U.S. patent application number 13/935650 was filed with the patent office on 2013-11-07 for latent hardener with improved barrier properties and compatibility.
The applicant listed for this patent is Trillion Science, Inc.. Invention is credited to Jing Liang, Rong-Chang Liang, John J. McNamara, Yurong Ying.
Application Number | 20130295381 13/935650 |
Document ID | / |
Family ID | 44558876 |
Filed Date | 2013-11-07 |
United States Patent
Application |
20130295381 |
Kind Code |
A1 |
Ying; Yurong ; et
al. |
November 7, 2013 |
LATENT HARDENER WITH IMPROVED BARRIER PROPERTIES AND
COMPATIBILITY
Abstract
A curing agent for epoxy resins that is comprised of the
reaction product of an amine, an epoxy resin, and an
elastomer-epoxy adduct; compositions containing the curing agent
and an epoxy resin; the compositions are useful in electronic
displays, circuit boards, semi conductor devices, flip chips and
other applications.
Inventors: |
Ying; Yurong; (Fremont,
CA) ; McNamara; John J.; (El Sobrante, CA) ;
Liang; Jing; (Walnut Creek, CA) ; Liang;
Rong-Chang; (Cupertino, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Trillion Science, Inc. |
Fremont |
CA |
US |
|
|
Family ID: |
44558876 |
Appl. No.: |
13/935650 |
Filed: |
July 5, 2013 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13236915 |
Sep 20, 2011 |
8481612 |
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13935650 |
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12762892 |
Apr 19, 2010 |
8067484 |
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13236915 |
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61313199 |
Mar 12, 2010 |
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Current U.S.
Class: |
428/354 ;
523/428; 525/526 |
Current CPC
Class: |
C09J 163/00 20130101;
C08L 63/00 20130101; C09J 9/02 20130101; C08G 18/7664 20130101;
C09D 163/00 20130101; Y10T 428/24802 20150115; C08G 18/58 20130101;
C08G 59/186 20130101; Y10T 428/31515 20150401; H05K 3/321 20130101;
C08G 59/4261 20130101; C08J 2363/00 20130101; C08G 18/758 20130101;
Y10T 428/31511 20150401; C08G 59/50 20130101; Y10T 428/2848
20150115; C08J 3/241 20130101; H05K 3/303 20130101 |
Class at
Publication: |
428/354 ;
525/526; 523/428 |
International
Class: |
C09J 163/00 20060101
C09J163/00; C09D 163/00 20060101 C09D163/00; C08L 63/00 20060101
C08L063/00 |
Claims
1.-9. (canceled)
10. A composition comprising an epoxy resin and a curing agent that
is comprised of the reaction product of: (a) an amine, and (b) an
epoxy resin, and (c) an elastomer-epoxy adduct.
11. The composition of claim 10 wherein the curing agent is the
reaction product of: (a) an amine, and (b) an epoxy resin, and (c)
a carboxyl-terminated butadiene-acrylonitrile (CTBN)-epoxy adduct;
wherein the elastomer-epoxy adduct is a carboxyl-terminated
butadiene-acrylonitrile (CTBN)-epoxy adduct which functions as a
dispersant; wherein the amine and the epoxy resin are reacted in
the presence of the dispersant to produce a dispersion of epoxy
resin particles; wherein the particles are encapsulated in a
polymer shell.
12. The composition of claim 11 wherein the nitrile content of the
CTBN is about 12-35% by weight.
13. The composition of claim 12 wherein the wherein the nitrile
content is about 20-33% by weight.
14. The composition of claim 10 wherein the composition is
formulated such that it is functional as an adhesive, a conducting
adhesive, a composite, a molding compound, an anisotropic
conducting film (ACF) adhesive, a non-random array ACF, a
non-conductive adhesive film (NCF), a coating, an encapsulant, an
underfill material, or as a lead free solder.
15. An electronic display comprising an electronic component
affixed to a substrate by an epoxy adhesive wherein the epoxy
adhesive incorporates the curing agent of claim 1.
16. A circuit board comprising an electronic component affixed to a
board substrate with an epoxy adhesive, the epoxy adhesive
incorporating the curing agent of claim 1.
17. A flip chip comprising an integrated circuit chip mounted to a
substrate with an epoxy adhesive, wherein the epoxy adhesive
comprises the curing agent of claim 1.
18. A semiconductor device comprising an electronic component
affixed to a substrate with an epoxy adhesive wherein the epoxy
adhesive includes the curing agent of claim 1.
19. The composition of claim 10 wherein the composition is a 1-part
adhesive composition.
20. The composition of claim 19 wherein the composition shows
adhesion after cure at interfaces, low shrinkage on cure, and low
coefficient of thermal expansion (CTE).
21. The composition of claim 19 wherein the composition is
formulated such that it is useful as a matrix for a composite
material or molding compound.
22. A fixed array ACF comprising gold particles dispersed in the
adhesive film in a predetermined pattern, the adhesive film
comprising an epoxy adhesive and a curing agent wherein the curing
agent is the reaction product of an amine, an epoxy resin, and an
elastomer-epoxy adduct.
23. The composition of claim 10 wherein the composition is
formulated such that it is useful as a High Tg 1-part molding
compound comprising a protected phenolic compound, where the
protected phenolic compound comprises an aryl glycidyl carbonate
moiety.
24. The composition of claim 23 wherein the composition is
formulated such that it is useful as a sheet molding compound
(SMC), a bulk molding compound (BMC), or a dough molding compound
(DMC).
Description
CROSS REFERENCE TO RELATED APPLICATION
[0001] This application claims the benefit of U.S. Provisional
Application Ser. No. 61/313,199 filed Mar. 12, 2010, the contents
of which are hereby incorporated by reference.
FIELD OF THE INVENTION
[0002] This invention relates to latent hardeners for epoxy resins
and, more particularly, to latent hardeners comprised of a core
material that is encapsulated or coated in a step-wise manner with
two or more shell materials.
BACKGROUND OF THE INVENTION
[0003] Epoxy adhesives have been known for over 50 years and were
one of the first high temperature adhesives to become
commercialized. Once cured, the material retains its adhesive
properties over a large range of temperatures, has high shear
strengths, and is resistant to weathering, oil, solvents, and
moisture. The adhesive is available commercially as either a 1-part
adhesive or 2-part adhesive and is available in several forms, such
as pastes, solvent solutions, and supported films. Of the three
forms, the 1-part adhesive film generally provides good adhesive
strength with better thickness uniformity and has found practical
use in the development of anisotropic conducting films for
electronics, most notably flat panel displays.
[0004] To construct a 1-part adhesive film, one typically combines
all at once, a latent hardener, multi-functional epoxy resins,
phenoxy resins, additives, and optionally fillers. This composition
is then cast as a film on a release layer. During the bonding
process, the adhesive is transferred to one particular surface and
the release layer removed. Another surface is brought into contact
with the film, and the adhesive hardened or cured into a strong
thermosetting adhesive through the application of heat and/or
pressure. In this example, the two components of the adhesive that
enable the material to cure into a thermoset adhesive are the
hardener and the multi-functional epoxy. It is the later, that sets
up the cross-linked network, but it is the former that enables this
to happen. During the curing process, the latent hardener initiates
the polymerization of the multi-functional epoxy by first forming
ring-opened adducts with the oxiranes of the epoxy resin. Once
produced, the addition products cause a cascade of ring-opened
species that propagate through the adhesive, finally producing a
cross-linked thermoset material.
[0005] The active ingredient of the hardener is usually comprised
of the reaction product of an amine compound, like an imidazole,
and an epoxy resin. Such adducts are known to initiate and
accelerate the cure of epoxy resins (Heise, M. S.; Martin, G. C.
Macromolecules, 1989, 22 99-104; Heise, M. S.; Martin, G. C. J.
Poly. Sci.: Part C: Polym. Lett. 1988, 26, 153-157; Barton, J. M;
Shepherd, P. M.; Die Makromolekular Chemie 1975 176, 919-930). One
drawback of these however is that they are so effective as
curatives they cannot be used directly into a 1-part adhesive
because once added, they would start to kick-off the cure in a
relative short period of time. What one would see therefore is a
slow increase in the viscosity of the composition, while one is
attempting to make the adhesive and its film, as the hardener
continues to accelerate the ring-opening polymerization of the
epoxy moieties. This phenomenon is most commonly referred to as
reduced workable lifetime, in other words, the time available to
assemble the adhesive and make the film was dramatically reduced
because of premature hardening. Therefore, to stop this from
happening, one usually does not use amine-epoxy adducts themselves
as hardeners, but instead what is typically done is to encapsulate
or coat the amine-epoxy adduct with a protective shell of material
that sequesters the amine-epoxy adduct from the adhesive
environment. Once incorporated into the adhesive, the amine-epoxy
adduct is released from its protective shell through the
application of heat and/or pressure. Such latent hardeners
described here are commonly called to as a core-shell latent
hardener, where the core in this case is an amine-epoxy adduct and
the shell is the protective shell.
[0006] There is one significant trade-off often encountered with
core-shell latent hardeners, which is the cure speed is often
slowed and the cure temperature often increased because of the
inclusion of a protective shell, which must be broken or rendered
permeable in order to allow the core material to be released into
the adhesive environment or matrix. Without being bound by any
particular theory, it is well known that as one increases the
barrier properties of the shell material using such means, like
increasing the thickness of the shell, cross-linking density, or
T.sub.g of the shell, or by increasing the degree of
incompatibility between the shell and the core material or the
adhesive matrix, it takes more energy to release the amine-epoxy
adduct into the adhesive environment. What one has therefore is a
hardener that when formulated into a 1-part adhesive has the
desired property of increased shelf life stability, but at the
expense of a lower curing temperature and a reduction of cure
speed. Therefore, it continues to be a constant balance to prepare
a core-shell latent hardener that has just enough of a protective
shell to protect the core material at normal storage conditions,
but not too much as to slow down the cure speed of the adhesive.
Also, the release of the core material may be triggered at a
reasonably low temperature and completed within a narrow
temperature range.
[0007] One of the most frequently used core-shell latent hardeners
are those comprised of core-shell materials, as described in U.S.
Pat. No. 4,833,226, U.S. Pat. No. 5,219,956, US 2006/0128835, US
2007/0010636, US 2007/0055039, US 2007/0244268, EP 1,557,438, EP
1,731,545, EP 1,852, 452, and EP 1,980,580. The hardeners described
here are obtained, first by the synthesis of a lump of core
material, which is then pulverized into micro-sized particles that
are irregular in shape. The core material is the reaction product
of an amine compound and an epoxy resin and said core material
functions as a hardener for epoxy compositions, such as that found
in adhesives and coatings. To improve the storage stability of the
core material and prevent premature curing, it is encapsulated with
a shell of a material that is impervious to components of the epoxy
composition, such as solvent, diluent, low molecular weight
epoxides and additives. To accomplish this, the pulverized solid is
added to a mixture of polyfunctional isocyanate, an active hydrogen
compound, like water, and an epoxy resin. The chemistry of said
encapsulation procedure relies on the cross-linking reactions
and/or hydrolysis of the polyisocyanate compound to form a
cross-linked shell coating around the particles. Typical
cross-linking structures of the shell include, but are not limited
to, urea, urethane, carbamate, biuret, allophanate, etc. However,
the crosslinking reactions take places randomly without
discrimination in the continuous phase and at the interface. It is
highly likely that some core particles are not fully encapsulated,
while unwanted byproducts such as crosslinked polyurea particles
are produced in the continuous phase. Moreover, the core particles
prepared by this process are of irregular shape with a very broad
distribution of shape and particle size, the uniformity of the
thickness and crosslinking density of the shell formed thereon is
very poor. As a result, the encapsulated hardener particles
typically show a very broad distribution of release property and
the 1-part adhesive formulated with this type of hardener capsules
often shows poor shelf-life stability and a sluggish curing profile
or a high curing temperature.
[0008] There is another group of inventions, namely EP 459,745, EP
552,976, U.S. Pat. No. 5,357,008, U.S. Pat. No. 5,480,957, U.S.
Pat. No. 5,548,058, U.S. Pat. Nos. 5,554,714, 5,561,204, U.S. Pat.
No. 5,567,792, and U.S. Pat. No. 5,591,814, that also describe core
shell latent hardeners, which unlike those above are spherical in
shape. The core material is obtained as a spherical particle and is
synthesized from the reaction of an amine with an active hydrogen
atom (e.g., imidazole) and an epoxy resin, in an organic medium and
in the presence of a dispersant. The amine, epoxy resin, and
dispersant are soluble in the organic medium, while the reaction
product, the core material, is not, and as a result the core
particle precipitates out from solution as a stable dispersion with
a relatively narrow size distribution. The most important factor to
make a stable dispersion of desirable particle size with a narrow
size distribution is the nature of the dispersant and the inventors
show examples that use dispersants from the class of graft of
polyacrylates, polyacrylamides, polyvinyl acetates, polyethylene
oxides, polystyrenes, and polyvinyl chlorides. Once isolated, the
spherical core material is encapsulated with an isocyanate to
prepare a spherical core-shell latent hardener.
[0009] One disadvantage of the aforementioned latent hardeners is
the need of the shell material to be free of defects, such as such
as holes, voids, thin areas, or areas comprised of insufficient
cross-link density. These defects would enable the core to escape
from the protective shell prematurely, either during processing or
storage of the finished article. Either way, this premature release
of core from the encapsulated latent hardener would show up as a
loss of storage stability and shelf-life (in the case of a 1-part
epoxy adhesive). This deficiency; however, can be overcome by the
application of additional and successive layers of the shell
material over the preexisting shell, thus filling in and coating
the defects with an additional layers shell material.
[0010] Another limitation of the prior art is that in an attempt to
make the protective shell more impervious and thereby improving its
barrier properties, the compatibility of the shell with the
surrounding epoxy composition was neglected. The prior art teaches
encapsulation in the presence of an isocyanate, and optionally
water and additional epoxy. What one then obtains is a shell
comprised of a cross-linked polyurethane and optionally a polyurea.
When formulated into an epoxy adhesive, the now hard and highly
cross-linked shell could have poor capability with the surrounding
epoxy. An example of this would be a mismatch of surface tensions
between the surface of the shell and the epoxy; which would show up
as a dewetting phenomenon in which the epoxy fails to adequately
wet and spread over the surface of the shell material. As a
consequence therefore one would see that after curing, the adhesive
would contain voids and regions of inhomogeneous curing, both of
which would lead to a reduction of adhesive strength.
[0011] There remains a need for core-shell latent hardeners with
improved barrier properties to prevent premature cure.
Additionally, there is a need of encapsulated latent hardeners with
improved epoxy compatibility.
SUMMARY OF THE INVENTION
[0012] This invention relates to latent hardeners or catalysts for
thermosets such as epoxy resins and, more particularly, to latent
hardeners or catalysts comprised of a core material that is
encapsulated or coated with two or more shell materials. The core
material, which is a curative for epoxy resins, is further
comprised of the reaction product of an amine (e.g., imidazoles,
piperazines, primary aliphatic amines, and secondary aliphatic
amines) and an epoxy resin. In one embodiment, the core material is
synthesized in an organic medium and in the presence of a
dispersant which is the reaction product of carboxyl terminated
poly(butadiene-co-acrylonitrile) (CTBN) and an epoxy resin. In one
embodiment, the reaction product of a CTBN and an epoxy resin is
capable of providing a stable dispersion of spherical-shaped core
particles with a narrow size distribution. In another embodiment
near 100% conversion is obtained by using a slight excess of epoxy.
In another embodiment, the spherical-shaped core particles are
encapsulated by reacting with a multi-functional isocyanate or
thioisocyanate. Optionally, an epoxy resin is added at the same
time as the isocyanate to build up the thickness of the
encapsulated shell. In still another embodiment, once formed, the
core material is fully encapsulated with two or more shell
materials that are applied in a step-wise manner using a
multi-functional isocyanate, or a mixture of isocyanate and
multi-functional epoxy resin, or a mixture of an isocyanate and
epoxy compatible material, such as CTBN or polyacrylate modified
epoxy, or a mixture of an isocyanate, multi-functional epoxy, and
an epoxy compatible material. Curable compositions prepared using
the particles have excellent storage stability and improved curing
properties.
[0013] One aspect of this disclosure relates to an improvement to
the barrier properties and solvent resistance of a latent hardener
or catalyst.
[0014] Another aspect of this disclosure relates to an improvement
of barrier properties and solvent resistance of a latent hardener
or catalyst.
[0015] Another aspect of this disclosure relates to an improvement
of compatibility of the latent hardener or catalyst with an epoxy
resin or composition.
[0016] Another aspect of this disclosure relates to a latent
hardener or catalyst of a spherical-shape and which is fully
encapsulated.
[0017] Another aspect of this disclosure relates to a latent
hardener or catalyst that releases the core material at the desired
temperature, pressure, or combination of both.
[0018] Another aspect of this disclosure relates to a latent
core-shell latent hardener or catalyst, wherein the hardener or
catalyst is comprised of a stable dispersion of spherical-shaped
particles.
[0019] Another aspect of this disclosure relates to a process of
making spherical-shaped core particles using a dispersant, wherein
said dispersant is the reaction product (adduct) of a
carboxyl-terminated butadiene-acrylonitrile rubber (CTBN) and an
epoxy resin.
[0020] Another aspect of this disclosure relates to a curing agent
comprised of an amine compound, an epoxy resin, and a dispersant,
wherein said dispersant is the adduct of CTBN and an epoxy
resin.
[0021] Another aspect of this disclosure relates to a process for
making the curing agent.
[0022] Another aspect of this disclosure relates to a masterbatch
that is comprised of the curing agent.
[0023] Another aspect of this disclosure relates to an electronic
device or a flat panel display comprising the composition that is
comprised of the curing agent disclosed herein. For example a
common method that is used to connect the driver integrated circuit
(IC) to the electronic device or flat panel display is through the
use of either a chip-on-glass (COG) or chip-on-film (COF). In the
constructions of the COG and COF, anisotropic conducing film
adhesives (ACF) and non-conducting film adhesives (NCF) are
typically used to attach the COG or COF to the driver IC and it is
the curing agent that enables the adhesives to cure and produce a
permanent bond between the components. Accordingly, in one
embodiment, the integrated circuit chip or other electronic
component is attached using an epoxy adhesive containing the curing
agent described herein.
[0024] Another aspect of this disclosure relates to a composition
containing the curing agent, where the composition is an adhesive,
conducting adhesive, composite, molding compound, anisotropic
conducting film (ACF) adhesive, non-random array ACF,
non-conductive adhesive film (NCF), coating, encapsulant, underfill
material, lead or free solder.
[0025] Another aspect of this disclosure relates to a circuit board
comprising an epoxy adhesive composition comprised of the curing
agent that is disclosed herein. Traditionally, the electronic
components, such as resistor, capacitor, and IC are assembled to
the circuit board through a soldering process. This process
requires high temperature and generates waste. However, an ACF, NCF
or conductive adhesive containing the disclosed curing agent
provides an alternative method to mount the electronic components
on the circuit board without the use to high temperatures, waste,
and toxic heavy metals. In this application, ACF and NCF provide
the electrical contact and secure the component to the board.
[0026] Another aspect of this disclosure relates to an electronic
device or display which is assembled using an epoxy adhesive
composition that contains the curing agent disclosed herein.
[0027] Another aspect of this disclosure relates to a flip chip
comprising the adhesive composition containing the curing agent
disclosed herein. Traditionally a flip chip is a chip that mounted
to the substrate in two steps. First, the chip is bonded to the
substrate through soldering or eutectic bonding. Underfill
material, typically in liquid form, is then filled in the gap and
cured between the chip and the substrate. Replacing the soldering
or eutectic bonding process with an ACF or NCF containing the
disclosed curing agent is an alternative method to accomplish the
first step. Not only does the adhesive approach provided advantages
encountered with circuit boards, but the ACF and NCF also function
as the underfill material to fill the gap between the chip and the
substrate thereby accomplishing the process in a single step, where
two were used before.
[0028] Another aspect of this disclosure relates to an electronic
device or display where the composition is cured, partially cured,
or un-cured and is comprised of the curing agent.
[0029] Another aspect of this disclosure relates to a semiconductor
device, such as a high definition LCD, Electronic Paper (ePaper),
mini projectors, and cell phones that are comprised of flat panel
displays, electronic devices, circuit boards, and flip chips in
which an epoxy adhesive containing the curing agent disclosed
herein is used as described above.
[0030] Another aspect of this disclosure is a fixed array ACF,
where the fixed array ACF is an ACF wherein the gold particles are
dispersed in the adhesive film in a predetermined pattern, such as
that described in Trillion's patent application 2006/0280912 A1
wherein an epoxy adhesive containing the curing agent disclosed
herein is used to construct the array.
[0031] Another aspect of this disclosure is a High T.sub.g 1-part
molding compound comprising a protected phenolic compound as
described in U.S. application Ser. No. 12/008,375 filed Jan. 10,
2008 which is herein incorporated by reference, where the protected
phenolic compound comprises an aryl glycidyl carbonate moiety, and
the curing agent disclosed herein.
[0032] Still another aspect of this disclosure are 1-part
composites, including prepreg composites and molding compounds,
such as sheet molding compounds (SMC), bulk molding compounds
(BMC), and dough molding compounds (DMC) wherein the curing agent
is the curing agent disclosed herein.
[0033] Still another aspect of the disclosure is adhesives and
coating applications, including solder mask and impregnation
coatings in which the curing agent is the curing agent disclosed
herein.
[0034] Another aspect of this disclosure employs epoxy resins
containing the curing agent disclosed herein in assembly and
packaging for semi-conductor applications such as described in
Colclaser, Roy A.; "Microelectronics Processing and Device Design";
John Wiley & Sons, Publishers: New York, 1980; Chapter 8, page
pp. 163-181.
[0035] Another aspect of this disclosure relates to the circuit
board where the composition is cured, partially cured, or un-cured
and is comprised of the curing agent disclosed herein.
[0036] Another aspect of this disclosure relates to a flip chip
where the epoxy adhesive composition described herein is cured,
partially cured, or un-cured and is comprised of the curing
agent.
[0037] Another aspect of this disclosure relates to a semiconductor
device comprising the composition containing the curing agent.
Another aspect of this disclosure relates to a semiconductor device
where the composition is cured, partially cured, or un-cured and is
comprised of the curing agent.
[0038] Another aspect of this disclosure relates to a composition,
where the composition is a 1-part adhesive composition having a
substantially long shelf-life at storage conditions and the
composition is reactive at either the curing temperature or the
molding temperature, and the composition contains the curing agent
disclosed herein.
[0039] Another aspect of this disclosure relates to a composition
containing the curing agent, where after cure the composition shows
adhesion at interfaces, low shrinkage on cure, and low coefficient
of thermal expansion (CTE).
[0040] Another aspect of this disclosure relates to a composition
containing the curing agent, where the composition is a matrix for
a composite material or molding compound.
BRIEF DESCRIPTION OF THE DRAWINGS
[0041] FIG. 1 is a drawing showing a core material encapsulated
with two protective shell materials. In the case for improved
latent hardener compatibility the composition of protective shell 2
is selected such that is comprised of an epoxy compatible material,
while the composition of shell 1 is selected based only on its
barrier properties.
[0042] FIG. 2 is an electron micrograph of core particles of
spherical shape comprised of 2-methylimidazole, diglycidyl ether of
bisphenol A (DGEBA), and the CTBN-epoxy adduct isolated from CVC
Thermoset Materials HyPox.TM. RK84.
[0043] FIG. 3 is an electron micrograph of core particles of
spherical shape comprised of 2-methylimidazole, diglycidyl ether of
bisphenol A (DGEBA), and the CTBN-epoxy adduct isolated from CVC
Thermoset Materials HyPox.TM. RK84, wherein the core particle is
encapsulated with 4,4'-methylenebis(phenyl isocyanate) (MDI).
[0044] FIG. 4 is an electron micrograph of a single core particle
of spherical shape comprised of 2-methylimidazole, diglycidyl ether
of bisphenol A (DGEBA), and the CTBN-epoxy adduct isolated from CVC
Thermoset Materials HyPox.TM. RK84.
[0045] FIG. 5 is the chemical structure of a CTBN-epoxy adduct (c)
where a hydroxyl-functional epoxy resin (b) such as that of CVC
Thermoset Specialties HyPox RK84 is used in the synthesis along
with CTBN (a). The residual unreacted epoxy resin (b) is removed
prior to (c) being used as a dispersant.
[0046] FIG. 6 is the chemical structure of a CTBN-epoxy adduct (e)
where disglydicyl ether of bisphenol A (d) such as that of CVC
Thermoset Specialties HyPox RA1340 is used in the synthesis, along
with CTBN (a).
DETAILED DESCRIPTION OF THE INVENTION
[0047] In accordance with one embodiment, the curing agent is an
adduct of: (i) an amine, (ii) an epoxy compound, and (iii) an
adduct of an elastomer and an epoxy resin. The elastomer/epoxy
resin adduct functions as an reactive dispersant enabling the
formation of a dispersion of spherical un-encapsulated particles in
the reaction medium.
[0048] Another aspect of the invention is a method for the
preparation of fine spherical core particles of a curing agent that
comprises reacting an amine compound with an epoxy/elastomer adduct
followed by an epoxy compound, in the presence of a continuous
phase at elevated temperatures with agitation, and recovering fine
spherical particles formed from the reaction mixture solution.
Optionally, the recovered particles may be filtered to remove
aggregated particles and classified by methods such as gravity
fractionation, filtration, sedimentation, field flow fractionation,
and field flow classification to remove small satellite particles.
The continuous phase is an organic solvent or solvent mixture
comprised of either a solvent capable of dissolving the amine
compound, the epoxy compound and the epoxy/elastomer adduct but
incapable of dissolving the adduct formed from the three reactants
or a mixture of a solvent and non-solvent, where the solvent is
capable of dissolving the amine compound, the epoxy compound and
the epoxy/elastomer adduct but incapable of dissolving the adduct
particles formed from the three reactants or a mixture and the
non-solvent is a non-solvent for the amine compound, the epoxy
compound, the epoxy/elastomer adduct, and the adduct particles
formed from the three reactants. The selection of the continuous
phase affects the dispersion stability and the particle size and
particle size distribution.
[0049] Yet another embodiment of the invention is a heat curable
composition that comprises, as its major components, an epoxy
composition and spherical particles of the curing agent. In this
case, the spherical particles of the curing agent of this invention
are not soluble or swellable in the epoxy composition. In one
embodiment the particles have a melting flow temperature of at
least about 50.degree. C. and a particle diameter of 0.1 .mu.m to
30 .mu.m. The particles are incorporated in the adhesive in an
amount of about 1 to 60 parts by weight per 100 parts by weight of
the epoxy resin.
[0050] The present invention also includes a curing agent
masterbatch for epoxy resins wherein the masterbatch comprises a
liquid epoxy resin in which fine spherical particles of the curing
agent are uniformly dispersed. In a particular embodiment, the
particles have been reacted with 1 to 100 parts by weight of a
polyfunctional isocyanate compound, and optionally with 1-100 parts
by weight of an epoxy compound, based on 100 parts by weight of
said particles. The particles are then allowed to react one or more
additional times in successive steps with 1 to 100 parts by weight
of a polyfunctional isocyanate compound, and optionally with 1-100
parts by weight of a multifunctional epoxy compound, and optionally
with 1-100 parts by weight of an epoxy compatible material, based
on 100 parts by weight of said particles.
[0051] The present invention further includes a method for
preparation of a curing agent masterbatch for epoxy resin with
comprises the step of dispersing spherical particles of the curing
agent in an epoxy resin at a temperature below the melt flow
temperature of said spherical particles.
[0052] Curing Agent Epoxy Plus Amine Compound
[0053] In the present invention the amine compounds and the epoxy
compounds which can be employed in the preparation of the curing
agent are selected based on its chemical structure which promotes
the curing reaction by anionic polymerization, its melting point,
and its compatibility with the epoxy resin which will be cured in a
molten or plasticized viscoelastic state, its quick curability and
its reactivity. The melting flow temperature is defined herein as
the temperature at which the substance begins to flow as a molten
fluid, as determined by the conventional methods. Examples of amine
and epoxy compounds useful in certain embodiments of the invention
are disclosed in EP 459,745, EP 552,976, U.S. Pat. No. 5,357,008,
U.S. Pat. No. 5,480,957, U.S. Pat. No. 5,548,058, U.S. Pat. Nos.
5,554,714, 5,561,204, U.S. Pat. No. 5,567,792, and U.S. Pat. No.
5,591,814, which are incorporated herein by reference.
[0054] Amine Compound
[0055] While any amine compound can be used, the selection of the
amine will be based upon the nature of the epoxy compound. An amine
is selected that reacts with the epoxy compound but enables the
reaction without full polymerization. While it is possible to use
substantially any amine compounds when reacting monofunctional
epoxy compounds, when reacting polyfunctional epoxy compounds, an
amine compound which has only one active hydrogen, i.e., a
secondary amino group that contributes to the reaction of the epoxy
group. Use of compounds having a tertiary amino group, i.e., having
no active hydrogen, is also permitted. The following compounds are
illustrative examples of amine compounds which can be combined with
bifunctional bisphenol A diglycidyl ether: imidazoles represented
by 2-methylimidazole and 2,4-dimethylimidazole, piperazines
represented by N-methyl piperazine and N-hydroxylethyl-piperazine,
anabasines represented by anabasine, pyrazoles represented by
3,5-dimethyl-pyrazole, purines represented by
tetra-methyl-quanidine or purine, pyrazoles represented by
pyrazole, and triazoles represented by 1,2,3-triazole, and the
like.
[0056] Epoxy Compound
[0057] Examples of epoxy compounds are monofunctional epoxy
compounds such as n-butyl glycidyl ether, styrene oxide and
phenylglycidyl ether; bifunctional epoxy compounds such as
bisphenol A diglycidyl ether, bisphenol F diglycidyl ether,
bisphenol S diglycidyl ether and diglycidyl phthalate;
trifunctional compounds such as triglycidyl isocyanurate,
triglycidyl p-aminophenol; tetrafunctional compounds such as
tetraglycidyl m-xylene diamine and
tetraglycidyldiaminodiphenylmethane; and compounds having more
functional groups such as cresol novolac polyglycidyl ether, phenol
novolac polyglycidyl ether and so on. The selection of epoxy is
also determined by the type of the amine compound to be combined.
The epoxy compounds are also selected based upon the softening
point of the adduct formed and the compatibility in a molten state
with respect to the epoxy resin which is to be cured. Since the
majority of the epoxy resins to be cured comprise bisphenol A
diglycidyl ether, this compound is most typically used as the
starting material for the preparation of an adduct. In one
embodiment, epoxy compounds having an epoxy equivalent weight of,
at most about 1,000, and preferably at most about 500 are typically
employed.
[0058] Solvent
[0059] It is also important to select a solvent system which can
dissolve the amine compounds and the epoxy compound as the starting
materials but can precipitate the adduct in the form of particles
without dissolution. Examples of solvents that can be used in
certain embodiments of the present invention are methyl isobutyl
ketone, methyl isopropyl ketone, methyl ethyl ketone, acetone,
n-butylacetate, isobutyl acetate, ethyl acetate, methyl acetate,
tetrahydrofuran, 1,4-dioxane, cellosolve, ethyleneglycol monoethyl
ether, diethyleneglycol dimethyl ether, anisole, toluene, p-xylene,
benzene, methylene chloride, chloroform, trichloroethylene,
chlorobenzene and pyridine. These solvents can be used alone, or
two or more solvents can be used together.
[0060] Non-Solvent
[0061] Additionally a non-solvent may need to be added to assist
with forcing the amine compound to react with the epoxy
functionalities of the dispersion stabilizer and epoxy resin. A
non-solvent in the case is any solvent that does not dissolve
either the amine compound, dispersion stabilizer, or epoxy resin.
One possible class of compounds that can be used as non-solvents
are linear or branched aliphatic compounds such as heptane, hexane,
octane, iso-octane, petroleum ether, and the like. One example of a
non-solvent in combination with a solvent is a mixture of heptane
and MIBK. In addition to the above-mentioned solvent and
non-solvent, a diluent or a weak solvent may be optionally used to
widen the formulation or process window.
[0062] Dispersion Stabilizer or Dispersant
[0063] The dispersion stabilizer or dispersant enables a stable
dispersion of the adduct particles in the reaction medium. Without
such a dispersion stabilizer, the particles of the adduct formed
may aggregate and precipitate out as a viscous mass during the
reaction, and thus the desired fine spherical particles cannot be
obtained. An optimum dispersant is important for the preparation of
a stable dispersion with a narrow particle size distribution.
Reactive dispersants are often more effective than non-reactive
dispersants since desorption or migration of the dispersant away
from the particle surface is less likely once it reacts with the
particle phase. Elastomer/epoxy adducts are used as reactive
dispersants in accordance to this invention. A suitable molecular
weight range of the reactive dispersant is from about 1,000 to
300,000, preferably from about 2,000 to 100,000, and most
preferably from about 3,000 to 10,000.
[0064] Epoxy/Elastomer Adducts as Reactive Dispersants
[0065] The epoxy/elastomer adduct itself generally includes about
1:5 to 5:1 parts of epoxy or other polymer to elastomer, and more
preferably about 1:3 to 3:1 parts of epoxy to elastomer. More
typically, the adduct includes at least about 5%, more typically at
least about 12% and even more typically at least about 18%
elastomer and also typically includes not greater than about 50%,
even more typically no greater than about 40% and still more
typically no greater than about 35% elastomer, although higher or
lower percentages are possible. The elastomer suitable for the
adduct may be functionalized at either the main chain or the side
chain. Suitable functional groups include, but are not limited to,
--COOH, --NH.sub.2'--NH--, --OH, --SH, --CONH.sub.2, --CONH--,
--NHCONH--, --NCO, --NCS, and oxirane or glycidyl group, etc. The
elastomer optionally may be vulcanize-able or post-crosslink-able.
Exemplary elastomers include, without limitation, natural rubber,
styrene-butadiene rubber, polyisoprene, polyisobutylene,
polybutadiene, isoprene-butadiene copolymer, neoprene, nitrile
rubber, butadiene-acrylonitrile copolymer, butyl rubber,
polysulfide elastomer, acrylic elastomer, acrylonitrile elastomers,
silicone rubber, polysiloxanes, polyester rubber,
diisocyanate-linked condensation elastomer, EPDM
(ethylene-propylene diene rubbers), chlorosulphonated polyethylene,
fluorinated hydrocarbons, thermoplastic elastomers such as (AB) and
(ABA) type of block copolymers of styrene and butadiene or
isoprene, and (AB)n type of multi-segment block copolymers of
polyurethane or polyester, and the like. In the case that
carboxyl-terminated butadiene-acrylonitrile (CTBN) is used as the
functionalized elastomer, the preferable nitrile content is from
12-35% by weight, more preferably from 20-33% by weight.
[0066] An example of a preferred epoxide-functionalized
epoxy/elastomer adduct is sold in admixture with an epoxy resin
under the trade name HyPox.TM. RK84 (FIG. 5), a bisphenol A epoxy
resin modified with CTBN elastomer, and the trade name HyPox.TM.
RA1340 (FIG. 6), an epoxy phenol novolac resin modified with CTBN
elastomer, both commercially available from CVC Thermoset
Specialties, Moorestown, N.J. In addition to bisphenol A epoxy
resins, other epoxy resins can be used to prepare the
epoxy/elastomer adduct, such as n-butyl glycidyl ether, styrene
oxide and phenylglycidyl ether; bifunctional epoxy compounds such
as bisphenol A diglycidyl ether, bisphenol F diglycidyl ether,
bisphenol S diglycidyl ether and diglycidyl phthalate;
trifunctional compounds such as triglycidyl isocyanurate,
triglycidyl p-aminophenol; tetrafunctional compounds such as
tetraglycidyl m-xylene diamine and
tetraglycidyldiaminodiphenylmethane; and compounds having more
functional groups such as cresol novolac polyglycidyl ether, phenol
novolac polyglycidyl ether and so on. Examples of additional or
alternative epoxy/elastomer and other adducts suitable for use in
the present invention are disclosed in U.S. Pat. No. 6,846,559 and
U.S. Patent Publication 2004/0204551 to Czaplicki, Michael both of
which are incorporated herein by reference.
[0067] Amine Compound Plus Reactive Dispersant
[0068] To prepare the curing agent, in one non-limiting process,
the selected amine compound and the epoxide-functionalized reactive
dispersant are first allowed to react to ensure the dispersant is
fully incorporated. The reactive dispersant is dissolved in a
selected solvent system and allowed to react using a combination of
heating and stirring from about 2 min to about 3 h, preferably from
about 4 min to about 2 h, and most preferably from about 5 min to
about 1 h. Thus, the reaction temperature which can be employed in
the present invention is typically 40.degree. C. to 90.degree. C.,
preferably 50.degree. C. to 80.degree. C., and the concentration of
the starting materials, i.e. the amine compound and the
epoxide-functionalized reactive dispersant, is typically about 2 to
40% by weight, preferably about 5 to 30% by weight. The amount of
reactive dispersant is from about 1 to 70% (w/w) based on the
combined weights of the reactive dispersant and amine compound,
preferably from about 5 to 50% (w/w) based on the combined weights
of the reactive dispersant and amine compound and most preferably
from about 9 to 35% (w/w) based on the combined weights of the
reactive dispersant and amine compound. In the special case where
the epoxide-functionalized reactive dispersant contains a residual
epoxy compound that is not bonded to the elastomer, such as in
FIGS. 5 and 6, an additional purification step is undertaken which
consists of removing the unreacted epoxy compound from said
reactive dispersant. This purification step is especially important
to avoid the formation of aggregates and lumps of solid material
after the addition of the epoxy compound (see below).
[0069] Epoxy Compatible Material
[0070] The epoxy compatible material is any epoxy-functional
material that contains a functional group or groups that are
compatible with an epoxy resin. One example are the
epoxide-functionalized epoxy/elastomer adducts that are sold as
admixtures with an epoxy resin, available commercially under the
trade name HyPox.TM. RK84 (FIG. 5) and the trade name HyPox RA1340
(FIG. 6), from CVC Thermoset Specialties, Moorestown, N.J. Said
HyPox elastomers contain the epoxy compatibilizing monomer
acrylonitrile. Other examples would include, but are not limited
to, epoxy-functional polyacrylates that would contain epoxy
compatible co-monomers, like acrylonitrile and methyl
methacrylate.
[0071] Amine Compound Plus Epoxide-Functionalized Reactive
Dispersant Plus Epoxy Compound, Formation of the Un-Encapsulated
Particles.
[0072] After the amine compound has been allowed to react with the
epoxide-functionalized dispersant, the formation of the
un-encapsulated latent hardener particles begins with the addition
of the epoxy compound. A solution of the epoxy compound is slowly
added to the stirred heated solution of the amine
compound-dispersion stabilizer solution over the course from about
5 min to 6 h, preferably from about 10 min to 4 h, and most
preferably from about 15 min to 2 h, using an apparatus that allows
for a constant uninterrupted addition of epoxy resin solution, such
as a syringe pump or peristaltic pump or the like. The amount of
epoxy compound is from about 10 to 90% (w/w) based on the combined
weights of the amine compound, reactive dispersant, and epoxy
compound, preferably from about 30 to 85% (w/w) based on the
combined weights of the amine compound, reactive dispersant, and
epoxy compound, and most preferably from about 50 to 80% (w/w)
based on the combined weights of the amine compound, reactive
dispersant, and epoxy compound. In one example, a solution of the
reactive dispersant and the amine is agitated, while heating, under
an inert atmosphere and after a predetermined time, a solution of
epoxy compound is added over a predetermined time. The originally
clear solution will become opaque as the epoxy compound begins to
react. As the reaction progresses, the opaqueness of the reaction
system gradually increases, with a characteristic milky white
turbid dispersion eventually occurring.
[0073] When the reaction temperature and the concentration of the
starting materials are too high, aggregates may easily form even in
the presence of a suitable amount of the reactive dispersant. Thus,
the reaction temperature which can be employed in the present
invention is typically 40.degree. C. to 90.degree. C., preferably
50.degree. C. to 80.degree. C., and the concentration of the
starting materials, i.e. the amine compound, the reactive
dispersant, and epoxy compound, is typically 2 to 40% by weight,
preferably 5 to 30% by weight. Generally, the particle size of the
adduct increases with increased concentrations of the starting
materials but decreases with increased concentrations of the
reactive dispersant.
[0074] Encapsulation
[0075] The particles are subsequently encapsulated, with each layer
of encapsulate or protective shell applied over the particle in two
or more successive steps. Various known methods for encapsulating
spherical curing agents may be used in this invention. In one
embodiment, the adduct particles may be reacted with an
encapsulation agent to form two or more protective shells, where
said encapsulating agent is comprised of a polyfunctional
isocyanate compound or a mixture of polyfunctional isocyanate
compounds and multifunctional epoxy compounds or a mixture of
polyfunctional isocyanate and epoxy compatible compound (e.g.,
acrylonitrile), or a mixture of a polyfunctional isocyanate, epoxy
compounds, and epoxy compatible compound. Suitable polyfunctional
isocyanate compounds include the mononuclear and polynuclear
species of toluene diisocyanate, methylene diphenyl diisocyanate,
hydrogenated methylene diphenyl diisocyanate, 1,5-naphthalene
diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate,
xylylene diisocyanate, hydrogenated xylylene diisocyanate,
tetramethylxylene diisocyanate, 1,3,6-hexamethylene triisocyanate,
lysine diisocyanate, triphenylethane triisocyanate, polyfunctional
isocyanate compounds formed by addition of such compounds and other
active hydrogen-containing compound, and any mixtures thereof.
[0076] Representative examples of multifunctional epoxies include
methylene bisglycidyl aniline, HELOXY.TM. Modifier 48 (a product of
Hexion Specialty Chemicals), Toagosei GP-301 graft
polymethylmethacrylate-g-epoxy modified acrylate polymer, and a
multi-functional epoxy containing acrylonitrile (epoxy compatible
co-monomer) but other multifunctional epoxies should also work.
[0077] The amount of the encapsulation agent employed to
encapsulate the un-encapsulated particles affects the storage
stability and the curability of a curing agent masterbatch. With
the same particles of the addition product, increased amounts of
the encapsulation agent improve the storage stability, but lower
the curability. Thus, for adduct particles having a diameter of
about 0.1 micron to 30 micron, the encapsulation agent is employed
in ratio from about 50:50 to 95:5 (w/w) core particles to
encapsulation agent, preferably from about 60:40 to 90:10 (w/w)
core particles to encapsulation agent, and most preferably in a
ratio from about 70:30 to 90:10 (w/w) core particles to
encapsulation agent. Additionally, when the encapsulation agent is
a mixture of isocyanate compounds and epoxy compounds or isocyanate
compounds and epoxy compatible compounds, the amount of epoxy
compound is used in a ratio from about 1:99 to 99:1 (w/w)
isocyanate compounds to epoxy compounds, preferably from about
60:40 to 99:1 (w/w) isocyanate compounds to epoxy compounds, and
most preferably in a ratio from about 80:20 and 99:1 (w/w)
isocyanate compounds to epoxy compounds. Additionally, when the
encapsulation agent is a mixture of isocyanate compounds, epoxy
compounds, and epoxy compatible compounds, the amount of epoxy
compound is used in a ratio from about 1:99 to 99:1 (w/w)
isocyanate compounds to epoxy compounds, preferably from about
60:40 to 99:1 (w/w) isocyanate compounds to epoxy compounds plus
epoxy compatible compounds, and most preferably in a ratio from
about 80:20 and 99:1 (w/w) isocyanate compounds to epoxy compounds.
Thus, the compromise between storage stability and curability
varies depending on the size of the adduct particle, with smaller
particle sizes requiring increased amounts of shell forming
material such as polyfunctional isocyanate to achieve the same
release or barrier properties.
[0078] In one embodiment, when the particle forming reaction is
completed, the un-encapsulated particles are isolated from the
reaction medium by filtration and then washed with fresh solvent.
The particles are then subsequently encapsulated.
[0079] Masterbatch
[0080] In general, to form the masterbatch, the encapsulated
particles are uniformly dispersed in an epoxy resin in a range from
about 5 to 90% (w/w) based on the combined weights of the particles
and epoxy resin, preferably in the range of about 15 to 80% (w/w)
based on the combined weights of the particles and liquid epoxy
compound, and most preferably in the range of about 20 to 70% (w/w)
based on the combined weights of the particles and liquid epoxy
compound.
[0081] In one embodiment, the epoxy resin can be one or more epoxy
resins of bisphenol A, bisphenol F, novolac epoxies, and the
like.
[0082] In one embodiment, to avoid the formation of secondary
particles, the encapsulated particles are mechanically dispersed in
the epoxy resin as primary particles, for example, by blending with
a three roll mill.
[0083] In another embodiment, after the encapsulation process is
completed, heating and stirring are stopped and an epoxy resin is
added to the dispersion. The mixture is again stirred, enough to
distribute the epoxy resin equally in the dispersion. The solvent
is then removed, using vacuum distillation, or the like, such that
the total solid content is about 60 to 100% (w/w), preferably about
70 to 100% (w/w), and most preferably about 80 to 100% (w/w). The
particles are then dispersed further in the epoxy resin using
techniques known to those of ordinary skill in the art, such as a
three-roll mill, or the like.
[0084] In yet another embodiment, when the reaction is completed,
the solvent is removed using vacuum distillation to 100% (w/w)
solids content. The solid particles are then added to an epoxy
resin and the particles dispersed further in epoxy resin using
techniques known to those of ordinary skill in the art, such as a
three-roll mill, or the like.
[0085] In still yet another embodiment, when the reaction is
completed, the particles are separated by filtering the dispersion
of the particles. Fresh solvent is used to wash off unreacted
starting material adhered to the surface of the particles. An epoxy
resin is then added to the solid particles and the mixture
dispersed further using techniques known to those of ordinary skill
in the art, such as a three-roll mill, or the like.
[0086] The adhesive compositions disclosed herein are potentially
useful in various applications including in a conducting adhesive,
composite, molding compound, anisotropic conducting film (ACF)
adhesive, non-random array ACF, non-conductive adhesive film (NCF),
coating, encapsulant, underfill material, lead-free solder,
etc.
[0087] Having described the invention in detail, the invention will
be illustrated by the following non-limiting examples:
EXAMPLES
Examples for the Formation of the Un-Encapsulated Core
Particles
Example 1
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (1)
[0088] Commercial material HyPox RK84 [a commercial material of CVC
Thermoset Specialties and mixture of a bisphenol A epoxy resin and
its adduct with CTBN (FIG. 5)] was used as the dispersion
stabilizer. A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet was charged
with 0.93 g of the CTBN-epoxy adduct, 1.64 g (0.02 mole) of
2-methylimidazole and 48 g of 4-methyl-2-pentanone (MIBK). The
reactor was placed in an 80.degree. C. bath and purged with argon.
After 1 h, a solution of 3.39 g (0.019 equivalent weight) DER.TM.
332 (a product of Dow Chemical) and 3.4 g of MIBK was added
dropwise over the course of 20 min, after which the reaction was
allowed to stir at 300 rpm for 6 hr under an argon atmosphere. A
white milky dispersion was formed. The dispersion was discharged
from the reactor, centrifuged, washed with MIBK, and evaporated to
dryness to afford 3.6 g (60.4% yield) of product. A small drop of
the dispersion was diluted, coated on glass slide and dried in
vacuum at room temperature. The dried sample was sputtered with a
thin layer of gold and the scanning electron micrograph of this
taken using a Hitachi S-2460N scanning electron microscope.
Example 2
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (2)
[0089] A CTBN-epoxy adduct that was isolated from CVC Thermoset
Specialties HyPox.TM. RK84 was used as the dispersion stabilizer.
The adduct was obtained by dissolving the material in methyl ethyl
ketone, followed by precipitation with methanol, and repeating the
process two more times. The un-encapsulated core particles 2 were
synthesized from 0.51 g of the CTBN-epoxy adduct, 1.63 g (0.02
mole) of 2-methylimidazole, 3.51 g (0.02 equivalent weight) DER.TM.
332 and 51 g of MIBK using the procedure of Example 1 to afford 4.4
g (78% yield) of particles.
Example 3
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RA 1340 (3)
[0090] Commercial material HyPox RA1340 [a commercial material of
CVC Thermoset Specialties and mixture of diglycidyl ether of
bisphenol A and its adduct with CTBN (FIG. 6)] was used as the
dispersion stabilizer. The microcapsule core 3 was synthesized from
1.15 g of the aforementioned CTBN-epoxy adduct, 1.64 g (0.02 mole)
of 2-methylimidazole, 2.87 g (0.0164 equivalent weight) DER.TM. 332
and 51 g of MIBK using the procedure of Example 1 to afford 1.2 g
(21.2% yield) of particles.
Example 4
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RA 1340 (4)
[0091] A CTBN-epoxy adduct isolated from CVC Thermoset Specialties
HyPox.TM. RA 1340 was used as the dispersion stabilizer. The adduct
was obtained by first dissolving the material in methyl ethyl
ketone, followed by precipitation with methanol, and repeating the
process two more times. The un-encapsulated core particles 4 were
synthesized from 0.53 g of the CTBN-adduct, 1.65 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, and
51 g of MIBK using the procedure as described in Example 1 to
afford 2.6 g (45.9% yield) of particles.
Example 5
Synthesis of Un-Encapsulated Core Particles from
2-Ethyl-4-Methylimidazole, DGEBA, and HyPox.TM. RK 84 (5)
[0092] The un-encapsulated core particles 5 were synthesized from
0.57 g of the CTBN-epoxy adduct of Example 2, 2.20 g (0.02 mole) of
2-ethyl-4-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM.
332, and 63 g of MIBK using the procedure of Example 1 to afford
0.7 g (11.2% yield) of particles.
Example 6
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RA 1340 (6)
[0093] The un-encapsulated core particles 6 were synthesized from
0.26 g of the CTBN-epoxy adduct of Example 4, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, and
50 g of MIBK using the procedure of Example 1 to afford 1.6 g
(26.9% yield) of particles.
Example 7
Synthesis of Un-Encapsulated Core Particles from
2-Ethyl-4-Methylimidazole, DGEBA, and HyPox.TM. RK 84 (7)
[0094] The un-encapsulated core particles 7 were synthesized from
0.57 g of the CTBN-epoxy adduct of Example 2, 2.20 g (0.02 mole) of
2-ethyl-4-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM.
332 and 56 g of MIBK using the procedure of Example 1 and the
reaction was allowed to stir at 300 rpm for 16.5 h under an argon
atmosphere to afford 2.5 g (40% yield) of particles.
Example 8
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (8)
[0095] The microcapsule core 8 was synthesized from 0.52 g of the
CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, and
51 g of MIBK using the procedure of Example 1. The reaction was
allowed to stir at 300 rpm for 16 h under an argon atmosphere to
afford 4.0 g (71% yield) of particles.
Example 9
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (9)
[0096] The un-encapsulated core particles 9 were synthesized from
0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, and
52 g of MIBK using the procedure of Example 1. The reaction was
allowed to stir at 1000 rpm for 6 h under an argon atmosphere to
afford 4.18 g (74% yield) of particles.
Example 10
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (10)
[0097] The un-encapsulated core particles 10 were synthesized from
0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole and 37.3 g of 4-methyl-2-pentanone (MIBK). The
reactor was placed in an 80.degree. C. bath and purged with argon.
After 1 h, a solution of 3.5 g (0.02 equivalent weight) DER.TM. 332
(a product of Dow Chemical) and 3.5 g of MIBK was added dropwise
over the course of 15 min, after which the reaction was allowed to
stir at 1000 rpm for 1 h under an argon atmosphere. After this, 10
g of heptane was added dropwise over the course of 1 h. The
reaction was allowed to stir at 1000 rpm for another 4 h. A white
milky dispersion was formed. The dispersion was discharged,
centrifuged, washed with MIBK, and evaporated to dryness to afford
2.1 g (37% yield) of dried particles.
Example 11
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (11)
[0098] The un-encapsulated core particles 11 were synthesized from
0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, and 37.3 g of 4-methyl-2-pentanone (MIBK). The
reactor was placed in an 80.degree. C. bath and purged with argon.
After 1 h, a solution of 3.5 g (0.02 equivalent weight) DER.TM. 332
(a product of Dow Chemical) and 3.5 g of MIBK was added dropwise
over the course of 15 min, after which the reaction was allowed to
stir at 1000 rpm for 1 h under an argon atmosphere, after which 3 g
of heptane was added drop wise over the course of 1 h. The reaction
was allowed to stir at 1000 rpm for 4 h. A white milky dispersion
was formed. The dispersion was discharged, centrifuged, washed with
MIBK, and evaporated to dryness to afford 3.0 g (53% yield) of
dried particles.
Example 12
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (12)
[0099] The un-encapsulated core particles 12 were synthesized from
1.05 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, and
51 g of MIBK using the procedure of Example 1. The reaction was
allowed to stir at 1000 rpm for 6 h to afford 4.4 g (71% yield) of
particles.
Example 13
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (13)
[0100] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet. The flask
was charged with 0.52 g of the CTBN-epoxy adduct of Example 2, 1.64
g (0.02 mole) of 2-methylimidazole, 5.1 g of heptane and 42.3 g of
4-methyl-2-pentanone (MIBK). The reaction flask was placed in an
80.degree. C. bath and purged with argon. After 1 h, a solution of
3.5 g (0.02 equivalent weight) DER.TM. 332 (a product of Dow
Chemical) and 3.6 g of MIBK was added dropwise over the course of
15 min, after which the reaction was allowed to stir at 1000 rpm
for 6 h. A white milky dispersion was formed. The dispersion was
discharged, centrifuged, washed with MIBK, and evaporated to
dryness to afford 3.4 g (60% yield) of particles.
Example 14
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and "Purified" HyPox.TM. RK 84 (14)
[0101] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet was charged
with 0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02
mole) of 2-methylimidazole, 5.1 g of heptane and 46.8 g of
4-methyl-2-pentanone (MIBK). The reactor was placed in an
80.degree. C. bath and purged with argon and stirred for 1 h at 300
rpm. A solution of 3.5 g (0.02 equivalent weight) DER.TM. 332 (a
product of Dow Chemical) and 3.5 g of MIBK was added dropwise over
the course of 15 min, after which the reaction was allowed to stir
at 300 rpm for 1 hr and then at 1000 rpm for another 5 h. A white
milky dispersion was formed. The dispersion was discharged,
centrifuged, washed with MIBK and evaporated to dryness to afford
3.2 g (57% yield) of particles.
Example 15
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (15)
[0102] The un-encapsulated core particles (15) were synthesized
from 0.51 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02
mole) of 2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM.
332, 15.3 g of heptane and 34 g of MIBK using the procedure of
Example 13. The reaction was allowed to stir at 1000 rpm for 6 h
under an argon atmosphere to afford 4.5 g (80% yield) of
particles.
Example 16
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (16)
[0103] The un-encapsulated core particles 16 were synthesized from
0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, 2.6
g of heptane and 49 g of MIBK using the procedure of Example 13 and
the reaction was allowed to stir at 1000 rpm for 6 h under an argon
atmosphere to afford 2.4 g (42.4% yield) of particles.
Example 17
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (17)
[0104] The un-encapsulated core particles 17 were synthesized from
0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, 10.2
g of heptane and 41 g of MIBK using the procedure of Example 13.
The reaction was allowed to stir at 1000 rpm for 6 h under an argon
atmosphere to afford 3.9 g (69% yield) of particles.
Example 18
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (18)
[0105] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet was charged
with 0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02
mole) of 2-methylimidazole, and 47.3 g of 4-methyl-2-pentanone
(MIBK). The reactor was placed in an 80.degree. C. bath, and purged
with argon. After the reaction was allowed to stir at 300 rpm for 1
hr, a solution of 3.5 g (0.02 equivalent weight) DER.TM. 332 (a
product of Dow Chemical) and 3.5 g of MIBK was added dropwise over
the course of 15 min, after which the reaction was allowed to stir
at 300 rpm for 1 h and then 1000 rpm for another 5 h. A white milky
dispersion was formed. The dispersion was discharged, centrifuged,
washed with MIBK, and evaporated to dryness to afford 4.53 g (80%
yield) of particles.
Example 19
Synthesis Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (19)
[0106] The un-encapsulated core particles 19 were synthesized from
0.51 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, and
51 g of MIBK using the procedure of Example 13 and the reaction was
allowed to stir at 1500 rpm for 6 h under an argon atmosphere to
afford 4.05 g (71.5% yield) of particles.
Example 20
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (20)
[0107] The un-encapsulated core particles 20 were synthesized from
0.52 g of the CTBN-epoxy adduct of Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332, 7.6
g of heptane, and 43 g of MIBK using the procedure of Example 13
and the reaction was allowed to stir at 1000 rpm for 6 h to afford
4.05 g (71.5% yield) of particles.
Example 21
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (21)
[0108] The un-encapsulated core particles 21 were synthesized from
0.51 g of the CTBN-epoxy adduct from Example 2, 1.65 g (0.02 mole)
of 2-methylimidazole, 3.5 g (0.02 equivalent weight) DER.TM. 332,
7.6 g of heptane and 43 g of MIBK using the procedure of Example
13. The reaction was allowed to stir at 1000 rpm for 16 h to afford
3.6 g (64% yield) of particles.
Example 22
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (22)
[0109] The un-encapsulated core particles 22 were synthesized from
0.51 g of the CTBN-epoxy adduct from Example 2, 1.64 g (0.02 mole)
of 2-methylimidazole, 3.85 g (0.022 equivalent weight) DER.TM. 332,
7.6 g of heptane, and 43 g of MIBK using the procedure of Example
13. The reaction was allowed to stir at 1000 rpm for 6 h under an
argon atmosphere to afford 4.95 g (82.3% yield) of particles. A
small drop of the dispersion was diluted with MIBK, coated on glass
slide, and dried under vacuum at room temperature. The dried sample
was sputtered with a thin layer of gold and its electron micrograph
(FIG. 1 and FIG. 2) taken with a Hitachi S-2460N scanning electron
microscope.
Example 23
Synthesis of Un-Encapsulated Core Particles from 2-Methylimidazole,
DGEBA, and HyPox.TM. RK 84 (23)
[0110] The un-encapsulated core particles 23 were synthesized from
0.51 g of the CTBN-epoxy adduct from Example 2, 1.64 g (0.02 mole)
of 2-methylimidazole, 3.85 g (0.022 equivalent weight) DER.TM. 332,
7.6 g of heptane and 42 g of MIBK using the procedure of Example
13. The reaction was allowed to stir at 1000 rpm for 16 h to afford
4.49 g (74.7% yield) of particles.
Examples for the Encapsulation of the Un-Encapsulated Core
Particles
Example 24
Encapsulated Particles from 2-Methylimidazole, DGEBA, HyPox.TM. RK
84, and MDI (24)
[0111] The microcapsule core was synthesized from 0.52 g of the
CTBN-epoxy adduct from Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.85 g (0.022 equivalent weight) DER.TM. 332,
7.6 g of heptane and 42 g of MIBK using the procedure of Example
13. The reaction was allowed to stir at 1000 rpm for 6 h under an
argon atmosphere. A small drop of the dispersion was removed,
diluted with MIBK, coated on glass slide, and dried under vacuum at
room temperature. The dried sample was sputter-coated with a thin
layer of gold and the electron micrograph taken with a Hitachi
S-2460N scanning electron microscope. The encapsulation was started
by adding a solution of 1.56 g (0.0125 equivalent weight) of
4,4'-Methylenebis(phenyl isocyanate), most commonly referred to as
MDI, and 14.1 g of MIBK, which was added dropwise over the course
of 110 min, after which the reaction was allowed to stir at 1000
rpm for 15 h under an argon atmosphere. A small drop of the
dispersion was dried and its FT-IR spectrum showed complete
conversion of the isocyanate moiety. After it was confirmed all of
the isocyanate had been consumed, a small drop of the dispersion
was removed, diluted with additional MIBK, coated on glass slide,
and dried under vacuum at room temperature. The dried sample was
sputtered with a thin layer of gold and its electron micrograph
taken with a Hitachi S-2460N scanning electron microscope (FIG. 3
and FIG. 4).
Example 25
Synthesis Microcapsules from 2-Methylimidazole, DGEBA, HyPox.TM. RK
84, MDI, and 4,4'-Methylenebis(N,N-diglycidylaniline) (25)
[0112] The microcapsule core was synthesized from 0.51 g of the
CTBN-epoxy adduct from Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.85 g (0.022 equivalent weight) DER.TM. 332,
7.6 g of heptane and 42 g of MIBK using the procedure of Example 13
and the reaction was allowed to stir at 1000 rpm for 6 hr under an
argon atmosphere. The encapsulation was started by adding a
solution of 1.4 g (0.0112 equivalent weight) of MDI, 0.16 g
(0.00038 equivalent weight) of
4,4'-Methylenebis(N,N-diglycidylaniline), and 14.1 g of MIBK, which
was added dropwise over the course of 110 min, after which the
reaction was allowed to stir at 1000 rpm for 15 h under an argon
atmosphere. A small drop of dispersion was dried and its FT-IR
spectrum showed complete conversion of the isocyanate moiety.
Example 26
Synthesis of Microcapsules from 2-Methylimidazole, DGEBA, HyPox.TM.
RK 84, and MDI (26)
[0113] The microcapsule core was synthesized from 0.52 g of the
CTBN-epoxy adduct from Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.86 g (0.022 equivalent weight) DER.TM. 332,
7.6 g of heptane, and 42 g of MIBK using the procedure of Example
13. The reaction was allowed to stir at 1000 rpm for 6 h under an
argon atmosphere. The encapsulation was performed by the addition
of a solution of 1.57 g (0.0125 equivalent weight) of MDI and 14.1
g of MIBK, which was added dropwise over the course of 90 min,
after which the reaction was allowed to stir at 1000 rpm for 15 h
under an argon atmosphere. A small drop of dispersion was dried and
its FT-IR spectrum showed complete conversion of the isocyanate
moiety.
Example 27
Synthesis of Microcapsules from 2-Methylimidazole, DGEBA, HyPox.TM.
RK 84, MDI, and 4,4'-Methylenebis(N,N-diglycidylaniline) (27)
[0114] The microcapsule core was synthesized from 0.52 g of the
CTBN-epoxy adduct from Example 2, 1.64 g (0.02 mole) of
2-methylimidazole, 3.85 g (0.022 equivalent weight) DER.TM. 332,
7.6 g of heptane and 43 g of MIBK using the procedure of Example 13
and the reaction was allowed to stir at 1000 rpm for 6 hr under an
argon atmosphere. The encapsulation was started by adding a
solution of 2.8 g (0.0223 equivalent weight) of MDI (a product of
Sigma Aldrich), 0.35 g (0.0033 equivalent weight) of
4,4'-Methylenebis(N,N-diglycidylaniline), and 14.1 g of MIBK, which
was added dropwise over the course of 240 min, after which the
reaction was allowed to stir at 1000 rpm for 15 h under an argon
atmosphere.
Example 28
Synthesis of Microcapsules from 2-Methylimidazole, DGEBA, HyPox.TM.
RK 84, MDI, and 4,4'-Methylenebis(N,N-diglycidylaniline) (28)
[0115] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet was charged
with 1.03 g of the CTBN-epoxy adduct from Example 2, 3.28 g (0.04
mole) of 2-methylimidazole, 15.2 g of heptane and 76 g of
4-methyl-2-pentanone (MIBK). The reactor was placed in an
80.degree. C. bath and purged with argon. After 1 hr, a solution of
7.7 g (0.044 equivalent weight) DER.TM. 332 (a product of Dow
Chemical) and 7.7 g of MIBK was added drop wise over the course of
40 min, after which the reaction was allowed to stir at 1000 rpm
for 6 hr under an argon atmosphere. A white milky dispersion was
formed. A small drop of the dispersion was diluted, coated on glass
slide and dried in vacuum oven at room temperature. The dried
sample was sputtered with a thin layer of Au and taken scanning
electron micrographs. The encapsulation was started by adding a
solution of 2.8 g (0.0223 equivalent weight) of MDI, 0.32 g (0.003
equivalent weight) of 4,4'-Methylenebis(N,N-diglycidylaniline), and
28.2 g of MIBK, which was added dropwise over the course of 240
min, after which the reaction was allowed to stir at 1000 rpm for
12.5 hr under an argon atmosphere.
Example 29
Synthesis of Microcapsules from 2-Methylimidazole, DGEBA, HyPox.TM.
RK 84L, Desmodur.RTM. W, and
4,4'-Methylenebis(N,N-Diglycidylaniline) (29)
[0116] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet was charged
with 2.09 g of the CTBN-epoxy adduct from Example 2, 6.56 g (0.08
mole) of 2-methylimidazole and 183 g of 4-methyl-2-pentanone
(MIBK). The reactor was placed in an 80.degree. C. bath and purged
with argon. After 1 hr, a solution of 15.4 g (0.088 equivalent
weight) DER.TM. 332 (diglycidyl ether of bisphenol A (DGEBA) from
Dow Chemical) and 18.7 g of MIBK was added drop wise over the
course of 1 hr, after which the reaction was allowed to stir at
1000 rpm for 6 hr under an argon atmosphere. A white milky
dispersion was formed. The particles were allowed to precipitate
under gravity allowing the supernatant liquid was removed by
decantation. The particles were redispersed in MIBK. The residual
dispersion was filtered through a small pore size membrane filter.
The particles were redispersed in MIBK and then filtered through a
30 .mu.m pore size filter to remove large-sized particles and
aggregates. A few drops of the resulting dispersion were dried,
sputtered with gold, loaded into an SEM. Its micrograph showed the
particles were of adequate quality to be allowed to proceed on to
the encapsulation step. The solid content of the dispersion was
measured at 9.84% (w/w). The yield of total dispersion was 84.4
g.
[0117] A three-neck round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet was charged
with 0.83 g of the CTBN-epoxy adduct from Example 2, 10.3 g of
MIBK, and the purified dispersion. The reactor was placed in an
80.degree. C. bath and purged with argon. To this, 17 g of heptane
was added drop-wise over the course of 1 hr. The encapsulation was
started by adding a solution of 1.9 g (0.0145 equivalent weight) of
Desmodur.RTM. W (a liquid cycloaliphatic diisocyanate from Bayer
MaterialScience), 0.19 g (0.002 equivalent weight) of
4,4'-Methylenebis(N,N-diglycidylaniline), and 18.9 g of MIBK, which
was added drop-wise over the course of 4 hr, after which the
reaction was allowed to stir at 1000 rpm for 12.5 hr under an argon
atmosphere.
Example 30 (Prophetic)
Synthesis of Microcapsules Comprised of Two Shell Materials
[0118] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet is charged
with 2.09 g of the CTBN-epoxy adduct from Example 2, 6.56 g (0.08
mole) of 2-methylimidazole and 183 g of 4-methyl-2-pentanone
(MIBK). The reactor is placed in an 80.degree. C. bath and purged
with argon. After 1 hr, a solution of 15.4 g (0.088 equivalent
weight) DER.TM. 332 (a product of Dow Chemical) and 18.7 g of MIBK
is added drop-wise over the course of 1 hr, after which the
reaction is allowed to stir at 1000 rpm for 6 hr under an argon
atmosphere. A white milky dispersion is formed. The particles are
allowed to precipitate under gravity allowing the supernatant
liquid to be removed by decantation. The particles are redispersed
in MIBK. The residual dispersion is filtered through a small pore
size membrane filter. The particles are redispersed in MIBK and
then filtered through a 30 .mu.m pore size filter to remove
large-sized particles and aggregates.
[0119] A three-neck round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet is charged
with 0.83 g of the CTBN-epoxy adduct from Example 2, 10.3 g of
MIBK, and the purified dispersion. The reactor is placed in an
80.degree. C. bath and purged with argon. To this, 17 g of heptane
is added drop-wise over the course of 1 hr. The encapsulation with
the first shell layer was started by adding a solution of 1.9 g
(0.0145 equivalent weight) of Desmodur.RTM. W (a product of Bayer
MaterialScience), 0.19 g (0.002 equivalent weight) of
4,4'-Methylenebis(N,N-diglycidylaniline), and 18.9 g of MIBK is
added drop-wise over the course of 4 hr, after which the reaction
is allowed to stir at 1000 rpm for 12.5 hr under an argon
atmosphere.
[0120] The second shell layer is formed by the addition of a
solution of 1.9 g (0.0145 equivalent weight) of Desmodur.RTM. W (a
product of Bayer MaterialScience), 0.19 g (0.002 equivalent weight)
of 4,4'-Methylenebis(N,N-diglycidylaniline), and 18.9 g of MIBK is
added drop-wise over the course of 4 hr, after which the reaction
is allowed to stir at 1000 rpm for 12.5 hr under an argon
atmosphere.
Example 31 (Prophetic)
Synthesis of Microcapsules Comprised of Two Shell Materials, Where
the Outermost Shell Material is Comprised of an Epoxy Compatible
Material
[0121] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet is charged
with 2.09 g of the CTBN-epoxy adduct from Example 2, 6.56 g (0.08
mole) of 2-methylimidazole and 183 g of 4-methyl-2-pentanone
(MIBK). The reactor is placed in an 80.degree. C. bath and purged
with argon. After 1 hr, a solution of 15.4 g (0.088 equivalent
weight) DER.TM. 332 (a product of Dow Chemical) and 18.7 g of MIBK
is added drop-wise over the course of 1 hr, after which the
reaction is allowed to stir at 1000 rpm for 6 hr under an argon
atmosphere. A white milky dispersion is formed. The particles are
allowed to precipitate under gravity allowing the supernatant
liquid to be removed by decantation. The particles are redispersed
in MIBK. The residual dispersion is filtered through a small pore
size membrane filter. The particles are redispersed in MIBK and
then filtered through a 30 .mu.m pore size filter to remove
large-sized particles and aggregates.
[0122] A three-neck round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet is charged
with 0.83 g of the CTBN-epoxy adduct from Example 2, 10.3 g of
MIBK, and the purified dispersion. The reactor is placed in an
80.degree. C. bath and purged with argon. To this, 17 g of heptane
is added drop-wise over the course of 1 hr. The first shell layer
encapsulation was started by adding a solution of 1.9 g (0.0145
equivalent weight) of Desmodur.RTM. W (a product of Bayer
MaterialScience), 0.19 g (0.002 equivalent weight) of
4,4'-Methylenebis(N,N-diglycidylaniline), and 18.9 g of MIBK is
added drop-wise over the course of 4 hr, after which the reaction
is allowed to stir at 1000 rpm for 12.5 hr under an argon
atmosphere.
[0123] The second shell layer is formed by the addition of a
solution of 1.9 g (0.0145 equivalent weight) of Desmodur.RTM. W (a
product of Bayer MaterialScience), 1.9 g of CVC Thermoset Materials
HyPox.TM. RA1340, and 18.9 g of MIBK is added drop-wise over the
course of 4 hr, after which the reaction is allowed to stir at 1000
rpm for 12.5 hr under an argon atmosphere.
Example 32 (Prophetic)
Synthesis of Microcapsules Comprised of Two Shell Materials, Where
the Outermost Shell Material is Comprised of an Epoxy Compatible
Material
[0124] A three-necked round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet is charged
with 2.09 g of the CTBN-epoxy adduct from Example 2, 6.56 g (0.08
mole) of 2-methylimidazole and 183 g of 4-methyl-2-pentanone
(MIBK). The reactor is placed in an 80.degree. C. bath and purged
with argon. After 1 hr, a solution of 15.4 g (0.088 equivalent
weight) DER.TM. 332 (a product of Dow Chemical) and 18.7 g of MIBK
is added drop-wise over the course of 1 hr, after which the
reaction is allowed to stir at 1000 rpm for 6 hr under an argon
atmosphere. A white milky dispersion is formed. The particles are
allowed to precipitate under gravity allowing the supernatant
liquid to be removed by decantation. The particles are redispersed
in MIBK. The residual dispersion is filtered through a small pore
size membrane filter. The particles are redispersed in MIBK and
then filtered through a 30 .mu.m pore size filter to remove
large-sized particles and aggregates.
[0125] A three-neck round bottom flask, equipped with a PTFE
fluoropolymer half moon-shaped overhead stirrer, a reflux
condenser, an addition funnel, and an argon gas inlet is charged
with 0.83 g of the CTBN-epoxy adduct from Example 2, 10.3 g of
MIBK, and the purified dispersion. The reactor is placed in an
80.degree. C. bath and purged with argon. To this, 17 g of heptane
is added drop-wise over the course of 1 hr. The encapsulation was
started by adding a solution of 1.9 g (0.0145 equivalent weight) of
Desmodur.RTM. W (a product of Bayer MaterialScience), 0.19 g (0.002
equivalent weight) of 4,4'-Methylenebis(N,N-diglycidylaniline), and
18.9 g of MIBK is added drop-wise over the course of 4 hr, after
which the reaction is allowed to stir at 1000 rpm for 12.5 hr under
an argon atmosphere.
[0126] The second shell layer is formed by the addition of a
solution of 1.9 g (0.0145 equivalent weight) of Desmodur.RTM. W (a
product of Bayer MaterialScience), 1.9 g of Toagosei GP-301 graft
polyacrylate, 0.19 g (0.002 equivalent weight) of
4,4'-Methylenebis(N,N-diglycidylaniline), and 18.9 g of MIBK is
added drop-wise over the course of 4 hr, after which the reaction
is allowed to stir at 1000 rpm for 12.5 hr under an argon
atmosphere.
Examples for the Preparation of the Masterbatch
Example 33
Preparation of the Masterbatch from the Particles of Example 24
[0127] The dispersion of the particles of Example 24 were
evaporated under vacuum at 50.degree. C. to obtain a yellow solid,
ground with a mortar and pestle, and added to diglycidyl ether of
bisphenol A in a ratio of 35:65 (w/w) particles to epoxy resin. The
mixture was dispersed for 20 min using a three roll mill to obtain
a creamy yellow dispersion.
Example 34
Preparation of the Masterbatch from the Particles of Example 28
[0128] At room temperature, 10 g of diglycidyl ether of bisphenol A
was added to the reaction mixture of Example 28, which contained
the dispersion of the particles, and stirred for 3 hr. The solvent
was removed under vacuum at 31.degree. C. to a solids content of
86% (w/w). From this, 12.86 g was removed and mixed with and
additional 7.90 g of diglycidyl ether of bisphenol A. The mixture
was then process further for 3 min using a three-roll mill to
obtain a creamy yellow dispersion.
[0129] Performance Results:
[0130] For the solvent resistance test, mixtures were prepared by
combining the particles, diglycidyl ether of bisphenol A, and MIBK
in a ratio of 4:50:46 (w/w). The mixtures were then placed in a
40.degree. C. oil bath and monitored visually for a change in
viscosity. The results are shown below in Table 1. Aliquots of the
mixtures above were coated on glass slides as thin films and dried
under vacuum at room temperature. DSC traces were obtained using a
TA Instruments Q10 Differential Scanning calorimeter using a
temperature window of 30 to 250.degree. C., a heating rate of
5.degree. C./min, and performed under a nitrogen atmosphere. The
results are shown below in Table 1.
TABLE-US-00001 TABLE 1 The solvent resistance and DSC results of
the un-encapsulated and encapsulated particles: Solvent resistance
and DSC results of the un-encapsulated and encapsulated particles
Solvent DSC Un-encapsulated/ resistance T.sub.peak Particle
Encapsulated Time to gel (h) (exo, .degree. C.) .DELTA.H (J/g) 22
Un-encapsulated 14 105 297 24 Encapsulated 120 119 330 25
Encapsulated 170 124 307 27 Encapsulated 240 142 200 28
Encapsulated 190 124 218
[0131] Having described the invention in detail and by reference to
specific embodiments thereof it will be apparent to those skilled
in the art that numerous variations and modifications are possible
without departing from the spirit and scope of the following
claims.
* * * * *