U.S. patent application number 10/458826 was filed with the patent office on 2004-01-08 for chlorofluoro elastomer compositions for use in electrophotographic fusing applications.
This patent application is currently assigned to Xerox Corporation. Invention is credited to Badesha, Santokh S., Gervasi, David J., Heeks, George J., Henry, Arnold W., Riehle, George A..
Application Number | 20040005421 10/458826 |
Document ID | / |
Family ID | 25095534 |
Filed Date | 2004-01-08 |
United States Patent
Application |
20040005421 |
Kind Code |
A1 |
Gervasi, David J. ; et
al. |
January 8, 2004 |
Chlorofluoro elastomer compositions for use in electrophotographic
fusing applications
Abstract
Elastomer compositions comprising a blend of a fluoroelastomer
comprising a terpolymer of vinylidene fluoride, tetrafluoroethylene
and hexafluoropropylene and a chlorofluoroelastomer comprising a
co-or terpolymer of vinylidene fluoride, chlorotrifluoroethylene
and 0-40 mole % of hexafluoropropylene are provided. The
composition may be cured and is particularly suitable for use as a
surface release layer for fusing systems used in
electrostatographic imaging systems.
Inventors: |
Gervasi, David J.; (West
Henrietta, NY) ; Riehle, George A.; (Webster, NY)
; Heeks, George J.; (Rochester, NY) ; Henry,
Arnold W.; (Pittsford, NY) ; Badesha, Santokh S.;
(Pittsford, NY) |
Correspondence
Address: |
Serle Mosoff
PERMAN & GREEN, LLP
425 Post Road
Fairfield
CT
06824
US
|
Assignee: |
Xerox Corporation
|
Family ID: |
25095534 |
Appl. No.: |
10/458826 |
Filed: |
June 11, 2003 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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10458826 |
Jun 11, 2003 |
|
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09772576 |
Jan 30, 2001 |
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Current U.S.
Class: |
428/35.7 ;
524/730 |
Current CPC
Class: |
G03G 15/2025 20130101;
G03G 15/2057 20130101; C08L 27/12 20130101; C08L 2205/02 20130101;
Y10T 428/1352 20150115; C08L 27/12 20130101; C08L 2666/04
20130101 |
Class at
Publication: |
428/35.7 ;
524/730 |
International
Class: |
B65D 001/00 |
Claims
What is claimed is:
1. A process for preparing a cross-linked fuser composition
comprising mixing solutions of a] a fluoroelastomer comprising a
terpolymer of vinylidene fluoride, tetrafluoroethylene and
hexafluoropropylene; and b] a chlorofluoroelastomer comprising a
copolymer or terpolymer of vinylidene fluoride,
chlorotrifluoroehtylene and from 0 to about 40 mole percent of a
monomer selected from the group consisting of hexafluoropropylene
and tetrafluoropropylene; in an appropriate solvent, where the
fluoroelastomer comprises from about 5 to about 95 weight percent
of the elastomer solids content of the solution; adding a
nucleophilic dehydrofluorinating agent selected from the group
consisting of aminosilanes and hydrocarbon diamines; and mixing the
resulting solution until the polymers have a crosslink density
value of at least about 1.times.10.sup.-4 mole of chains/cc as
measured by the Flory-Rehner equation.
2. The process of claim 1 where the chlorofluoroelastomer comprises
a copolymer or terpolymer of vinylidene fluoride,
chlorotrifluoroehtylene and from about 1 to about 40 mole percent
of a monomer selected from the group consisting of
hexafluoropropylene and tetrafluoropropylene.
3. The process of claim 1 where the nucleophilic
dehydrofluorinating agent is an aminosilane.
4. The process of claim 1 where the nucleophilic
dehydrofluorinating agent is an functional polyorganosiloxane.
5. The process of claim 1 where the fluoroelastomer comprises at
least about 50 weight percent of the elastomer solids content of
the solution.
6. The process of claim 1 wherein the composition is cured.
7. The product of the process of claim 1.
8. A process for fabricating a fuser member having an outer
elastomeric coating comprising applying a coating of the product of
the process of claim 1 to the fuser member and curing the
elastomeric coating.
9. A fuser system member comprising a supporting substrate and an
outer surface layer of the cured product of the process of claim
1.
10. The fuser system member of claim 9 wherein the supporting
substrate is a fuser roll, a pressure roll or a release agent donor
roll.
11. The fuser system member of claim 9 wherein the supporting
substrate is a cylindrical sleeve, a drum or a belt.
12. The fuser system member of claim 9 wherein said outer surface
layer has a thickness of about 10 to 250 micrometers.
13. A elastomer composition comprising a blend of a] a
fluoroelastomer comprising a terpolymer of vinylidene fluoride,
tetrafluoroethylene and hexafluoropropylene; and b] a
chlorofluoroelastomer comprising a copolymer or terpolymer of
vinylidene fluoride, chlorotrifluoroehtylene and from 0 to about 40
mole percent of a monomer selected from the group consisting of
hexafluoropropylene and tetrafluoropropylene; where the
fluoroelastomer comprises from about 5 to about 95 weight percent
of the elastomer solids content of the solution; and the polymers
have a crosslink density value of at least about 1.times.10.sup.-4
mole of chains/cm3 as measured by the Flory-Rehner equation.
14. The elastomer composition. of claim 13 where the
chlorofluoroelastomer comprises a copolymer or terpolymer of
vinylidene fluoride, chlorotrifluoroethylene and from about 1 to
about 40 mole percent of a monomer selected from the group
consisting of hexafluoropropylene and tetrafluoropropylene.
15. The elastomer composition of claim 13 further including a
filler material.
16. The elastomer composition of claim 8 wherein said filler is
treated with a silane coupling agent.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation-in-part of application
Ser. No. 09/772,576, filed Jan. 30, 2001.
BACKGROUND OF THE DISCLOSED EMBODIMENT(S)
[0002] 1. Field
[0003] The disclosed embodiments relate to blends of chloro/fluoro
curable elastomers and their use as release layer coatings for
fuser members and transport belts in electrostatographic printing
apparati.
[0004] 2. Brief Description of Related Developments
[0005] In a typical electrostatographic reproducing apparatus, a
light image of an original to be copied is recorded in the form of
an electrostatic latent image upon a photosensitive member and the
latent image is subsequently rendered visible by the application of
electroscopic thermoplastic resin and pigment particles which are
commonly referred to as toner. The visible toner image is then in a
loose powdered form and can be easily disturbed or destroyed. The
toner image is usually fixed or fused upon a support which may be
the photosensitive member itself or other support sheet such as
plain paper.
[0006] The use of thermal energy for fixing toner images onto a
support member is well known. To fuse electroscopic toner material
onto a support surface permanently by heat, it is usually necessary
to elevate the temperature of the toner material to a point at
which the constituents of the toner material coalesce and become
tacky. This heating causes the toner to flow to some extent into
the fibers or pores of the support member. Thereafter, as the toner
material cools, solidification of the toner causes the toner to be
firmly bonded to the support.
[0007] Typically, the thermoplastic resin particles are fused to
the substrate by heating to a temperature of between about
90.degree. C. to about 200.degree. C. or higher depending upon the
softening range of the particular resin used in the toner. It is
undesirable, however, to increase the temperature of the substrate
substantially higher than about 250.degree. C. because of the
tendency of the substrate to discolor at such elevated
temperatures, particularly when the substrate is paper.
[0008] Several approaches to thermal fusing of electroscopic toner
images have been described. These methods include providing the
application of heat and pressure substantially concurrently by
various means, such as a roll pair maintained in pressure contact,
a belt member in pressure contact which a roll, and the like. Heat
may be applied by heating one or both of the rolls, plate members
or belt members. The fusing of the toner particles takes place when
the proper combination of heat, pressure and contact time is
provided. The balancing of these parameters to bring about the
fusing of the toner particles is well known in the art, and can be
adjusted to suit particular machines or process conditions.
[0009] During operation of a fusing system in which heat is applied
to cause thermal fusing of the toner particles onto a support, both
the toner image and the support are passed through a nip formed
between the roll pair or plate or belt members. The concurrent
transfer of heat and the application of pressure in the nip affect
the fusing of the toner image onto the support. It is important in
the fusing process that no offset of the toner particles from the
support to the fuser member take place during normal operations.
Toner particles that offset onto the fuser member may subsequently
transfer to other parts of the machine or onto the support in
subsequent copying cycles, thus increasing the background or
interfering with the material being copied there. The referred to
"hot offset" occurs when the temperature of the toner is increased
to a point where the toner particles liquefy and a splitting of the
molten toner takes place during the fusing operation with a portion
remaining on the fuser member. The hot offset temperature or
degradation of the hot offset temperature is a measure of the
release property of the fuser roll, and accordingly it is desired
to provide a fusing surface which has a low surface energy to
provide the necessary release. To ensure and maintain good release
properties of the fuser roll, it has become customary to apply
release agents to the fuser roll during the fusing operation.
Typically, these materials are applied as thin films of, for
example, silicone oils to prevent toner offset.
[0010] Fusing systems using fluoroelastomers as surfaces for fuser
members are described in U.S. Pat. No. 4,264,181 to Lentz et al.,
U.S. Pat. No. 4,257,699 to Lentz, and U.S. Pat. No. 4,272,179 to
Seanor, all commonly assigned to the assignee of the disclosed
embodiments. The disclosure of each of these patents is hereby
incorporated by reference herein in their entirety.
[0011] U.S. Pat. No. 5,017,432 describes a fusing surface layer
obtained from a specific fluoroelastomer, poly
(vinylidenefluoride-hexafluoropropy- lene-tetrafluoroethylene)
where the vinylidenefluoride is present in an amount of less than
40 weight percent. This patent further discloses curing the
fluoroelastomer with VITON.RTM. Curative No. 50 (VC-50) available
from E. I. Du Pont de Nemours, Inc., which is soluble in a solvent
solution of the polymer at low base levels and is readily available
at the reactive sites for crosslinking. This patent also discloses
use of a metal oxide (such as cupric oxide) in addition to VC-50
for curing.
[0012] U.S. Pat. No. 5,061,965 to Ferguson et al. the disclosure of
which is hereby incorporated by reference in its entirety,
discloses an elastomer release agent donor layer comprising
poly(vinylidenefluoride-he- xafluoropropylene-tetrafluoroethylene)
where the vinylidenefluoride is present in an amount less than 40
weight percent and a metal oxide. The release agent donor layer is
cured with a nucleophilic curing agent in the present of an
inorganic base.
[0013] Tan et al., U.S. Pat. No. 5,935,712, dated Aug. 10, 1999 and
entitled Fuser member with Surface Treated SnO2, CuO, or Mixture
Filler discloses a fuser member having improved toner offset
release and wear characteristics where the outermost layer
comprises a fluoroelastomer with thermally conductive fillers which
are surface treated with a coupling agent that is interactive with
the fluoroelastomer and with a release agent which may, optionally,
be used on the surface of the fluoroelastomer layer.
[0014] Caporiccio et al., U.S. Pat. No. 4,612,351 dated Sep. 16,
1986 and entitled Fluoroelastomeric Compositions Based on
Vinylidene Fluoride, Containing Small Amounts of
Chlorotrifluoroethylene, Having a High Adhesion to Metals in the
Vulcanized State, discloses fluoroelastomeric compositions based on
vinylidene fluoride, having a high adhesion to metals in the
vulcanized state, and characterized in that they contain small
amounts of chlorotrifluoroethylene which is present as a comonomer
of an elastomeric copolymer of vinylidene fluoride.
[0015] Kolb, U.S. Pat. No. 3,884,877, dated May 20, 1975, and
entitled Fluoroelastomer Compositions with Triorganophosphorus
Oxide discloses a curable vinylidene fluoride elastomer formulation
including triorgano phosphoirus oxide to provide desirable curing
characteristics.
[0016] Generally, the process for providing the elastomer surface
on the fusing system member, e.g., donor roll, pressure roll, fuser
roll, toner transfer belt or roller surfaces, and the like,
includes forming a solvent solution/dispersion by mixing a
fluoroelastomer dissolved in a solvent such a methyl ethyl ketone
and methyl isobutyl ketone, a dehydrofluorinating agent such as a
base, for example the basic metal oxides. MgO and/or Ca(OH).sub.2,
and a nucleophilic curing agent such as VC-50 which incorporates an
accelerator and a crosslinking agent, and coating the solvent
solution/dispersion onto the substrate. The surface is then
stepwise heat cured. Prior to the stepwise heat curing, ball
milling is usually performed, for from 2 to 24 hours.
[0017] While these and other fluoroelastomers have proven
satisfactory as fuser release surfaces, it is desirable to provide
elastomeric materials having even lower surface energy wherein
release properties are further enhanced. It is also desirable to
provide elastomers as fuser release surfaces possessing improved
physical properties, enhanced wear resistance and reduced chemical
reactivity with toner resins and additives, paper fibers and other
potential contaminants within the fusing subsystem.
SUMMARY
[0018] The disclosed embodiments provide an elastomer composition
comprising a blend of a fluoroelastomer comprising a terpolymer of
vinylidene fluoride, tetrafluoroethylene and hexafluoropropylene
and a chlorofluoroelastomer comprising a copolymer or terpolymer of
vinylidene fluoride, chlorotrifluoroethylene and 0 to about 40 mole
percent of one monomer selected from hexafluoropropylene and
tetrafluoroethylene; said fluoroelastomer present in said
composition at a level of from about 5 to 95% by weight of the
elastomer content of said composition.
[0019] Surprisingly, the compositions of the disclosed embodiments,
although utilizing art recognized components, provide superior
characteristics due to the high degree of cross linking in the
inventive compositions caused by the unique compounding method
utilized in obtaining the compositions.
[0020] In prior art processes utilizing silanes, the silane and
oxide fillers are mixed in solution phase and then dried prior to
dry compounding with the desired polymers.
[0021] In the novel process of the disclosed embodiments, the
silane is combined with a mixture of polymers in solution phase to
crosslink the polymers.
[0022] Surprisingly we have found that this preparation process
co-vulcanizes the plastic component with the elastomeric component
and yields a two phase composite material. In this process the
aminosilane, through nucleophilic attack, creates unsaturation in
the polymer backbone of the elastomer and plastic after which the
aminosilane undergoes oligimerization with subsequent crosslinking
of the two unsaturated polymer chains. A crosslink density value of
approximately 1.times.10.sup.-4 is obtained which in turn provides
a notable increase in toughness and initial modulus.
[0023] Suitable crosslinkers for the disclosed compositions include
aminosilanes and hydrocarbon diamines. Aminosilane crosslinkers are
the preferred crosslinkers and the aminosilanes disclosed in U.S.
Pat. No. 5,366,772, the disclosure of which is incorporated herein
and made a part hereof, are especially preferred.
[0024] The disclosed embodiments also provide a fuser system member
used in electrostatographic printing applications wherein a
supporting substrate such as a fuser roll or belt contains an outer
release layer comprising the cured elastomer composition of the
disclosed embodiments.
[0025] The cured composition provides for a lower surface energy
coating having enhanced toner release properties thereby reducing
the tendency for toner to offset back to the surface of the fuser
member during the electrostatographic printing process. The cured
composition also exhibits improved wear and physical properties
over similar fluoroelastomer compositions currently used in fusing
applications.
BRIEF DESCRIPTION OF THE DRAWINGS
[0026] FIG. 1 is a microphotograph of the structure of a disclosed
composition showing well defined domains in the composite
structure.
[0027] FIG. 2 shows the change in properties as the ration of
components of the composition is changed.
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0028] Suitable fluoroelastomers which provide the
fluoroelastomeric component of the disclosed embodiments are
perfluororubbers of the polymethylene type having all substituent
groups on the polymer chain either fluoro, perfluoroalkyl or
perfluoroalkoxy groups, and wherein the polymer is free of other
halogen substituents such as chlorine groups.
[0029] The fluoroelastomers useful in the practice of the disclosed
embodiments are those described in detail in U.S. Pat. No.
4,257,699 to Lentz, as well as those described in commonly assigned
U.S. Pat. Nos. 5,017,432 to Eddy et al. and 5,061,965 to Ferguson
et al. As described therein, these fluoroelastomers, particularly
from the class of copolymers, terpolymers, and tetrapolymers of
vinylidenefluoride, hexafluoropropylene, tetra-fluoroethylene, and
cure site monomer (believed to contain bromine) are known
commercially under various designations such as Viton A, Viton
E60C, Viton E430, Viton 910, Viton GH, Viton GF and Viton F601C.
The Viton designation is a Trademark of E. I. Dupont deNemours,
Inc. Other commercially available materials include Fluorol 2170,
Fluorol 2174, Fluorol 2176, Fluorol 2177 and Fluorol LVS 76,
Fluorol being a Trademark of 3M Company. Additional commercially
available materials include Aflas
poly(propylene-tetrafluoroethylene) copolymer, Fluorel II, a
poly(propylene-tetrafluoroethylene-vinylideneflu- oride) terpolymer
both also available from 3M Company. Typically, these
fluoroelastomers can be cured with a nucleophilic additive curing
system, such as a bisphenol crosslinking agent with an
organophosphonium salt accelerator as described in further detail
in the above referenced Lentz Patent and in the Eddy et al. patent
or with a peroxide in which case a cure site monomer such as
bromomethyl perfluorovinyl ether is also necessary.
[0030] A particularly preferred embodiment of the
hydrofluoroelastomer is that described in U.S. Pat. No. 5,017,432
to Eddy et al. which provides a fuser member surface layer
comprising polyvinylidenofluoride-hexafluoropr-
opylene-tetrafluoroethylene-cure site monomer (believed to contain
bromine) wherein the vinylidenefluoride is present in an amount
less than 40 weight percent and which is cured from a dried solvent
solution thereof with a nucleeophilic curing agent soluble in the
solvent solution and in the presence of less than 4 parts by weight
inorganic base per 100 parts of polymer, the inorganic base being
effective to at least partially dehydrofluorinate the
vinylidenefluoride. These materials are described in greater detail
in U.S. Pat. No. 5,017,432. The nucleophillic curing system is
further described in greater detail in U.S. Pat. No. 4,272,179 to
Seanor and U.S. Pat. No. 4,264,101 to Lentz et al.
[0031] The chlorofluoro elastomers which provide the
chlorofluoroelastomeric component of the disclosed embodiments
include co-and terpolymers comprising vinylidene fluoride,
chlorotrifluoroethylene and from 0 to about 40, preferably from
about 1 to about 40 mole percent, of at least one monomer selected
from hexafluoropropylene and tetrafluoroethylene. These are
analogous to the fluoroelastomers described above except that they
contain some chloro substituent groups which tend to enhance the
solubility of these polymers in organic solvent and further
facilitate co-crosslinking with the fluoroelastomer component of
the blend. Suitable chlorofluoroelastomers include copolymers of
vinylidene fluoride with chlorotrifluoroethylene and terpolymers
comprising the above two monomers with up to 40 mole percent of
hexafluoropropylene or tetrafluoroethylene. Preferred copolymers
contain from about 20 to 40 mole % vinylidene fluoride and
correspondingly from about 60 to 80 mole % chlorotrifluoroethylene;
preferred terpolymers contain from about 15 to 25 mole % vinylidene
fluoride from about 35 to 84 mole % chlorotrifluoroethylene and
from about 1 up to 40 mole % of either hexafluoropropylene or
tetrafluoroethylene.
[0032] Chlorofluoroelastomers particularly suitable for use in the
disclosed embodiments are more specifically described in U.S. Pat.
Nos. 3,988,502 and 4,032,699, the complete disclosure of which
patents are incorporated herein by reference.
[0033] These elastomers may be blended in a ratio such that either
elastomer comprises from about 5 to 95 wt % of the elastomeric
content of the composition. Preferably the fluoroelastomer will
constitute at least 50 wt % of the elastomer content of the
composition.
[0034] The fluoro and chlorofluoro elastomer blend may be cocured
(covulcanized) using any of the nucleophilic, free radical or amine
curing systems which are well known in the art for curing
fluoroelastomers. Nucleophilic curing systems may include a
bispehnol crosslinking agent and an organophosphonium salt
accelerator. Typically, the curing process takes place in the
presence of 8 to 10 parts by weight of inorganic base per 100 parts
of polymer. The inorganic base dehydrofluorinates the
vinylideneflouride in the polymer, creating double bonds which act
as reactive sites for crosslinking. However, the presence of excess
base results in the long term degradation of the elastomers and if
excess base continues to dehydrofluorinate the vinylidenefluoride
generating double bonds which cause the toner member to harden,
subsequent oxidation causes the surface energy to increase and the
release performance to degrade. Thus, it is preferred to cure the
polymer at a relatively low base level to control the reactivity of
the vinylidenefluoride.
[0035] A typical nucleophilic curing system is disclosed in U.S.
Pat. No. 4,272,179, the complete disclosure of which is
incorporated herein by reference.
[0036] Other curatives which can be employed include peroxides,
hydrides, bases, oxides, amines and the like. Examples of strong
nucleophilic agents include primary, secondary and tertiary
aliphatic and aromatic amines, as well as amino silanes such as
disclosed in U.S. Pat. Nos. 5,700,568 and 5,729,813, the complete
disclosure of which patents are incorporated herein by
reference.
[0037] Other adjuvants and fillers may be incorporated in the
elastomer composition in accordance with the disclosed embodiments
provided that they do not adversely effect the integrity of the
fluoroelastomer. Such fillers normally encountered in the
compounding of elastomers include coloring agents, reinforcing
fillers such as carbon black and silica, and processing aids. Also:
Aluminum oxide, indium tin oxide, antimony tin oxide, silicon
carbide, zinc oxide and boron nitride may be included as fillers,
which may be present at a level of from about 1-20 volume percent.
Oxides such as copper oxides may be added in certain amounts such
as, for example, from about 1 to about 10 volume percent, to fuser
roll coatings to provide sufficient anchoring sites for functional
release oils and thereby allow excellent toner release
characteristics from such members. Fillers may optionally be
pre-treated or treated in solution with silane coupling agents to
improve filler incorporation into the polymer network.
[0038] The substrate for the fuser member of the fuser system
assembly may be a roll, belt, flat surface or other suitable shape
used in the fixing of thermoplastic toner images to a suitable
substrate. It may take the form of a fuser member, a pressure
member or a release agent donor member, preferably in the form of a
cylindrical roll. Typically, the substrate takes the form of a
cylindrical tube of aluminum, copper, steel or certain plastic
materials chosen to maintain rigidity and structural integrity as
well as being capable of having the elastomer coated thereon and
adhered firmly thereto. The diameter of the substrate is from about
10 to about 100 mm, and preferably from about 40 to about 75 mm. It
is preferred that the supporting substrate is a cylindrical sleeve
having an outer layer of from about 1 to about 6 mm. In one
embodiment, the core, which may be a steel cylinder is degreased
with a solvent and cleansed with an abrasive cleaner prior to being
primed with a primer, such as Dow Corning 1200, which may be
sprayed, brushed or dipped, followed by air drying under ambient
conditions for thirty minutes and then baked at 150.degree. C. for
30 minutes.
[0039] The outer layer of the fuser member is preferably prepared
by dissolving the elastomer in a typical solvent such as methyl
ethyl ketone, methyl isobutyl ketone and the like. A nucleophilic
dehydrofluorinating agent is then added followed by stirring for 1
to 60 minutes at 45.degree. to 85.degree. C. The resulting solution
is then used to fabricate the outer layer of a fuser member by
conventional solution coating methods, spraying, dipping, flow
coating, or the like. The coating thickness can vary depending upon
specific applications from about 10 to about 250 micrometers thick.
The coating is first air dried and then step heat cured is in air.
For fuser applications, the thickness of the dry fluroelastomer
layer could be any suitable thickness, for example, from 25 to
about 75 and preferably from about 35 to about 50 micrometers. This
thickness range is selected to provide a layer thin enough to
prevent a large thermal barrier for fusing and thickness enough to
allow a reasonable wear life. While molding, extruding and wrapping
techniques are alternative means which may be used, it is preferred
to spray or flow-coat successive applications of the solvent
solution. When the desired thickness of coating is obtained, the
coating is cured and thereby bonded to the roll surface.
[0040] The curing time, is for example, from about 30 minutes to
about 24 hours and the preferred time is from about 1 to 4 hours,
and particularly preferred is from about 1 to about 2 hours. The
temperature for curing is from about 100.degree. to about
150.degree. C., and preferably from about 130.degree. to about
150.degree. C.
[0041] The following example is illustrative of the disclosed
embodiments. As used in the example, FK-800 is a copolymer of
chlorotrifluoroethylene and vinylidene fluoride containing about 74
wt % chlorotrifluoroethylene (available from 3M or Mach 1, Inc.
King of Prussia, Pa.) and Viton GF is a terpolymer of 35 wt %
vinylidene fluoride, 34 wt % hexafluoropropylene and 29 wt %
tetrafluoroethylene available from Dupont.
EXAMPLE 1
[0042] Several 20% solids solution comprising varying weight
percentages of FK-800 and Viton GF in methyl isobutyl ketone was
prepared. An appropriate amount of an aminosilane,
aminoethyl-aminopropyl trimethoxysilane (AO700, available from
United Chemical Technologies), was added to each solution to
provide a cured composition possessing a similar crosslink density
value, i.e. approximately 1.times.10.sup.-4 moles of chains per
cubic centimeter as measured by the Flory-Rehner equation. This
solution along with identical control solutions containing only
Viton GF as the elastomer components were placed in a small glass
dish and allowed to desolvate. The resulting films were then soaked
overnight in methylethyl ketone with no apparent solubilizing which
indicated a crosslinked matrix. The Test films were submitted for
physical properties. Data and more information on the compositions
is in Table 1.
1TABLE 1 Table of Tested Films, Properties Composition I.D. 2 3 4 5
6 Wt. Percent FK-800 85 70 55 0 0 Wt. Percent Viton GF 15 30 45 100
100 AO700, pph 7 8 9 5 8 Tensile Strength, PSI 1325 1704 1572 1265
1627 Elongation, % 242 308 204 382 223 Toughness, in-lb/in.sup.3
1707 2954 2094 2004 1678 Initial Modulus, PSI 1479 2183 3847 630
1498 Release Strength, oz./in- 12.9 11.8 9.1 18.3 17.3 Abrasion
Resistance, 77.5 73.3 NT (not 59.2 50.3 mg. loss/500 cycles tested)
Mol % Vinylidene 29.6 33.2 36.8 50.0 50.0 Fluoride Mol % 3.0 6.0
9.0 20.0 20.0 Hexafluoropropylene Mol % 4.5 9.0 13.5 30.0 30.0
Tetrafluoroethylene Mol % 62.9 51.8 40.7 0.0 0.0
Chlorotrifluoroethylene Wt % Vinylidene 18.9 21.7 24.6 35.0 35.0
Fluoride Wt % 5.0 9.9 14.9 33.0 33.0 Hexafluoropropylene Wt % 4.8
9.6 14.4 32.0 32.0 Tetrafluoroethylene Wt % 71.4 58.8 46.2 0.0 0.0
Chlorotrifluoroethylene
[0043] Compositions ID 2-4 are the inventive compositions;
Compositions ID 5 and 6 are prior art compositions. Composition ID
5 is an example of the prior art, demonstrating the properties
obtained without co-vulcanization of the plastic. Composition ID 6
in comparison with Composition ID 3 demonstrates the improvement in
properties when the inventive compositions are utilized. The weight
and mol % are indicative of the starting compositions, not of the
final composition of the amino-silane crosslinker portion of the
final crosslinked polymer network.
[0044] FIG. 1 illustrates the structure of the inventive
compositions. FIG. 2 shows the characteristics at different
percentages of the components of the compositions.
[0045] It should be noted that the physical properties are more
plastic-like with addition of FK-800, as the initial modulus
increased. The other properties important for fusing materials
increase as well, while maintaining a comparable elongation
(percent strain at break) as compared to the control material,
Viton GF 100%.
[0046] While particular embodiments have been described, various
alternatives, modifications, variations, improvements, and
substantial equivalents that are or may be presently unforeseen may
arise to Applicant's or others skilled in the in the art.
Accordingly, the appended claims as filed, and as they may be
amended, are intended to embrace all such alternatives,
modifications, variations, improvements and substantial
equivalents.
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