range of "1 to 10" should be considered to
include any and all subranges between (and inclusive of) the
minimum value of 1 and the maximum value of 10; that is, all
subranges beginning with a minimum value of 1 or more and ending
with a maximum value of 10 or less, e.g., 1.0 to 3.8, 6.6 to 9.7
and 5.5 to 10.
[0012] As used herein, the term "nanostructure" refers to a three
dimensional object wherein the length of the longest dimension
ranges from 1 nm to 1000 nm, for example, from 1 nm to 500 nm, or
from 1 nm to 100 nm, or from 1 to 40 nm.
[0013] As used herein, the phrase "precursor solution for the
polymer" refers to any material that can be used as a starting
material to form the polymer.
[0014] As used herein, the phrase "precursor for the
nanostructures" refers to any material that can be used as a
starting material to form the nanostructures.
[0015] In a non-limiting embodiment, the present invention is a
process for making a polymer having nanostructures incorporated
into the matrix of the polymer. According to the present invention,
the first step in the process involves mixing a precursor solution
for a polymer and a precursor for the nanostructures that are to be
incorporated into the matrix of the polymer to form a mixture. The
precursor solution for the polymer does not include any
nanostructures initially. The exact precursor solution for the
polymer used in the present invention depends on the polymer that
is desired in the end product.
[0016] For example, if the desired end product is a polyvinyl
acetal resin such as polyvinyl butyl (PVB), suitable precursors for
the polymer include, but are not limited to, polyvinyl alcohol
(PVA).
[0017] As another example, if the desired end product is poly
[bis(diethylene glycol) diallylcarbonate], suitable precursors for
the polymer include, but are not limited to, bis(diethylene glycol)
diallylcarbonate monomer.
[0018] As yet another example, if the desired end product is an
aliphatic polyurethane, suitable precursors for the polymer
include, but are not limited to, 1,4-butanediol, trimethylol
propane, and bis(4 isocyanotocyclohexyl) methane which is
commercially available as Desmodur.RTM. W from Bayer Material
Science in Pittsburgh, Pa., and thiodiethanol.
[0019] In a non-limiting embodiment of the invention, a solvent
such as water, ethanol, iso-propanol, butanol, etc. is added to the
mixture.
[0020] According to the present invention, the second step in the
process involves forming the nanostructures from the precursor of
the nanostructures in the matrix of the polymer. The nanostructures
are formed while the viscosity of the polymer is low so that the
nanostructures can incorporate themselves into the matrix of the
polymer. The formation of the nanostructures can be initiated using
various techniques. In a non-limiting embodiment of the invention,
the nanostructures are formed by adjusting the pH of the mixture.
An acid or base, such as ammonia, can be used to adjust the pH of
the solution. Depending on the exact precursor solution of the
polymer and the exact precursor for the nanostructures, there is an
optimum pH range in which the nanostructures will form. One of
ordinary skill in the art will know what the optimum pH range is
based on both precursors.
[0021] In another non-limiting embodiment, the mixture can be
heated to initiate the formation of the nanoparticles. The mixture
can be heated to any temperature provided the mixture is not be
heated to a temperature above that at which the precursor solution
would break down. For example, a precursor solution comprising PVA
cannot be heated above 200.degree. C. because that is the
temperature at which PVA begins to decompose. Similarly to the pH
range, the optimum temperature range at which the particles will
form depends on the exact precursor solution of the polymer and the
exact precursor for the nanostructures. One of ordinary skill in
the art will know what the optimum temperature range is based on
both precursors. Generally, the higher the temperature to which the
mixture is heated and/or the longer the mixture is heated, the
larger the size of the nanostructures that will be formed.
[0022] In yet another non-limiting embodiment of the invention,
forming the nanostructures is accomplished by heating the mixture
after the pH of the mixture is adjusted. In a further non-limiting
embodiment of the invention, forming the nanostructures is
accomplished by heating the mixture and then adjusting the pH of
the mixture.
[0023] In various other non-limiting embodiments of the invention,
the nanostructures can be formed by using one or more of the
following: increasing the pressure on the mixture; by changing the
concentration of the precursor solution for the polymer; by using
an initiator for nanostructure formation; and by seeding (adding no
greater than 5% of the desired nanostructure material based on the
projected weight of the formed nanostructures as is well known in
the art).
[0024] The formed nanostructures are charged species. If the pH of
the solution was adjusted to cause the formation of the
nanostructures, the charge is a result of the pH adjustment. If no
pH adjustment was performed during the nanostructure formation
step, a polymeric stabilizer such as, but not limited to, sodium
polymethacrylate in water and ammonium polymethacrylate in water,
which are both commercially available as Darvan.RTM. 7 and as
Darvan.RTM. C, respectively, from R.T. Vanderbilt Company, Inc. in
Norwalk, Conn. can be added to the solution to create the
charge.
[0025] According to the present invention, the third step involves
forming the polymer from a mixture including the precursor solution
of the polymer. The formation of the polymer can be initiated using
various techniques. One of ordinary skill in the art will know what
technique to use based on the precursor solution of the polymer and
the precursor for the nanostructures.
[0026] In a non-limiting embodiment of the present invention, the
second and third steps described above are switched.
[0027] The method of making polymers having nanostructures
incorporated into the matrix of the polymer according to the
present invention is referred to as "in-situ" process. This means
the nanostructures are formed during the same process that produces
the polymer as opposed to pre-formed nanostructures being dispersed
into a polymer solution.
[0028] During the method of the present invention, ions (cations
and/or anions) can form in the mixture. The formed ions and other
process variables such as the pressure of the system in which the
mixture is held, can affect the final polymer. For example, the
amount of nanostructure formation and the morphology of the
nanostructures will vary depending on the types and amount of ions
present in the solution.
[0029] In the polymer matrix, the nanostructures typically
continually approach one another and collide because they possess
kinetic energy. Under normal circumstances, some of the
nanostructures would become bound together and agglomerate due to
various forces such as Van der Waals forces. As discussed above,
agglomeration is not desirable because the nanostructures can
effectively become regular sized particles and the desired effect
of incorporating the nanostructures is reduced.
[0030] However, the method of the present invention produces
polymers having nanostructures in the matrix of the polymer that do
not agglomerate to the extent the performance of the polymer is
compromised. The nanostructures do not agglomerate because they are
stabilized. The stabilization occurs via three mechanisms: (1)
electrostatic stabilization, (2) steric stabilization and (3) a
combination of electrostatic stabilization and steric
stabilization.
[0031] Because the nanostructures in the polymer matrix are
similarly charged species, they repel each other. This prevents the
nanostructures from coming so close together that they agglomerate.
This phenomenon is referred to as electrostatic stabilization.
[0032] Because the nanostructures are surrounded by polymer
precursor solution when they are formed, the nanostructures lose a
degree of freedom which they would otherwise possess as the
nanostructures approach each other. This loss of freedom is
expressed, in thermodynamic terms, as a reduction in entropy, which
provides the necessary barrier to hinder agglomeration. This
phenomenon is referred to as steric stabilization. The same
principle applies when the method of the invention involves forming
the polymer before forming the nanostructures.
[0033] The polymer formed according to the present invention can
have the following properties. The concentration of the
nanostructures in the polymer matrix can range from 0.1% to 90%,
for example from 3% to 85% or from 15% to 80% based on volume. The
nanostructures in the polymer matrix can have the following shapes:
spherical, polyhedral-like cubic, triangular, pentagonal, diamond
shaped, needle shaped, rod shaped, disc shaped etc. The
nanostructures in the polymer matrix can have an aspect ratio of
1:1 to 1:1,000, for example 1:1 to 1:100.
[0034] The nanostructures in the polymer matrix can have a longest
dimension ranging from 1 nm to 1,000 nm, for example, 1 nm to 500
nm, or 1 nm to 100 nm, or 1 nm to 40 nm. If the nanostructures
agglomerate, the size of the nanostructures could effectively
become so large that the desired performance of the polymer is
compromised. This is the problem with polymers having preformed
nanostructures incorporated into the polymer matrix as discussed
earner.
[0035] The polymers formed according to the present invention can
be used in a number of applications. The formation of specific
polymers having specific nanostructures incorporated into the
polymer matrix is discussed below along with commercial
applications of the polymers.
[0036] In a non-limiting embodiment of the invention, a
polyvinylacetal resin such as polyvinyl butyral (PVB) having indium
tin oxide (ITO) or antimony tin oxide (ATO) nanostructures
incorporated into the polymer matrix is formed. Such a polymer can
be formed in the following manner. In the first step, a precursor
solution for PVB is mixed with a precursor for ITO or ATO
nanostructures.
[0037] An example of a suitable precursor solution for PVB is
polyvinyl alcohol (PVA). Suitable precursors for ITO nanostructures
include monobutyl tin tri chloride and indium acetate. A suitable
precursor for ATO nanostructures is antimony trichloride.
[0038] In the second step, ITO or ATO nanostructures are formed
from the precursor of the nanostructures in the polymer matrix. The
nanostructure formation can be caused by adjusting the pH of the
mixture followed by heating. The pH can be adjusted by introducing
an agent, such as ammonia, into the mixture. For ITO nanostructures
in a PVA aqueous solution, the nanostructures begin to form at a
pH>8. After the pH is adjusted, the mixture is heated to a
temperature of up to 200.degree. C. Heating the solution to a
temperature greater than 200.degree. C. may cause the PVA matrix to
decompose.
[0039] As discussed above, heating the mixture for a longer time
period can increase the size of the nanostructures.
[0040] The --OH groups on the PVA can attach to the nanostructures
so the main chain of the PVA molecule can stabilize the
nanostructures via steric stabilization. By varying the degree of
hydroxylation and the molecular weight of PVA, the stabilization
effect of the PVA can be optimized.
[0041] In the third step, the precursor solution for the polymer is
converted to the polymer. As is well known in the art, the
precursor solution can be converted to PVB by adding PVA solution
to the mixture and then reacting the resulting mixture with
butyraldehyde.
[0042] As discussed above, the properties of the final polymer can
be effected by factors such as the type and amount of ions formed
during the process, the pressure at which the mixture is held,
etc.
[0043] Typically, the final PVB polymer has an average molecular
weight greater than 70,000 as measured by size exclusion
chromatography using low angle laser light scattering. On a weight
basis, the final PVB polymer typically comprises 15 to 25% hydroxyl
groups calculated as polyvinyl alcohol (PVA); 0 to 10% residual
ester groups calculated as polyvinyl ester, and the balance being
acetal groups.
[0044] In a non-limiting embodiment of the invention, the final PVB
polymer is used as an interlayer in a laminated glass transparency
for automotive and architectural applications. As is well known in
the art, a laminated glass transparency can be manufactured by
interposing an interlayer between at least two transparent glass
sheets.
[0045] In this particular embodiment of the invention, a laminated
glass transparency for an automotive and architectural applications
embodiment, it is important that the nanostructures do not
agglomerate. If the nanostructures were to agglomerate and
effectively achieve a diameter of greater than 200 nm, the
nanostructures would scatter visible light rays to such an extent
that transmittance through the interlayer would be insufficient for
the application. A polymer with nanostructures having an acceptable
size for the application, can be determined using a "haze value".
The haze value is associated with the degree to which transparency
is prevented. The larger the nanostructures present in the polymer
matrix, the higher the haze value. According to the present
invention, laminated glass for automotive and
architectural/applications has a haze value of less than or equal
to 1%, for example, less than or equal to 0.3%, or less than 0.2%,
as measured using a Hazeguard System from BYK-Gardner in Columbia,
Md.
[0046] In another non-limiting embodiment of the invention, poly
[bis(diethylene glycol) diallylcarbonate] having oxide
nanostructures such as titania, alumina, zirconia nanostructures
incorporated into the polymer matrix is formed. Such a polymer can
be formed in the following manner. In the first step, a precursor
solution for poly [bis(diethylene glycol) diallylcarbonate] is
mixed with a precursor for titania, alumina, or zirconia
nanostructures.
[0047] Suitable precursor solution for poly [bis(diethylene glycol)
diallylcarbonate] includes, but is not limited to, bis(diethylene
glycol) diallylcarbonate monomer. Suitable precursors for titania
nanostructures include, but are not limited to, titanium
iso-propoxide, titanium (IV) chloride and potassium titanyl
oxalate. Suitable precursors for alumina nanostructures include,
but are not limited to, aluminum iso-propoxide, aluminum
tri-tert-butoxide, aluminum tri-sec-butoxide, aluminum triethoxide,
and aluminum pentanedionate. Suitable precursors for zirconia
nanostructures include, but are not limited to, zirconium
iso-propoxide, zirconium tert-butoxide, zirconium butoxide,
zirconium ethoxide, zirconium 2,4-pentanedionate, and zirconium
trifluoropentane-dionate.
[0048] In the embodiment where a poly [bis(diethylene glycol)
diallylcarbonate] is being formed having titania nanostructures
incorporated into the polymer matrix, the first step can comprise
mixing titanium iso-propoxide with a 1-10 wt % H.sub.2O.sub.2
solution and bis(diethylene glycol) diallylcarbonate monomer. The
H.sub.2O.sub.2 acts as an initiator for titania nanostructures;
particularly, titania nanostructures in the anatase form
Optionally, polymers such as polyoxyethylene (20) sorbitan
monooleate commercially available as Tween.RTM. 80 from ICI Ltd.
(Bridgewater, N.J.) can be added to the solution to help stabilize
the titania nanostructures.
[0049] In the second step, the titania nanostructures are formed
from the precursor by heating the mixture to a temperature of up to
200.degree. C.
[0050] In the third step, the precursor solution for the polymer is
converted into bis(diethylene glycol) diallylcarbonate as is well
known in the art. For example, isopropyl peroxycarbonate (PP) which
is a free radical initiator, can be added to bis(diethylene glycol)
diallylcarbonate monomer. The 1PP can be dissolved directly into
the monomer, poured into a glass mold and heated above 70.degree.
C. for at least 8 hours or more to form poly [bis(diethylene glycol
diallylcarbonate]. The IPP degrades into free radicals that react
with the allyl groups terminating the monomer to begin
polymerization.
[0051] In a non-limiting embodiment of the invention, poly
[bis(diethylene glycol) diallylcarbonate] having titania, alumina,
or zirconia nanostructures incorporated into the matrix of the
polymer can be used as an optical lens. An optical lens made out of
a poly [bis(diethylene glycol) diallylcarbonate] formed according
to the present invention will have a larger elastic modulus and a
higher refractive index than an optical lens made out of standard
poly [bis(diethylene glycol) diallylcarbonate]. As a result of the
higher refractive index, an optical lens made out of polymer formed
according to the present invention does not have to be as thick as
a conventional optical lens to satisfy a severe prescription.
[0052] A polymer with nanostructures having an acceptable size for
the application can be determined using a "haze value". According
to the present invention, an optical lens has a haze value of less
than or equal to 0.5%, for example 0.2%, as measured using a
Hazeguard System from BY K Gardner.
[0053] In a non-limiting embodiment of the invention, a
polyurethane having ITO or ATO nanostructures incorporated into the
polymer matrix is formed. Such a polymer can be formed in the
following manner. In the first step, a precursor solution for the
trimethylol propane, methylene bis(4-cyclohexylisocyanate)
thiodiethanol is mixed with a precursor for ITO or ATO
nanostructures.
[0054] A suitable precursor solution for the polyurethane is
trimethylol propane, methylene bis(4-cyclohexylisocyanate),
thiodiethanol includes, but is not limited to, 1,4-butanediol.
Suitable precursors for ITO nanostructures include monobutyl tin
tri chloride and indium acetate. A suitable precursor for ATO
nanostructures is antimony tri-chloride.
[0055] In the second step, ITO or ATO nanostructures are formed
from the precursor. The nanostructure formation can be caused by
adjusting the pH of the solution by introducing an agent, such as
ammonia, into the mixture followed by heating the mixture. For ITO
nanostructures, the ITO nanostructures start to form at pH 8. After
the pH is adjusted, the mixture is heated to a temperature of up to
200.degree. C. As discussed above, heating the mixture for a longer
time period can increase the size of the nanostructures.
[0056] In the third step, the 1,4-butanediol is mixed into
trimethylol propane, methylene bis(4-cyclohexylisocyanate),
thiodiethanol as is well known in the art. For example, 1,4
butanediol, thiodiethanol, trimethylol propane (TMP), and
Desmodur.RTM. W can all be mixed into a vessel and heated to
180.degree. F. The mixture is mixed under vacuum for approximately
15 minutes, and then a fin catalyst, such as dibutyltindilaurate or
bismuth carboxylate, is added to the mixture in a 25 ppm
concentration. The mixture is then cast into a glass mold and cured
for at least 20 hours at 250.degree. F. to form the
polyurethane.
[0057] In a non-limiting embodiment, trimethylol propane, methylene
bis(4-cyclohexylisocyanate), thiodiethanol having ITO or ATO
nanostructures incorporated into the polymer matrix is used to form
an anti-static coating for aircraft windows. The polymer with the
nanostructures has an elastic modulus that is greater than that of
the standard trimethylol propane, methylene
bis(4-cyclohexylisocyanate) thiodiethanol without ITO/ATO
nanoparticles.
[0058] A polymer with nanostructures having an acceptable size for
the aircraft window application can be determined using a "haze
value". According to the present invention, a laminated aircraft
window has a haze value of less than or equal to 1%, for example
0.5%, as measured using a Hazeguard System from BYK Gardner.
[0059] It will be readily appreciated by those skilled in the art
that modifications may be made to the invention without departing
from the concepts disclosed in the foregoing description. Such
modifications are to be considered as included within the scope of
the invention. Accordingly, the particular embodiments described in
detail hereinabove are illustrative only and are not limiting as to
the scope of the invention, which is to be given the full breadth
of the appended claims and any and all equivalents thereof.
* * * * *