U.S. patent application number 16/095520 was filed with the patent office on 2019-05-02 for spray application systems components comprising a repellent surface comprising a siloxane material & methods.
The applicant listed for this patent is 3M INNOVATIVE PROPERTIES COMPANY. Invention is credited to Cheryl L. S. Elsbernd, Jeffrey O. Emslander, Kent C. Hackbarth, David S. Hays, Phillip H. Henna, Stephen C. P. Joseph, David J. Kinning, Adam J. Meuler, Jon P. Nietfeld, Nicholas L. Untiedt, Elaine M. Yorkgitis.
Application Number | 20190126301 16/095520 |
Document ID | / |
Family ID | 58631056 |
Filed Date | 2019-05-02 |
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United States Patent
Application |
20190126301 |
Kind Code |
A1 |
Meuler; Adam J. ; et
al. |
May 2, 2019 |
SPRAY APPLICATION SYSTEMS COMPONENTS COMPRISING A REPELLENT SURFACE
COMPRISING A SILOXANE MATERIAL & METHODS
Abstract
Presently described are components of a spray application
system. At least one component comprises a liquid repellent surface
layer. The liquid repellent surface (e.g. layer) comprises a
siloxane material. The component is typically a liquid reservoir, a
liquid reservoir liner, a lid for a liquid reservoir or liner, or a
combination thereof. In some embodiments, the component comprises a
thermoplastic polymeric material. In some favored embodiments, the
component is a removable liquid reservoir or liner. In some favored
embodiments, the component is a collapsible liquid reservoir or
liner. The spray application system typically further comprises a
gravity-fed spray gun. Also described are spray application
systems, methods of using a spray application system, as well as
methods of making a component of a spray application system wherein
the component has a liquid repellent surface.
Inventors: |
Meuler; Adam J.; (Woodbury,
MN) ; Yorkgitis; Elaine M.; (St. Paul, MN) ;
Hays; David S.; (Woodbury, MN) ; Hackbarth; Kent
C.; (River Falls, WI) ; Joseph; Stephen C. P.;
(Woodbury, MN) ; Elsbernd; Cheryl L. S.;
(Woodbury, MN) ; Nietfeld; Jon P.; (Woodbury,
MN) ; Henna; Phillip H.; (Cottage Grove, MN) ;
Kinning; David J.; (Woodbury, MN) ; Untiedt; Nicholas
L.; (Minneapolis, MN) ; Emslander; Jeffrey O.;
(Grant, MN) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
3M INNOVATIVE PROPERTIES COMPANY |
St. Paul |
MN |
US |
|
|
Family ID: |
58631056 |
Appl. No.: |
16/095520 |
Filed: |
April 26, 2017 |
PCT Filed: |
April 26, 2017 |
PCT NO: |
PCT/US17/29573 |
371 Date: |
October 22, 2018 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
62327783 |
Apr 26, 2016 |
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
B05B 7/2481 20130101;
C08K 5/5415 20130101; B05B 7/2478 20130101; B05B 7/2408 20130101;
B05D 5/083 20130101; C09D 201/04 20130101; C08K 5/02 20130101; C09D
167/02 20130101 |
International
Class: |
B05B 7/24 20060101
B05B007/24 |
Foreign Application Data
Date |
Code |
Application Number |
Oct 21, 2016 |
US |
PCT/US2016/058166 |
Claims
1. A component of a spray application system, the component
comprising a liquid repellent surface such that the receding
contact angle with a solution containing 10% by weight of
2-n-butoxyethanol and 90% by weight deionized water is at least 35
degrees; wherein the liquid repellent surface comprises a surface
layer comprising a silane or siloxane material and liquid repellent
surface is not a lubricant impregnated surface.
2. The component of claim 1 wherein the liquid repellent surface
comprises a solid liquid repellent material.
3. The component of claim 1 wherein the siloxane material comprises
at least 50 wt.-% polydimethylsiloxane.
4. The component of claim 1 wherein the siloxane material comprises
a siloxane backbone and hydrocarbon side chains averaging at least
8 carbon atoms and no greater than 50 carbon atoms.
5. The component of claim 1 wherein the siloxane material
comprising polydimethylsiloxane does not comprise vinyl groups or
other groups that form a crosslinked network.
6. (canceled)
7. The component of claim 1 wherein the siloxane material has a
viscosity at 25.degree. C. of 5,000,000 or 10,000,000
centistokes.
8. (canceled)
9. The component of claim 1 wherein the siloxane material is a
copolymer comprising less than 50 wt.-% polydimethylsiloxane.
10. The component of claim 9 wherein the siloxane material is
copolymer of polyorganosiloxane and polyolefin or
polycarbonate.
11. The component of claim 1 wherein the liquid repellent surface
is liquid repellent after 2 abrasion cycles at 15 cycles/minute
with a Taber Linear Abraser.
12. The component of claim 1 wherein the component is a liquid
reservoir, a liquid reservoir liner, a lid for a liquid reservoir
or liner, or a combination thereof.
13. The component of claim 12 wherein the component comprises a
thermoplastic polymeric material.
14. The component of claim 12 wherein the component is a removable
liquid reservoir liner.
15. (canceled)
16. The component of claim 12 wherein the spray application system
further comprises a gravity-fed spray gun.
17. The component of claim 1 wherein the liquid repellent surface
layer repels water-based paint having a volatile organic solvent of
at least 5, 10, 15, 20, or 25 g/liter; wherein the volatile organic
solvent is water-soluble.
18. (canceled)
19. The component of claim 17 wherein the organic solvent comprises
one or more alcohol.
20. (canceled)
21. The component of claim 17 wherein the organic solvent comprises
2-butoxyethanol, butoxypropan-2-ol, 2-(2-butoxyethoxy)ethanol, and
mixtures thereof.
22. The component of claim 1 wherein the liquid repellent surface
is liquid repellent such that retained paint has a mass no greater
than 0.01 g/cm.sup.2 or a drop of paint slides off the liquid
repellent surface when oriented vertically.
23. (canceled)
24. The component of claim 1 wherein the liquid repellent surface
has a receding contact angle with water from 90 degrees to 135
degrees.
25. (canceled)
26. A component of a spray application system, the component
comprising a liquid repellent surface such that the mass of
retained test liquid is no greater than 0.01 g/cm.sup.2 when the
test liquid is selected from 400 Mw polypropylene glycol,
butoxythanol, or a 50 wt. % aqueous solution of butoxyethanol;
wherein the liquid repellent surface comprises a surface layer
comprising a silane or siloxane material and the liquid repellent
surface is not a lubricant impregnated surface.
27. (canceled)
28. A spray application system comprising a spray gun, a liquid
reservoir that attaches to the spray gun, optionally a liner for
the liquid reservoir, a lid for the liquid reservoir and/or liner;
wherein at least the liquid reservoir and/or liner comprising a
liquid repellent surface layer as described in claim 1.
Description
BACKGROUND
[0001] As described for example in WO98/32539, spray application
systems for spraying liquids (e.g. paints, garden chemicals etc.)
are generally known. Such systems generally comprise a reservoir to
contain a liquid and a spray gun through which the liquid is
dispensed. The liquid may be fed from the reservoir under gravity
and/or it may be entrained in a stream of pressurized liquid, for
example air or water, which is supplied to the gun from an external
source.
[0002] As also described in WO98/32539 disposable liners have been
used with (e.g. re-usable) liquid reservoirs. The liner may aid in
disposal of the contents; protect the reservoir or its contents; as
well as facilitate or even eliminate the cleaning of the
reservoir.
SUMMARY
[0003] With current spray (e.g. paint) application systems, a
portion of the liquid (e.g. paint) is retained within the liquid
reservoir or liner after dispensing the liquid. Depending on the
size of the liquid reservoir or liner, the amount of retained paint
may range from about 1/2 to 1 ounce. In the case of relatively
expensive liquids, such as colored automobile base coat paints that
can cost $3-$6 per sprayable ounce, the cost of such wasted
retained (e.g. paint) liquid can be substantial. Thus, industry
would find advantage in minimizing the amount of paint or other
liquid that is retained on components of spray application
systems.
[0004] One commonly known class of fluoropolymer is Teflon.TM. PTFE
resin or in other words polytetrafluoroethylene polymers prepared
by the polymerization of the monomer tetrafluoroethylene ("TFE"
having the structure CF.sub.2.dbd.CF.sub.2). Teflon.TM. PTFE resins
are described as crystalline materials. Crystalline PTFE resins
typically have a density of about 2.2 g/cm.sup.3.
[0005] It has been found that Teflon.TM. PTFE does not provide a
liquid repellent surface such that the receding contact angle with
water is at least 90 degrees and/or the difference between the
advancing contact angle and the receding contact angle of the
surface with water is less than 10. Further, Teflon.TM. PTFE also
does not provide an (e.g. aqueous) paint repellent surface as
determined by test methods set forth in the examples.
[0006] Presently described are components of a spray application
system. At least one component comprises a liquid repellent surface
(e.g. layer). In some embodiments, the liquid repellent surface
comprises a silane or siloxane (e.g. polydimethylsiloxane)
material, wherein the liquid repellent surface is not a lubricant
impregnated surface. In some embodiments, the liquid repellent
surface comprises a (e.g. layer of) thermally processible polymer
and a siloxane melt additive. The component is typically a liquid
reservoir, a liquid reservoir liner, a lid for a liquid reservoir
or liner, or a combination thereof. In some embodiments, the
component comprises a thermoplastic polymeric material. In some
favored embodiments, the component is a removable liquid reservoir
or liner. In some favored embodiments, the component is a
collapsible liquid reservoir or liner. The spray application system
typically further comprises a gravity-fed spray gun.
[0007] Also described are spray application systems, methods of
using a spray application system, as well as methods of making a
component of a spray application system wherein the component has a
liquid repellent surface.
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] FIG. 1 is a perspective view of a spray application
system;
[0009] FIG. 2 shows an exploded view of components of a liquid
(e.g. paint) reservoir further comprising a liner for the gun of
FIG. 1;
[0010] FIG. 3 shows the liquid reservoir of FIG. 2 in an assembled
condition, with an adapter 21 for connecting the liquid reservoir
to a spray gun;
[0011] FIG. 4 shows a longitudinal cross-section through the liquid
reservoir and the adapter of FIG. 3;
[0012] FIG. 5 shows the collapsed liner after the liquid (e.g.
paint) has been dispensed from a reservoir or liner;
[0013] FIG. 6 is cross-sectional view of another embodiment of an
article comprising a liquid repellent surface;
[0014] FIG. 7 is cross-sectional view of another embodiment of an
article comprising a liquid repellent surface;
[0015] FIG. 8 is cross-sectional view of another embodiment of an
article comprising a liquid repellent surface; and
[0016] FIG. 9 is cross-sectional view of another embodiment of an
article comprising a liquid repellent surface. The cross-sectional
drawings are not to scale.
DETAILED DESCRIPTION
[0017] FIG. 1 illustrates an embodied spray application system. The
gun 1 comprises a body 2, a handle 3 which extends downwards from
the rear end of the body, and a spray nozzle 4 at the front end of
the body. The gun is manually-operated by a trigger 5 which is
pivotally-mounted on the sides of the gun. The liquid (e.g. paint)
reservoir 6 is located on the top of the body 2 and communicates
with an internal (e.g. air) passageway (not visible) which extends
through the gun from a connector 7 at the lower end of the handle 3
to the nozzle 4. During use, liquid (e.g. paint) is provided in
reservoir 6. Removable lid 8 is engaged with the open end of (e.g.
paint) liquid reservoir 6. Further, connector 7 is connected to a
source of compressed air (not shown) so that, when the user pulls
on the trigger 5, compressed air is delivered through the gun to
the nozzle 4 (or functionally similar assembly) and entrains and
atomizes paint being delivered under gravity from liquid reservoir
6. The liquid (e.g. paint) is then discharged through the nozzle 4
with the compressed air, as a spray.
[0018] Various spray gun designs can be utilized in the embodied
spray application system, such as described for example in U.S.
Pat. Nos. 5,582,350; 5,267,693; and EP 0768 921. In some
embodiments, the spray application system may further comprise
tubes or hoses, typically disposed between the (e.g. paint) liquid
reservoir and the gun.
[0019] FIG. 2 illustrates the components of another embodied liquid
(e.g. paint) reservoir 11 that can be used with the gun 1 of FIG. 1
(or any similar gun) instead of liquid (e.g. paint) reservoir 6.
The liquid (e.g. paint) reservoir 11 comprises an open container
12, of suitable size for attachment to a (e.g. hand-held) spray
gun, having an air hole 12A in its base and provided with a liner
13. The liner 13 corresponds in shape to and fits within the
interior of container 12. The (e.g. removable) liner may have a
narrow rim 14 at the open end that contacts the top edge of the
container 12. The container 12 also has a (e.g. disposable) lid 15.
Lid 15 typically engages rim 14 of the open end of the liner 13 and
is held firmly in place when lid 15 is attached to container 12.
The lid can be attached by an annular collar 20 which screws onto
the container, such as depicted in FIG. 3.
[0020] Liquid reservoir 6 or container 12 of the liquid (e.g.
paint) reservoir 11 is typically formed from a self-supporting
(e.g. rigid) thermoplastic polymeric material, for example
polyethylene or polypropylene, of any suitable size. For use with
paint spray guns, containers having a capacity ranging from 100 ml
to 1 liter, such as a capacity of 250, 500 or 800 ml, are common.
The lid 15 is also typically formed from a thermoplastic polymeric
material, for example, polyethylene or polypropylene. The lid may
be transparent, translucent or opaque and may optionally be
colored. The collar 20 may be a molded thermoplastic or it may be a
machined metal (for example, aluminum). In some embodiments, fluid
reservoir 6 and container 12 are formed by injection molding of a
thermoplastic polymer.
[0021] Liquid reservoir 6, as well as liner 13, are typically also
self-supporting but can also be collapsible, i.e. collapses when
(e.g. paint) liquid is withdrawn from the liner or liquid (e.g.
paint) reservoir during operation of the spray gun. In one
embodiment, the liner 13 or liquid (e.g. paint) reservoir 6 have a
(e.g. thicker) rigid base 13A and (e.g. thinner) flexible side
walls 13B. In this embodiment, the base may have a thickness of
about 250 to 400 microns. In contrast, the side walls can range
from about 100 to 250 microns and in some embodiments are no
greater than 225, 200 or 175 microns. When the liner collapses, it
typically collapses in the longitudinal (or axial) direction by
virtue of the side walls collapsing rather than the base. Liner 13
and some embodiments of liquid (e.g. paint) reservoir 6 are
preferably formed by thermo/vacuum forming a sheet of thermoplastic
material such as low density polyethylene (LDPE). When the liner 13
or liquid (e.g. paint) reservoir 6 is collapsible it can be
characterized as a single-use or in other words "disposable"
component.
[0022] The lid 15 typically includes a (e.g. central) aperture 16
from which extends a connector tube 17 provided, at its end, with
outward extensions 18 forming one part of a connection, such as a
bayonet connection; i.e. a fitting engaged by being pushed into a
socket and then twisted to lock in place. The liquid (e.g. paint)
reservoir 11 can be attached to the spray gun 1 through the use of
an adapter 21 as depicted in FIG. 3 and FIG. 4. The adapter 21 is a
tubular component which, at one end 22, is formed internally with
the other part of the (e.g. bayonet) connection for attachment to
the connector tube 17. The other end 23 of the adapter can be
shaped to match the standard attachment of the spray gun (typically
a screw thread). The adapter 21 may be a machined metal component
and may, for example, be formed from anodized aluminum or stainless
steel.
[0023] During use of the spray application system, adapter 21 is
securely attached (at end 23) to the spray gun. Liner 13 is
inserted into container 12. Liquid (e.g. paint) is then put into
liner 13, lid 15 is pushed into place, and collar 20 engaged (e.g.
screwed down) tightly with container 12 to hold the lid in
position. The rim 14 of the liner 13 is typically held in place
between lid 15 and container 12 as shown in FIG. 4. As paint is
removed from within the liner 13, the sides of the liner collapse
as depicted in FIG. 5 as a result of the decreased pressure within
the liner. The base of the liner, being more rigid, retains its
shape so that the liner tends to collapse in the longitudinal
rather than the transverse direction thereby reducing the
possibility of pockets of paint being trapped in the liner.
[0024] The liner 13 typically has a smooth (e.g. continuous)
internal surface, lacking structures that would increase retention
of the liquid (e.g. paint). Thus, the liner typically has no
discontinuities (projections or indentations) from a planar surface
such as pleats, corrugations, seams, joints, gussets, or groove(s)
at the internal junction of the side walls 13B with the base 13A.
Further, the liner volumetrically coincides with the inside of the
container 12.
[0025] Liquid (e.g. paint) can be mixed within liner 13 or within
liquid (e.g. paint) reservoir 6. To facilitate the use as a mixing
receptacle, the side walls of the container 12 or liquid (e.g.
paint) reservoir 6 may be provided with markings 25 (FIGS. 2 and 3)
enabling the volume of the contents within the container to be
determined.
[0026] Although fluid reservoir 6, container 12, and liner 13 may
be opaque, such components are preferably transparent or
translucent such that the liquid can be visually observed through
the walls. This can also facilitate using the fluid reservoir 6, or
container 12 and liner 13 as a measuring and mixing receptacle.
[0027] Liquid (e.g. paint) contained in the liquid reservoir 6 or
liner 13 is often mixed by hand. Hand mixing can be beneficial to
avoid air entrapment. The inside surfaces of the liquid reservoir 6
or liner 13 are also typically not exposed to high amounts of
mixing forces when mixed by hand. However, the side walls of the
mixing container may be `scraped` in order to ensure all of the
toners and other ingredients are thoroughly mixed.
[0028] In some embodiments, the liners are thermoformed, injection
molded, blow molded (or formed using some other plastic processing
technique) from materials such as, but not necessarily limited to,
low density polyethylene, polypropylene, polyethylene, and/or
blends thereof. Suitable liner components are commercially
available from 3M Company, St. Paul, Minn. under trade designation
"3M PPS PAINT PREPARATION SYSTEM".
[0029] To ensure that there are no unwanted particles, the liquid
(e.g. paint) typically passes through a (e.g. removable) filter as
the (e.g. paint) liquid passes from the liquid reservoir 6 or liner
13 to the spray gun or nozzle during use of the spray application
system. Such filter can be positioned at various locations. In one
embodiment, aperture 16 is covered by a filter mesh 19 which may be
a push fit into the aperture or may be an integral part of the lid
15, as depicted in FIG. 4. In another embodiment, a filter may be
provided within liquid reservoir 6, as described and depicted in
FIG. 12 of WO 98/32539.
[0030] FIGS. 1-9 depict examples of illustrative liquid (e.g.
paint) reservoirs, liquid reservoir liners, lids for liquid (e.g.
paint) reservoirs and liners. Such components may optionally
include various other adaptations as known in the art for spray
application systems, as described for examples in WO 98/32539.
[0031] In the present invention, a component (e.g. a liquid
reservoir, a liquid reservoir liner, a lid for a liquid reservoir
or liner, or a combination thereof) of a spray application system
comprises a liquid repellent surface (e.g. layer). The liquid
repellent surface layer may be present on a portion of a surface of
at least one of such components or the liquid repellent surface
layer may be present on the entire surface that comes in contact
with liquid (e.g. paint) during use. Although the exterior surfaces
of the liquid reservoir, liner, lid, etc. may comprise the liquid
repellent surface layer described herein, in typical embodiments,
the interior surface(s) of at least one of such components
comprises a liquid repellent surface layer.
[0032] When the liquid (e.g. paint) repellent surface comprises a
lubricant impregnated into pores of a porous layer as described in
WO2016/069674, the outer exposed surface is predominantly liquid
lubricant. Some structures of the porous layer may protrude through
the liquid lubricant and be present at the outer exposed surface.
However, the outer exposed surface is predominantly liquid
lubricant. In this embodiment, typically at least 50, 55, 60, 65,
70, 75, 80, 85, 90, 95% or greater of the surface area is a liquid
lubricant, as can be determined by microscopy. Thus, the aqueous
liquid (e.g. paint) that is being repelled comes in contact with
and is repelled by the liquid lubricant.
[0033] By "liquid" it is meant that the lubricant has a dynamic
(shear) viscosity of at least about 0.1, 0.5, or 1 mPa-s and no
greater than 10' mPa-s at the use temperature. In typical
embodiments, the dynamic viscosity is no greater than 10.sup.6,
10.sup.5, 10.sup.4, or 10.sup.3 mPa-s. The dynamic viscosity values
described herein refer to those measured at a shear rate of 1
sec.sup.-1.
[0034] In other embodiments as described herein, the liquid (e.g.
paint) repellent surface of the spray application system component
is not a lubricant impregnated surface. Rather the outer exposed
surface is predominantly a solid liquid (e.g. paint) repellent
material. In this embodiment, less than 50, 45, 40, 35, 30, 25, 20,
15, 10, 5, 4, 3, 2, 1, 0.5, 0.1, 0.005, or 0.001% of the surface
area is a liquid lubricant. Rather, at least 50, 55, 60, 65, 70,
75, 80, 85, 90, 95, 96, 97, 98, 99, or 99.5% or greater of the
outer exposed surface is a solid liquid-repellent material. Thus,
the aqueous liquid (e.g. paint) that is being repelled comes in
contact with and is repelled by the solid liquid-repellent
material.
[0035] The solid liquid (e.g. paint) repellent material is
generally a solid at the use temperature of the spray application
system component, which commonly ranges from 40.degree. F. to
120.degree. F. In typical embodiments, the solid liquid (e.g.
paint) repellent material is a solid at room temperature (e.g.
25.degree. C.). Thus, the solid liquid (e.g. paint) repellent
material has a melting temperature (peak endotherm as measured by
Differential Scanning calorimetry) greater than 25.degree. C., and
typically greater than 120.degree. F. (49.degree. C.). In some
embodiments, the solid liquid (e.g. paint) repellent material has a
melting temperature no greater than 200.degree. C. The solid (e.g.
paint) repellent material may exhibit more than one melting
temperature. In typical embodiments, a single solid liquid (e.g.
paint) repellent material is utilized. However, when the liquid
repellent surface is provided by a coating composition, the coating
composition may contain a mixture of solid liquid (e.g. paint)
repellent materials.
[0036] With reference to FIG. 6, article 200 is a component of a
spray application system comprising substrate or component 210
(e.g. a liner, liquid reservoir, or lid) comprising a liquid (e.g.
paint) repellent surface 253 that comprises a (e.g.
non-fluorinated) organic polymeric binder and a siloxane (e.g.
polydimethylsiloxane "PDMS") material. The concentration of
siloxane (e.g. PDMS) material at the outer exposed surface (e.g.
layer) 253 is typically higher than the concentration within the
(e.g. non-fluorinated) organic polymeric binder layer 251 proximate
substrate 210. In one embodiment, the liquid (e.g. paint) repellent
surface (e.g. layer) can be provided by coating substrate 210 with
a coating composition comprising an organic solvent, a (e.g.
non-fluorinated) organic polymeric binder, and a siloxane (e.g.
PDMS) material as will subsequently be described.
[0037] With reference to FIG. 7, article 300 is a component of a
spray application system comprising substrate or component 310
(e.g. a liner, liquid reservoir, or lid) comprising a liquid (e.g.
paint) repellent surface (e.g. layer) 353 that comprises a siloxane
(e.g. PDMS) material. The concentration of siloxane (e.g. PDMS)
material at the outer exposed surface (e.g. layer) 353 is typically
higher than the concentration of siloxane (e.g. PDMS) material
proximate the center of the substrate 310. In one embodiment, the
liquid (e.g. paint) repellent surface 353 can be provided by
including a siloxane (e.g. PDMS) material as a melt additive in a
polymeric material that is thermally processed to form substrate
310 into a component such as a liner, liquid reservoir, or lid.
[0038] With reference to FIG. 8, article 400 is a component of a
spray application system comprising substrate or component 410
(e.g. a liner, liquid reservoir, or lid) comprising a liquid (e.g.
paint) repellent surface 453 that comprises a siloxane (e.g. PDMS)
polymer layer, or a polymer comprising both fluorinated and silane
or siloxane groups 451. In one embodiment, the liquid (e.g. paint)
repellent surface 453 can be provided by coating substrate 410 with
a coating composition comprising an organic solvent and a siloxane
(e.g. PDMS) polymer, as will subsequently be described. The
siloxane content is typically the same throughout the thickness of
the siloxane layer. In another embodiment, the liquid (e.g. paint)
repellent surface 453 can be provided by coextruding substrate 410
together with a siloxane (e.g. PDMS) polymer layer 451 into a sheet
and thermally processing the sheet into a liner, liquid reservoir,
or lid.
[0039] With reference to FIG. 9, article 500 is a substrate or
component 510 of a spray application system such as a liner, liquid
reservoir, or lid, comprising a siloxane (e.g. PDMS) polymer. The
siloxane content is typically the same throughout the thickness of
the component. The interior and exterior surface of the component
typically comprise siloxane polymer. In another embodiment, the
liquid (e.g. paint) repellent surface can be provided by thermally
processing a siloxane polymer or a polymer comprising both
fluorinated and silane or siloxane groups into a component such as
a liner, liquid reservoir, or lid.
[0040] In other embodiments, the (e.g. paint) liquid repellent
surface comprises a siloxane (e.g. PDMS) material and a (e.g.
non-fluorinated) organic polymeric binder. In typical embodiments,
a major amount of non-fluorinated polymeric binder is combined with
a sufficient amount of siloxane (e.g. PDMS) material that provides
the desired repellency properties, as described herein.
[0041] In typical embodiments, the amount of siloxane (e.g. PDMS)
material is at least about 0.05, 0.1, 0.25, 0.5, 1.5, 2.0 or 2.5
wt.-% and in some embodiments, at least about 3.0, 3.5, 4.0, 4.5 or
5 wt.-%. The amount of siloxane (e.g. PDMS) material is typically
no greater than 50, 45, 40, 35, 30, 25, 20, 15, or 10 wt.-% of the
sum of the siloxane (e.g. PDMS) material and non-fluorinated
polymeric binder.
[0042] In other embodiments, the (e.g. paint) liquid repellent
surface comprises a siloxane (e.g. PDMS) material. In some
embodiments, the siloxane (e.g. PDMS) material is a solid rather
than a liquid (e.g. lubricant) at 25.degree. C. and at temperatures
ranging from 40.degree. F. (4.44.degree. C.) to 130.degree. F.
(54.4.degree. C.). In typical embodiments the siloxane (e.g. PDMS)
material is free of fluorinated groups and thus free of fluorine
atoms. However, in other embodiments, a predominantly siloxane
(e.g. PDMS) material may further comprise one or more fluorinated
groups. Although it is most common to utilize a siloxane (e.g.
PDMS) material, combinations of a fluorochemical material and a
siloxane (e.g. PDMS) material can be utilized.
[0043] In some embodiments, a major amount of non-fluorinated
polymeric binder or thermally processible polymer is combined with
a sufficient amount of siloxane (e.g. PDMS) material that provides
the desired repellency properties, as described herein.
[0044] In some embodiments, the silicone material is a compound,
oligomer or polymer having a polysiloxane backbone and more
typically a polydimethylsiloxane backbone. The polysiloxane
backbone may further comprise pendent groups, such as hydrocarbon
(e.g. preferably alkyl) groups. Such pendent groups contain more
than one carbon atoms. The silicone material typically does not
comprise vinyl groups or other polymerizable groups that would
result in the silicone material forming a crosslinked network.
[0045] In some embodiments, the siloxane (e.g. PDMS) material (e.g.
oligomer or polymer) comprises at least 50, 55, 60, 65, 70, 75, 80,
85, 90 or 95 wt.-% polydimethylsiloxane backbone. The siloxane
(e.g. PDMS) material may further comprise pendent longer chain
hydrocarbon (e.g. preferably alkyl) groups in an amount of at least
5, 10, 15, 20, 25, 30, or 35 wt.-% of the siloxane (e.g. PDMS)
material.
[0046] The siloxane (e.g. PDMS) oligomer may have a molecular
weight (Mn) of at least 1500 or 2000 g/mole as measured by GPC. The
siloxane oligomer typically has a molecular weight (Mn) no greater
than 10,000, 9000, 8000, or 7000 g/mole. The siloxane (e.g. PDMS)
polymer typically has a molecular weight (Mn) greater than 10,000;
15,000; or 20,000 g/mole. In some embodiments, the molecular weight
of the siloxane polymer is no greater than 100,000; 75,000; or
50,000 g/mole.
[0047] In some embodiments, the siloxane (e.g. PDMS) material
comprises pendent longer chain hydrocarbon (e.g. preferably alkyl)
groups wherein the longer chain hydrocarbon (e.g. preferably alkyl)
groups average at least 8, 10, 12, 14, 16, 18, or 20 carbon atoms.
In some embodiments, the siloxane (e.g. PDMS) material comprises
pendent longer chain hydrocarbon (e.g. preferably alkyl) groups
wherein the longer chain hydrocarbon (e.g. preferably alkyl) groups
average greater than 20 carbons atoms such as at least 25, 30, 35,
or 40. The pendent longer chain hydrocarbon (e.g. preferably alkyl)
groups typically average no greater than 75, 70, 65, 60, or 50
carbon atoms.
[0048] In some embodiments, the siloxane (e.g. PDMS) material may
be characterized as an alkyl dimethicone. The alkyl dimethicone
comprises at least one linear, branched, or cyclic alkyl group
averaging at least 8, 10, or 12 carbon atoms such as lauryl
dimethicone, depicted as follows:
##STR00001##
[0049] In some embodiments, the alkyl dimethicone comprises at
least one linear, branched, or cyclic alkyl group averaging at
least 14, 16, or 18 carbon atoms such as cetyl dimethicone and
stearyl dimethicone.
[0050] These materials are characterized by having a (e.g. linear)
polysiloxane backbone having terminal alkyl (C1-C4, typically
methyl) silane groups and a pendent (e.g. linear) alkyl group.
[0051] Preferred alkyl dimethicones typically have the
structure:
##STR00002##
wherein the sum of (a+b+c) is between about 100 and 1000, for
example between about 200 and 500 or between about 300 and 400; the
ratio of a to the sum of (b+c) is about 99.9:0.1 to 80:20, or about
99:1 to 85:15, or about 99:1 to 90:10, or about 99:1 to 92:8, or
about 98:2 to 93:7 or about or about 98:2 to 94:6; R.sup.1 is a
linear, branched, or cyclic alkyl group having between 20 and 50
carbon atoms, for example about 22 to 46 carbon atoms, or about 24
to 40 carbon atoms; R.sup.2 is a linear, branched, or cyclic alkyl
or alkaryl group having between 2 and 16 carbons, for example about
4 to 16, or about 5 to 12, or about 6, to 10, or about 8 carbon
atoms; and the structure is a random, block, or blocky structure.
In some embodiments, the ratio of a to (b+c) in conjunction with
the number of carbons in the R.sup.1 and R.sup.2 groups result in
an alkyl dimethicones having greater than about 50 wt. % dimethyl
siloxane (a) units, or in embodiments greater than about 60 wt. %
dimethyl siloxane units. In some embodiments, c is 0. In some
embodiments, the sum of (a+b+c) is about 300 to 400 and the ratio
of "a" to the sum of (b+c) is about 98:2 to 94:6. In some
embodiments, the alkyl dimethicone is a blend of two or more
species thereof, wherein the species differ in terms of the sum of
(a+b+c), the ratio of "a" to the sum of (b+c), the value of c, or
in two or more such parameters. In some embodiments, the alkyl
dimethicone is a random structure. In some embodiments, R.sup.1 is
a linear alkyl group. In some embodiments, R.sup.2 is a linear
alkyl group.
[0052] The alkyl dimethicone materials of the Formula I above are
characterized by having a (e.g. linear) polysiloxane backbone
having terminal alkyl (C1-C4, typically methyl) silane groups and a
plurality of pendent (e.g. linear) alkyl groups.
[0053] Methods of synthesizing alkyl dimethicones are known in the
art. See for example U.S. Pat. No. 9,187,678; incorporated
(entirely) herein by reference.
[0054] While the structures of alkyl dimethicones are generally
preferably linear structures, it will be understood by those of
skill that such structures as synthesized or purchased can include
an (e.g. small) amount of branching. Such branching, using
terminology understood by those of skill, is referred to as "T" and
"Q" functionality. In any of the embodiments herein, a
substantially linear alkyl dimethicone structure can contain an
amount of T branching, Q branching, or both.
[0055] In some embodiments, the siloxane (e.g. alkyl dimethicone)
material has a melting temperature (e.g. peak endotherm as measured
by DSC) of at least 140.degree. F. (60.degree. C.) or 150.degree.
F. (65.6.degree. C.) ranging up to 170.degree. F. (76.7.degree.
C.), 175.degree. F. (79.4.degree. C.), or 180.degree. F.
(82.2.degree. C.).
[0056] In some embodiments, the siloxane (e.g. PDMS) material may
be characterized as a high molecular weight or ultra high molecular
weight (UHMW) polydimethylsiloxane (e.g. melt additive) material.
In some embodiments, the siloxane (e.g. PDMS) material has a
viscosity of at least 10,000 centistokes; 25,000 centistokes; or
50,000 centistokes ranging up to 100,000 centistokes. In other
embodiments, the siloxane (e.g. PDMS) material has a viscosity at
25.degree. C. greater than 100,000 centistokes. The viscosity may
be at least 250,000 mPa centistokes; 500,000 mPa centistokes;
1,000,000 mPa centistokes; or 5,000,000 centistokes; and typically
less than 10,000,000 centistokes mPa. In yet other embodiments, the
siloxane (e.g. PDMS) material may be characterized as an ultra high
molecular weight (UHMW) siloxane (e.g. PDMS) material having a
viscosity greater than 10 million centistokes ranging up to 50
million centistokes.
[0057] The high and ultra high molecular weight siloxane (e.g.
PDMS) material typically comprises little or no material having a
viscosity less than 10,000 centistokes, or less than 5,000
centistokes, or less than 2500 centistokes, or less than 1000
centistokes. The ultra high molecular weight (UHMW) siloxane (e.g.
PDMS) material typically comprises little or no material having a
viscosity within the 10,000 centistokes to 100,000 centistokes.
Further, the ultra high molecular weight (UHMW) siloxane (e.g.
PDMS) material typically comprises little or no material having a
viscosity within the 100,000 centistokes to 1,000,000 mPa
centistokes. When the siloxane material comprises little or no
siloxane (e.g. PDMS) material of certain viscosities, the amount is
less than 5, 4, 3, 2, 1, 0.5 or 0.1 wt.-% based on the total weight
of the siloxane (e.g. PDMS) material. Unless specified otherwise,
the viscosity values described herein refer to those measured at a
temperature of 25.degree. C. and a shear rate of 1 sec.sup.-1.
[0058] Siloxane material melt additives often comprise a
polydimethylsiloxane backbone. Some of the methyl groups can be
substituted with functional groups to adjust the compatibility and
mobility within the thermally processible polymer.
Addition-reaction silicone elastomers, such as poly-vinyl siloxane
(i.e. vinyl polysiloxane) are a viscous liquid that cure (i.e.
chemically crosslink vinyl or other reactive groups) into a
rubber-like solid, taking the shape or profile of the surface it is
in contact with while curing. Such materials may be characterized
as thermosets. Unlike addition-reaction silicone elastomers, in
some embodiments the siloxane (e.g. PDMS) material melt additives
are not chemically crosslinked and generally do not contain
appreciable amounts of ethylenically unsaturated groups, such as
vinyl groups or other reactive groups. In other embodiments, some
of the PDMS may comprise dimethylvinyl terminal groups. Further,
some of the PDMS may be hydroxyl terminated. The concentration of
such ethylenically unsaturated groups (e.g. vinyl) or other
reactive groups is typically sufficiently low such that the
siloxane material is a thermoplastic material and/or suitable for
thermally processing after chemical crosslinking of such
groups.
[0059] In some embodiments, the siloxane (e.g. PDMS) material melt
additives are commercially available preblended with a thermally
processible polymer as a "masterbatch". For example, ultra high
molecular weight (UHMW) polydimethylsiloxane, having a siloxane
content of 50% is available predispered in low density polyethylene
(LDPE), melt flow index 8, from Dow Corning.TM. under the trade
designation "MB50-002 Masterbatch". In some embodiments the LDPE
may also contain silica (e.g. talc). Although the masterbatch is a
solid material typically in the form of pellets or a powder,
according to literature the siloxane (e.g. PDMS) material contained
therein flows like a molten polymer, yet can have a higher
molecular weight than silicone oils typically utilized as
lubricants of a lubricant impregnated surface.
[0060] The component (e.g. liner) of the spray application system
is preferably prepared in a manner such that the siloxane (e.g.
PDMS) material melt additive sufficiently separates from the
thermally processible polymer it is admixed with and migrates to
the surface of the component. When the separation or migration of
siloxane (e.g. PDMS) material melt additive is insufficient, a
liquid (e.g. paint) repellent surface, as described herein, is not
obtained. An insufficient concentration of siloxane (e.g. PDMS)
material melt additive can also result in not obtaining a liquid
(e.g. paint) repellent surface. In some embodiments, the component
or liquid (e.g. paint) repellent surface may be subjected to a heat
treatment to facilitate the separation of the siloxane (e.g. PDMS)
material melt additive from the bulk of the thermally processible
polymer. Such heat treatment may occur for example, when a liner is
thermoformed from a sheet prepared by extrusion, the liner may have
better liquid (e.g. paint) repellency than the sheet from which it
was prepared.
[0061] In some embodiments, the siloxane material may be
characterized as a siloxane copolymer or silicone-containing
copolymer. The above described alkyl dimethicone is one class of
siloxane copolymer. However, other classes of siloxane copolymers
are also suitable.
[0062] Siloxane copolymers are generally prepared using methods
such as living anionic polymerization, ring-opening polymerization
(ROP), atom transfer radical polymerization (ATRP), and step-growth
polymerization. Siloxane copolymers may be characterized for
example as grafted, segmented, or block copolymers. The block
copolymers, can have various structures, most commonly a diblock or
triblock structure.
[0063] Although the most common siloxane polymer backbone is
polydimethylsiloxane (PDMS), the backbone of the siloxane polymer
may include other substituents or polymerized units derived from
other monomers, especially non-reactive polymerized units such a
methyl phenyl siloxane, diphenyl siloxane, or
3,3,3-trifluoropropylmethyl siloxane, and combinations thereof.
[0064] The polydiorganosiloxane ("polysiloxane") backbone comprises
repeating unit of the formula:
##STR00003##
wherein each R is independently a C.sub.1-13 monovalent organic
group. For example, R can be a C.sub.1-C.sub.13 alkyl,
C.sub.1-C.sub.13 alkoxy, C.sub.2-C.sub.13 alkenyl group,
C.sub.2-C.sub.13 alkenyloxy, C.sub.3-C.sub.6 cycloalkyl,
C.sub.3-C.sub.6 cycloalkoxy, C.sub.6-C.sub.14 aryl,
C.sub.6-C.sub.10 aryloxy, C.sub.7-C.sub.13 arylalkyl,
C.sub.7-C.sub.13 aralkoxy, C.sub.7-C.sub.13 alkylaryl, or
C.sub.7-C.sub.13 alkylaryloxy. In an embodiment, where a
transparent polysiloxane-polycarbonate is desired, R is preferably
unsubstituted by halogen. Combinations of the foregoing R groups
can be used in the same copolymer.
[0065] The value of E in the above formula can vary. Generally, E
has an average value of at least 2, 5, or 10 and in some
embodiments at least 15, 20, 25, 30, 35, or 40. In typical
embodiments E has an average value up to 1,000. In some
embodiments, E is no greater than 900, 800, 700, 600 500, 400, 300,
200, or 100. In some embodiments, E is no greater than 90, 80, 70,
or 60.
[0066] In some embodiments, the siloxane copolymer comprises 50,
55, 60, 65, 70, 75, 80, 85, 90 or 95 wt.-% of polyorganosiloxane
(e.g. PDMS) material, such as in the case of the previously
described alkyl dimethicone. In other embodiments, the siloxane
copolymer comprises less than 50 wt.-% polyorganosiloxane (e.g.
PDMS) material. In some embodiments, the siloxane copolymer
comprises at least 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5 or 5 wt.-% of
polyorganosiloxane (e.g. PDMS) material. In other embodiments, the
siloxane copolymer comprises at least 10, 15, 20, 25, or 30 wt.-%
of polyorganosiloxane (e.g. PDMS) material.
[0067] Although in the case of the alkyl dimethicone copolymer
depicted above, the alkyl group is bonded directly to a silicone
atom of a siloxane backbone, when the siloxane copolymer is
prepared from other synthetic routes the silicone copolymer may
further comprise other groups within the copolymer. In such
embodiments, the silicone copolymer may be characterized as a
silicone urea copolymer, silicone-urethane copolymer,
silicone-ester copolymer, silicone amide copolymer, silicone imide
copolymer, etc.
[0068] The comonomer of the siloxane copolymer can be selected
based on the composition of the component of the spray application
system and/or based on the intended method of making the component
or repellent surface thereof.
[0069] For example when the component of the spray application
system is a thermally processible material such as a polyolefin
(e.g., LDPE) and the repellent surface is prepared by use of a
siloxane material melt additive, the siloxane copolymer melt
additive may be an alkyl dimethicone copolymer or a copolymer of
polyolefin and polyorganosiloxane (e.g. PDMS). Other siloxane
copolymers that include polyolefin are various block copolymers
such as described in U.S. Pat. Nos. 5,618,903; 5,641,835 and
5,728,469; incorporated herein by reference. As yet another
example, when the component of the spray application system
comprises polycarbonate, the siloxane copolymer melt additive may
be a polycarbonate siloxane copolymer.
[0070] Depending on the selection of the comonomer, the siloxane
(e.g. copolymer) material may have a higher melting point or higher
softening point than the alkyl dimethicone copolymer depicted
above. For example, in some embodiments, the Vicat Softening
Temperature (ASTM D 1525, Rate A/50) of the (e.g. polycarbonate)
siloxane copolymer is at least 150.degree. F. (65.6.degree. C.),
200.degree. F. (93.3.degree. C.) or 250.degree. F. (121.1.degree.
C.) ranging up to 275.degree. F. (135.degree. C.) or 300.degree. F.
(148.9.degree. C.). Highly crosslinked (e.g. thermoset) siloxane
materials generally do have a softening temperature in the ranges
just described.
[0071] In one embodiment, the polycarbonate siloxane copolymer
comprises structural units of the formula:
##STR00004##
where x and y are integers representing the number of repeating
units; and x is at least one.
[0072] Such structural units may be characterized as the A block of
a block copolymer.
[0073] The polycarbonate siloxane copolymer further comprises
polycarbonate structural units. In typical embodiments, the
polycarbonate structural unit has the formula:
##STR00005##
Such structural units may be characterized as the B block of a
block copolymer. Other aromatic polycarbonate structural units are
depicted as follows:
##STR00006##
[0074] In one embodiment, the siloxane copolymer comprises
structural units of the formula:
##STR00007##
wherein x, y, and z of the polycarbonate siloxane copolymer or
structural units thereof are integers representing the number of
repeating units of the Formulas. The integer x is at least 1 and
typically falls within the same range as E, as previously
described. The integer y is at least one and typically less than 15
or 10. In some embodiments, z ranges from 50 to 400.
[0075] According to US2013/0186799, incorporated herein by
reference, Formula V provides the molecular structure of the
polycarbonate (PC) siloxane resin LEXAN.TM. EXL 1414T resin.
[0076] Since the LEXAN.TM. copolymers are (e.g. transparent)
thermally processible thermoplastic resins, such copolymers can be
used to make liquid repellent components (e.g. liquid reservoir,
liner, lid) of the spray application system utilizing various
thermal processing techniques such as injection molding and
thermoforming.
[0077] In some embodiments, at least the repellent surface layer is
prepared from a (e.g. transparent) siloxane copolymer having a melt
flow rate of at least 2.5, 5 or 10 g/10 minutes at 300.degree.
C./1.2 kgf (ASTM D1238) and typically no greater than 30, 25 or 20
g/10 minutes. Mixtures of polycarbonate siloxane copolymers of
different flow properties can be used to achieve the overall
desired flow property. Highly crosslinked (e.g. thermoset) siloxane
materials generally do have melt flow indexes in the ranges just
described.
[0078] The tensile strength of the siloxane copolymer is typically
at least 40, 45, 50, 55, or 60 MPa. Further, the siloxane copolymer
can have a low elongation at break of less than 10% or 5%. In some
embodiments, the siloxane copolymer has a tensile modulus of at
least 1000, 1500, or 2000 MPa ranging up to 2500 MPa. The tensile
and elongation properties can be measured according to ASTM D-638
(e.g. at a rate of 50 mm/min).
[0079] PDMS generally has a melting point of about -40.degree. C.
and a glass transition temperature (Tg) of about -125.degree. C.
Siloxane copolymers can have melting point and glass transition
temperatures greater than 0.degree. C. or greater than 25.degree.
C. In some embodiments, the siloxane copolymer has a melt
temperature of at least 100.degree. C., 150.degree. C., 200.degree.
C., 250.degree. C., or 300.degree. C. and typically no greater than
350.degree. C. or 400.degree. C. In some embodiments, the siloxane
copolymer has a Tg of at least 50.degree. C., 75.degree. C.,
100.degree. C., 125.degree. C., or 150.degree. C. and typically no
greater than 175.degree. C. or 200.degree. C. Unless specified
otherwise, thermal properties can be determined by Differential
Scanning calorimetry (DSC).
[0080] In some embodiments, the repellent surface can be prepared
by providing a repellent surface layer on a spray application
system component (e.g. liquid reservoir, liner, lid) formed by
application of an organic solvent-coating composition comprising
siloxane material such as a polycarbonate-siloxane copolymer to a
spray application system component.
[0081] Various organic polymeric binders can be utilized. Although
fluorinated organic polymeric binders can also be utilized,
fluorinated organic polymeric binders are typically considerably
more expensive than non-fluorinated binders. Further,
non-fluorinated organic polymeric binders can exhibit better
adhesion to polymeric components (e.g. reservoir, liner, or lid) of
the spray application system.
[0082] Suitable non-fluorinated binders include for example
polystyrene, atactic and syndiotactic polystyrene, acrylic (i.e.
poly(meth)acrylate), polyester, polyurethane (including polyester
type thermoplastic polyurethanes "TPU"), polyolefin (e.g.
polyethylene), and polyvinyl chloride. Many of the polymeric
materials that the component (e.g. reservoir, liner, or lid) of the
spray application system can be thermally processed from, as will
subsequently be described, can be used as the non-fluorinated
organic polymeric binder of an (e.g. organic solvent) coating
composition. However, in typical embodiments, the non-fluorinated
organic polymeric binder is a different material than the polymeric
material of the component. In some embodiments, the organic
polymeric binder typically has a receding contact angle with water
of less than 90, 80, or 70 degrees. Thus, the binder is typically
not a siloxane (e.g. PDMS) material.
[0083] In some embodiments, the (e.g. non-fluorinated) organic
polymeric binder is a film-grade resin, having a relatively high
molecular weight. Film-grade resins can be more durable and less
soluble in an organic solvent that may be present in the liquid
(e.g. paint) being repelled. In other embodiments, the (e.g.
non-fluorinated) organic polymeric binder can be a lower molecular
weight film-forming resin. Film-forming resins can be more
compliant and less likely to affect the collapsibility of a liquid
(e.g. paint) reservoir or liner. Viscosity and melt flow index are
indicative of the molecular weight. Mixtures of (e.g.
non-fluorinated) organic polymeric binder can also be used.
[0084] In some embodiments, the film-grade (e.g. non-fluorinated)
organic polymeric binder typically has a melt flow index of at
least 1, 1.5, 2, 2.5, 3, 4, or 5 g/10 min at 200.degree. C./5 kg
ranging up to 20, 25, or 30 g/10 min at 200.degree. C./5 kg. The
melt flow index can be determined according to ASTM D-1238. The
tensile strength of the (e.g. non-fluorinated) organic polymeric
binder is typically at least 40, 45, 50, 55, or 60 MPa. Further,
the (e.g. non-fluorinated) organic polymeric binder can have a low
elongation at break of less than 10% or 5%. The tensile and
elongation properties can be measured according to ASTM D-638. Such
film-grade (e.g. non-fluorinated) organic polymeric binders just
described can also be suitable for use as a thermally processible
polymer of the spray application system component (e.g. reservoir,
liner, lid).
[0085] In other embodiments, the (e.g. non-fluorinated) organic
polymeric binders have a lower molecular weight and lower tensile
strength than film-grade polymers. In one embodiment, the melt
viscosity of the (e.g. non-fluorinated) organic polymeric binders
(as measured by ASTM D-1084-88) at 400.degree. F. (204.degree. C.)
ranges from about 50,000 to 100,000 cps. In another embodiment, the
molecular weight (Mw) of the (e.g. non-fluorinated) organic
polymeric binder is typically at least about 1000, 2000, 3000,
4000, or 5000 g/mole ranging up to 10,000; 25,000; 50,000; 75,000;
100,000; 200,000; 300,000; 400,000, or 500,000 g/mole. In some
embodiments, the (e.g. non-fluorinated) organic polymeric binder
has a tensile strength of at least 5, 10, or 15 MPa ranging up to
25, 30 or 35 MPa. In other embodiments, the (e.g. non-fluorinated)
organic polymeric binder has a tensile strength of at least 40, 45,
or 50 MPa ranging up to 75 or 100 MPa. In some embodiments, the
(e.g. non-fluorinated) organic polymeric binder has an elongation
at break ranging up to 25, 50, 100, 200, 300, 400, 500, 600, 700,
800, 900 or 1000% or higher. In some embodiments, the (e.g.
non-fluorinated) organic polymeric binder has a Shore A hardness of
at least 50, 60, 70, or 80 ranging up to 100.
[0086] In some embodiments, the (e.g. non-fluorinated) organic
polymeric binder is selected such that it is (e.g. mechanically)
compliant at the use temperature of the coated substrate or
article.
[0087] In this embodiment, the (e.g. non-fluorinated) organic
polymeric binder has a glass transition temperature (Tg) as can be
measured by DSC of less than 0.degree. C. or 32.degree. F. In some
embodiments, the (e.g. non-fluorinated) organic polymeric binder
has a glass transition temperature (Tg) of less than 20.degree. F.,
10.degree. F., 0.degree. F., -10.degree. F., -20.degree. F.,
-30.degree. F., -40.degree. F., -50.degree. F., -60.degree. F.,
-70.degree. F., or -80.degree. F. In some embodiments, the (e.g.
non-fluorinated) organic polymeric binder has a Tg of at least
-130.degree. C. The selection of (e.g. non-fluorinated) organic
polymeric binder can contribute to the durability of the repellent
surface.
[0088] In typical embodiments, the non-fluorinated organic
polymeric binder typically does not form a chemical (e.g. covalent)
bond with the siloxane (e.g. PDMS) material as this may hinder the
migration of the siloxane (e.g. PDMS) material to the outermost
surface layer.
[0089] In some embodiments, the (e.g. non-fluorinated) organic
polymeric binder is not curable, such as in the case of alkyd
resins. An alkyd resin is a polyester modified by the addition of
fatty acids and other components. They are derived from polyols and
a dicarboxylic acid or carboxylic acid anhydride. Alkyds are the
most common resin or "binder" of most commercial "oil-based" paints
and coatings.
[0090] In some embodiments, the selection of the non-fluorinated
polymeric binder can affect the concentration of siloxane (e.g.
PDMS) material that provides the desired liquid (e.g. paint)
repellency properties.
[0091] The siloxane (e.g. PDMS) polymers or compositions comprising
a siloxane (e.g. PDMS) material and a non-fluorinated organic
polymeric binder can be dissolved, suspended, or dispersed in a
variety of organic solvents to form coating compositions suitable
for use in coating the compositions onto a substrate or component
of a spray application system. The organic coating compositions
typically contain at least about 85%, 86%, 87%, 88%, 89%, 90%, 91%,
92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% organic solvent or greater,
based on the weight of the coating composition. The coating
compositions typically contain at least about 0.01%, 0.1%, 0.5%,
1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15% or greater solids of
(e.g. non-fluorinated) organic polymeric binder and siloxane (e.g.
PDMS) material, based on the total weight of the coating
composition. However, the coating composition can be provided as a
concentrate with an even higher amount of solids, e.g. 20, 30, 40,
or 50 wt.-% solids. Suitable solvents include for example alcohols,
esters, glycol ethers, amides, ketones, hydrocarbons,
chlorohydrocarbons, hydrofluorocarbons, hydrofluoroethers,
chlorocarbons, and mixtures thereof. In some embodiments, the
coating composition is an aqueous suspension, emulsion, or solution
comprising at least 50 wt.-% or greater water and an organic
cosolvent.
[0092] In one embodiment, the coating composition may contain 5
wt.-% of low density polyethylene binder (such as the NA217000 LDPE
or Marflex 1122 LDPE described in the forthcoming examples)
dissolved is 95 wt.-% or organic solvent, such as xylene, toluene,
or dichloroethylene. The coating composition may further contain 3
wt.-% of siloxane material (such as SMA described in the
forthcoming examples). Other concentrations of binder and siloxane
material can be utilized provided the desired liquid repellency
properties are attained.
[0093] The coating compositions may contain one or more additives
provided the inclusion of such does not detract from the liquid
(e.g. paint) repellent properties.
[0094] The coating compositions can be applied to a substrate or
component by standard methods such as, for example, spraying,
padding, dipping, roll coating, brushing, or exhaustion (optionally
followed by the drying of the treated substrate to remove any
remaining water or organic solvent). The substrate can be in the
form of sheet articles that can be subsequently thermally formed
into a liquid (e.g. paint) reservoir, liner or lid. When coating
flat substrates of appropriate size, knife-coating or bar-coating
may be used to ensure uniform coatings of the substrate.
[0095] The moisture content of the organic coating composition is
preferably less than 1000, 500, 250, 100, or 50 ppm. In some
embodiments, the coating composition is applied to the substrate at
a low relative humidity, e.g. of less than 40%, 30%, or 20% at
25.degree. C.
[0096] The coating compositions can be applied at an amount
sufficient to achieve the desired repellency properties. Coatings
as thin as 250, 300, 350, 400, 450, or 500 nm ranging up to 1, 1.5,
2, 2.5, 3, 3.5, 4, 4.5 or 5 microns can provide the desired
repellency. However, thicker coatings (e.g., up to about 10, 15, 20
microns or more) can also be used. Thicker coatings can be obtained
by applying to the substrate a single thicker layer of a coating
composition that contains a relatively high concentration of
solids. Thicker coatings can also be obtained by applying
successive layers to the substrate.
[0097] In another embodiment, the siloxane (e.g. PDMS) material can
be combined with a thermally processible (e.g. thermoplastic)
polymer and then melt processed into a surface layer, substrate, or
component such as a liquid (e.g. paint) repellent reservoir, liner
or lid. In this embodiment, the siloxane (e.g. PDMS) material
typically migrates to the surface forming a surface layer with a
high concentration of siloxane material relative to the total
amount of siloxane material and thermally processible polymer.
[0098] In typical embodiments, the amount of siloxane (e.g. PDMS)
material (melt additive) is at least about 0.05, 0.1, 0.25, 0.5,
1.5, 2.0 or 2.5 wt.-% and in some embodiments, at least about 3.0,
3.5, 4.0, 4.5 or 5 wt.-%. The amount of siloxane material is
typically no greater than 25, 20, 15, or 10 wt.-% of the sum of the
siloxane (e.g. PDMS) material (melt additive) and thermally
processible polymer.
[0099] To form a polymer blend by melt processing, the siloxane
material can be, for example, mixed with pelletized, granular,
powdered or other forms of the thermally processible polymer and
then melt processed by known methods such as, for example, molding
or melt extrusion. The siloxane (e.g. PDMS) material can be mixed
directly with the thermally processible polymer or it can be mixed
with the (thermally processible) polymer in the form of a "master
batch" (concentrate) of the siloxane (e.g. PDMS) material in the
(same or similar) polymer as the thermally processible polymer. If
desired, an organic solution of the siloxane (e.g. PDMS) material
can be mixed with powdered or pelletized polymer, followed by
drying (to remove solvent) and then melt processing. Alternatively,
the siloxane (e.g. PDMS) composition can be added to the polymer
melt to form a mixture or injected into a molten polymer stream to
form a blend immediately prior to extrusion or molding into
articles.
[0100] In some embodiments, the melt processible (e.g.
thermoplastic) polymer is a polyolefin, polyester, polyamide,
polyurethane, polycarbonate, polystyrene, poly(alkyl acrylate), or
polyacrylate. The thermoplastic polymer preferably is a polyolefin,
mixture or blend of one or more polyolefins, a polyolefin
copolymer, mixture of polyolefin copolymers, or a mixture of at
least one polyolefin and at least one polyolefin copolymer.
[0101] The thermoplastic polymer is more preferably a polyolefin
polymer or copolymer wherein the polymer unit or copolymer unit is
ethylene, propylene, butylene, hexene or mixtures thereof. Thus the
polyolefin is preferably polypropylene, polyethylene, polybutylene,
polyhexylene or a blend or copolymer thereof. Oher polyolefins
include poly-.alpha.-olefins, and copolymers thereof, including low
density polyethylene (LDPE), high density polyethylene (HDPE),
linear low density polyethylene (LLDPE), ultra-high density
polyethylene (UHDPE), and polyethylene-polypropylene copolymers, as
well as polyolefin copolymers having non-olefin content (that is,
content derived from monomers that are not olefins). The non-olefin
content of polyolefin polymers employed in some embodiments is not
particularly limited, but includes, for example, 1-5 wt % of
acrylic acid, or methacrylic acid functionality, including sodium,
zinc, or calcium salts of the acid functionality; 1-5 wt % of an
anhydride functionality, such as maleic anhydride, or the
corresponding ring-opened carboxylate functionality; and the like.
In some embodiments, blends of polyolefins containing
non-polyolefin content are blended at various ratios with
polyolefins in order to provide a targeted level of non-olefin
content.
[0102] In one embodiment, the thermoplastic polymer is polyethylene
having a melting point ranging from 90-140.degree. C. such as
available from Chevron Phillips under the trade designation
"MarFlex 1122 Polyethylene".
[0103] The siloxane melt additives are generally a solid at room
temperature (e.g. 25.degree. C.) and at the use temperature of the
spray application system component, which commonly ranges from
40.degree. F. to 120.degree. F. The siloxane (e.g. PDMS) material
and thermally processible polymer are selected such that the
siloxane material is typically molten at the melt processing
temperature of the mixture. In some embodiments, the siloxane
material has a melt temperature no greater than 200, 190, 180, 170,
or 160.degree. C. In other embodiments, the melt temperature may be
higher.
[0104] The melt processible polymer of the repellent surface and/or
component (e.g. reservoir, liner, lid) may further contain
non-siloxane slip agents, anti-blocks (e.g. silica, talc)
antioxidants, tints, antistatic agents, light stabilizers,
clarifiers, nucleating agents, and other additives known in the
art. Clarifiers typically increase the clarity by reducing the size
of the spherulites. Smaller spherulites allow more light through
the polymer, which decreases the haze of the part. Unlike
nucleating agents, clarifiers are transparent, which also helps to
decrease haze values.
[0105] Extrusion can be used to form polymeric films. In film
applications, a film forming polymer is simultaneously melted and
mixed as it is conveyed through the extruder by a rotating screw or
screws and then is forced out through a slot or flat die, for
example, where the film is quenched by a variety of techniques
known to those skilled in the art. The films optionally are
oriented (after being cast) prior to quenching by drawing or
stretching the film at elevated temperatures in the machine and/or
transverse directions simultaneously or sequentially.
[0106] Molded articles are produced by pressing or by injecting
molten polymer from a melt extruder as described above into a mold
where the polymer solidifies. Typical melt forming techniques
include injection molding, blow molding, compression molding and
extrusion, and are well known to those skilled in the art. The
molded article is then ejected from the mold and optionally
heat-treated to effect migration of the polymer additives to the
surface of the article.
[0107] In some embodiments, a molded component with a
liquid-repellent surface may be made using molding processes (e.g.
co-injection molding or bi-injection molding) in which two
different resins are injected into a mold through the same gate or
different gates to form an integral liquid-repellent skin layer
over a core layer in a single molding process. For example, the
first of the two resins could be a polyolefin, and the second of
the two resins could be a polyolefin to which a neat melt additive
or melt additive masterbatch has been added.
[0108] After melt processing, an annealing step can be carried out
to enhance the development of repellent characteristics. The
annealing step typically is conducted below or above the melt
temperature of the polymer for a sufficient period of time. The
annealing step can be optional.
[0109] The repellent surface layer described herein can be provided
on a wide variety of organic or inorganic components.
[0110] In some embodiments, different components are coated with
different solid materials. In other embodiments, the surface of one
portion of a component can comprise one type of a solid liquid
(e.g. paint) repellent material and another surface portion can
comprise a different type of solid material. Likewise, the surface
of one portion of a component can comprise one type of a solid
liquid (e.g. paint) repellent material and another surface portion
can comprise a different liquid (e.g. paint) repellent
material.
[0111] In typical embodiments, the entire surface of the component
(e.g. reservoir, liner or lid) of the spray application system that
normally comes in contact with a liquid (e.g. paint) comprises a
liquid (e.g. paint) repellent surface as described herein. In other
embodiments, only a portion of the surface of the component (e.g.
reservoir, liner or lid) of the spray application system that
normally comes in contact with a liquid (e.g. paint) comprises a
liquid (e.g. paint) repellent surface as described herein. This
latter embodiment is still beneficial relative to components
lacking a liquid (e.g. paint) repellent surface.
[0112] Suitable polymeric materials for components include, but are
not limited to, polyesters (e.g., polyethylene terephthalate or
polybutylene terephthalate), polycarbonates, acrylonitrile
butadiene styrene (ABS) copolymers, poly(meth)acrylates (e.g.,
polymethylmethacrylate, or copolymers of various (meth)acrylates),
polystyrenes, polysulfones, polyether sulfones, epoxy polymers
(e.g., homopolymers or epoxy addition polymers with polydiamines or
polydithiols), polyolefins (e.g., polyethylene and copolymers
thereof or polypropylene and copolymers thereof), polyvinyl
chlorides, polyurethanes, fluorinated polymers, cellulosic
materials, derivatives thereof, and the like.
[0113] In some embodiments, where increased transmissivity is
desired, the polymeric component can be transparent. The term
"transparent" means transmitting at least 85 percent, at least 90
percent, or at least 95 percent of incident light in the visible
spectrum (wavelengths in the range of 400 to 700 nanometers).
Transparent components may be colored or colorless.
[0114] Suitable inorganic substrates include metals and siliceous
materials such as glass. Suitable metals include, for example, pure
metals, metal alloys, metal oxides, and other metal compounds.
Examples of metals include, but are not limited to, chromium, iron,
aluminum, silver, gold, copper, nickel, zinc, cobalt, tin, steel
(e.g., stainless steel or carbon steel), brass, oxides thereof,
alloys thereof, and mixtures thereof.
[0115] The siloxane materials described herein can render the
coated surface hydrophobic. The terms "hydrophobic" and
"hydrophobicity" refer to a surface on which drops of water or
aqueous liquid exhibit an advancing and/or receding water contact
angle of at least 50 degrees, at least 60 degrees, at least 70
degrees, at least 80 degrees, at least 90 degrees, at least 95
degrees, or at least 100 degrees.
[0116] In some embodiments, the advancing and/or receding contact
angle of the repellent surface of the substrate or component with
water may increase, relative to the substrate or component lacking
a liquid (e.g. paint) repellent surface, by at least 10, 15, 20,
25, 30, 35, 40 degrees. In some embodiments, the receding contact
angle with water may increase by at least 45, 50, 55, 60, or 65
degrees.
[0117] In some embodiments, the (e.g. siloxane) materials described
herein, provide a surface that exhibits an advancing and/or
receding contact angle with water of at least 105, 110, or 115
degrees. The advancing and/or receding contact angle with water is
typically no greater than 135, 134, 133, 132, 131, or 130 degrees
and in some embodiments, no greater than 129, 128, 127, 126, 125,
124, 123, 122, 121, or 120 degrees. The difference between the
advancing and/or receding contact angles (contact angle hysteresis
("CAH")) with water of the liquid repellent surface layer can be at
least 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50 degrees. Favorably
the difference between the advancing and receding contact angle
with water of the surface treated hydrophobic lubricant impregnated
porous surface, as well as the other (e.g. solid) materials
described herein is no greater than 15, 14, 13, 12, 11, 10, 9, 8,
7, 6, 5, 4, 3, 2, or 1 degree. As the difference between the
advancing and/or receding contact angle with water increases, the
tilt angle needed to slide or roll off a (e.g. water or paint)
droplet from a planar surface increases. One of ordinary skill
appreciates that deionized water is utilized when determining
contact angles with water.
[0118] The contact angle of the liquid (e.g. paint) repellent
surface of the substrate or component can also be evaluated with
other liquids instead of water. For example, since paints, such as
water-based automobile paints, often comprise 2-n-butoxyethanol,
the contact angle of the liquid (e.g. paint) repellent surface with
a solution of 10% by weight 2-n-butoxyethanol and 90% by weight
deionized water can also be of importance. In some embodiments, the
advancing contact angle with such 2-n-butoxyethanol solution is at
least 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59,
60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70 degrees and in some
embodiments at least 75 or 80 degrees. In some embodiments, the
receding contact angle with such 2-n-butoxyethanol solution is at
least 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49,
50, 55, 60, 65, or 70 degrees. In some embodiments, the advancing
and/or receding contact angle of the liquid (e.g. paint) repellent
surface of the substrate or component with a solution of 10% by
weight 2-n-butoxyethanol and 90% by weight deionized water is no
greater than 100, 95, 90, 85, 80, or 75 degrees.
[0119] In another embodiment, the contact angle of the liquid (e.g.
paint) repellent surface of the substrate or component with
hexadecane is at least 45, 46, 47, 48, 49, 50, 55, 60, 65, 70, or
75 degrees. The advancing contact angle with hexadecane is
typically at least 45, 50, 55, 60, 65, 70, 75, 80, or 84 degrees.
In typical embodiments, the receding or advancing contact angle
with hexadecane is no greater than 85 or 80 degrees.
[0120] The (e.g. siloxane) materials described herein can be used
to impart or enhance (e.g. aqueous) liquid repellency of a variety
of substrates.
[0121] The term "aqueous" means a liquid medium that contains at
least 50, 55, 60, 65, or 70 wt-% of water. The liquid medium may
contain a higher amount of water such as at least 75, 80, 85, 90,
95, 96, 97, 98, 99, or 100 wt.-% water. The liquid medium may
comprise a mixture of water and one or more water-soluble organic
cosolvent(s), in amounts such that the aqueous liquid medium forms
a single phase. Examples of water-soluble organic cosolvents
include for example methanol, ethanol, isopropanol,
2-methoxyethanol, (2-methoxymethylethoxy)propanol,
3-methoxypropanol, 1-methoxy-2-propanol, 2-butoxyethanol, ethylene
glycol, ethylene glycol mono-2-ethylhexylether, tetrahydrofuran,
2,2,4-trimethyl-1,3-pentanediol monoisobutyrate, tetraethylene
glycol di(2-ethylhexoate), 2-ethylhexylbenzoate, and ketone or
ester solvents. The amount of organic cosolvent does not exceed 50
wt-% of the total liquids of the coating composition. In some
embodiments, the amount of organic cosolvent does not exceed 45,
40, 35, 30, 25, 20, 15, 10 or 5 wt.-% organic cosolvent. Thus, the
term aqueous includes (e.g. distilled) water as well as water-based
solutions and dispersions such as paint.
[0122] In some embodiments, the aqueous (e.g. paint) "ready to
spray" dispersions, e.g. paint, described herein may comprise at
least 5, 10, or 15 wt.-% solids with the remainder being aqueous
liquid medium. In some embodiments, the aqueous (e.g. paint) "ready
to spray" dispersions, e.g. paint, described herein may comprise at
least 20, 25, 30, or 35 wt.-% solids with the remainder being
aqueous liquid medium. Further, in some embodiments, the aqueous
(e.g. paint) dispersions may be a concentrate comprising at least
40, 45, 50, 55, 60, 65, 70, 75, 80, or 85 wt.-% solids with the
remainder being aqueous liquid medium. Such concentrates are
generally diluted to prepare an aqueous (e.g. paint) "ready to
spray" dispersion.
[0123] In some embodiments, the (e.g. solid) materials described
herein can impart a degree of aqueous liquid repellency such that
no greater than 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, or 1% of the
repellent surface area comprises an aqueous test liquid, such as
paint, after use of the spray application system or after holding
the repellent surface vertically for a specified duration of time
(e.g. 30 seconds-5 minutes or 30 minutes) and visually determining
(in the absence of a microscope) the amount of aqueous liquid (e.g.
paint). In some embodiments, polypropylene glycol (400 Mw),
butoxyethanol, or a 50 wt. % aqueous solution of butoxyethanol can
be used as a test liquid.
[0124] In some embodiments, the porous layer impregnated lubricant,
as well as the other (e.g. solid) materials described herein can
impart a degree of liquid repellency such that the mass of retained
aqueous liquid (e.g. paint) is no greater than 0.01 g/cm.sup.2,
0.005 g/cm.sup.2, 0.001 g/cm.sup.2, or 0.0005 g/cm.sup.2. In some
embodiments, polypropylene glycol (400 Mw), butoxyethanol, or a 50
wt. % aqueous solution of butoxyethanol can be used as a test
liquid.
[0125] The paint repellency can be evaluated according to any one
or combination of test methods described herein utilizing a test
paint. Various aqueous-based automotive paints were found to be
repelled by the surfaces described herein such as PPG ENVIROBASE
HIGH PERFORMANCE T409, SIKKENS AUTOWAVE, SPIES HECKER PERMAHYD
HI-TEC BASE COAT 480, and GLASURIT ADJUSTING BASE 93-E3. Unless
specified otherwise, the test paint for determining paint
repellency according to the test methods described herein was PPG
Envirobase automobile paint mixed to specification containing 90
weight % ENVIROBASE HIGH PERFORMANCE T409 DEEP BLACK and 10 weight
% ENVIROBASE HIGH PERFORMANCE T494 PAINT THINNER, available from
PPG Industries, Pittsburgh Pa. or available from 3M, St. Paul,
Minn.
[0126] The liquid (e.g. paint) repellent surface is preferably
durable such that the liquid (e.g. paint) repellency is retained
for a sufficient amount of time (e.g. the normal duration of time a
(e.g. disposable) liquid (e.g. paint) reservoir or liner is
utilized). In some embodiments, the liquid (e.g. paint) repellency
is retained after surface abrasion testing (according to the test
method described in the examples). In some embodiments, the liquid
(e.g. paint) repellency may diminish to some extent, yet remains
highly repellent after surface abrasion testing. Thus, after
surface abrasion testing the contact angles or paint repellency
meet(s) the criteria previously described.
[0127] The spray application system described herein can be
utilized to apply an aqueous liquid mixture, such as paint.
[0128] As used herein, the term "paint" refers to a composition
having an aqueous liquid medium, as previously described, and a
polymeric (e.g. latex) binder dispersed in the aqueous liquid
medium. Common polymeric binders utilized in paint include acrylic
polymers, alkyd polymers, urethane polymers, epoxy polymers, and
combinations thereof. In some embodiments, the (e.g. base coat)
paint may comprise a combination of acrylic and alkyd polymers. In
other embodiments, the (e.g. clear coat) paint may comprise
hexamethylene isocyanate oligomers and/or cyclohexyl isocyanate
oligomers at concentrations ranging from about 20 to 40 wt-% for
"ready to spray" compositions.
[0129] In the absence of opacifying pigment(s), such as titanium
dioxide, silica, carbon black, etc. or other colorant (i.e. pigment
or dye other than black or white) the paint may be characterized as
a "clear coat". Paints that further comprise opacifying pigment(s),
yet not colored pigments may be characterized as primers. Further,
paints that further comprise both opacifying pigment(s) and
colorant(s) may be characterized as base coats.
[0130] Whereas clear coats are generally free of opacifying
pigments and colorants, primers and base coats typically comprise
at least 10, 15, 20, 25 or 30 wt.-% or greater of opacifying
pigment(s) such as titanium dioxide. Base coats further comprise
colorants at various concentrations. In some embodiments, the paint
comprises 5 to 25 wt.-% of colorants.
[0131] The liquid medium may comprise relatively small
concentrations of volatile organic solvents. For example, the
volatile organic content of water-based flat architectural paint,
water-based automobile primer, and water-based clear coat is
typically no greater than 250 grams/liter and in some embodiments
no greater than 200 grams/liter, 150 grams/liter, 100 grams/liter,
or 50 grams/liter. The VOC content may be higher, ranging from at
least 275, 300, or 325 grams/liter up to 500 grams/liter,
particularly for automobile base coat. In some embodiments, the VOC
content is no greater than 450 or 425 grams/liter. Paint referred
to as no-VOC typically may contain 5 grams/liter or less of
volatile organic solvents. As used herein, VOC is any organic
compound having a boiling point less than or equal to 250.degree.
C. measured at a standard atmospheric pressure of 101.3 kPa.
[0132] As the concentration of colored pigment(s) increases, the
concentration of (e.g. volatile) organic solvents present for the
purpose of dissolving and dispersing such colored pigment(s) can
also increase. Further, (e.g. volatile) organic solvents can also
be utilized to lower the viscosity of the paint. Viscosity will
vary with the thinner level chosen. However, in some embodiments,
the viscosity of the "ready to spray" paint at 20.degree. C. ranges
from 50 to 100 cps.
[0133] The paint may comprise water-soluble organic solvents such
as alcohols (e.g. alkylene glycol alkyl ether). For example, the
paint may comprise 2-butoxyethanol (ethylene glycol monobutyl
ether), having a boiling point of 171.degree. C. (340.degree. F.);
butoxypropan-2-ol (propylene glycol n-butyl ether), having a
boiling point of 171.degree. C. (340.degree. F.);
2-(2-butoxyethoxy)ethanol (diethylene glycol monobutyl ether),
having a boiling point of 230.degree. C. (446.degree. F.); and
combinations thereof. The paint may comprise one or more of such
alcohols at a total concentration of at least 5 wt.-% ranging up to
10, 15, 20, or 25 wt.-%.
[0134] The paint may further comprise other solvents that may be
characterized as "exempt" solvents, i.e. not causing the formation
of ground level ozone (smog), according to environmental chemists.
Representative examples include acetone, ethyl acetate, tertiary
butyl acetate (TBAc), and isopropanol.
[0135] When the spray application system described herein is
utilized to apply an aqueous liquid mixture, such as paint, the
method may comprise applying more than one coat of the same or
different paint compositions. For example, in one embodiment, the
method may comprise applying one or more coats of a primer or
sealer. In another embodiment, the method may comprise applying one
or more coats of a (e.g. colored) base coat. In another embodiment,
the method may comprise applying one or more coats of a clear coat.
The method may comprise applying a combination of primer, sealer,
base coat, and/or clear coat. The method is particularly
advantageous for use with (e.g. automobile) base coats that are
substantially more expensive than primers, sealers and clear
coats.
[0136] In some embodiments, 3-4 coats may be applied (e.g. to an
automobile panel) wherein each coat, or in other words "film build
per wet coat" ranges in thickness from 0.80 to 1.0 mils. Upon
drying this can produce a dried film build ranging from about 0.10
to 0.20 mils.
[0137] In some embodiments, each coat of the method utilizes an
aqueous paint. In other embodiments, at least one coat may be an
organic solvent based paint, i.e. a paint comprising greater than
50 wt-% organic solvent that may not form a single phase with
water. Organic solvent-based paints typically do not contain any
water. For example, solvent-based clear coats may contain organic
polar and non-polar solvents such as xylene, acetone, naphtha,
alkyl benzene, toluene, heptan-2-one, and the like at a total
organic solvent concentration ranging from at least 50 wt.-%, or 60
wt.-% up to about 75 wt.-% or greater.
[0138] In one embodied method, a solvent based clear coat is
applied to a dried water based base coat.
[0139] When the paint comprises organic solvent, the
non-fluorinated polymeric binder and/or siloxane (e.g. PDMS)
material may be selected to exhibit no solubility or only trace
solubility with the organic solvent(s) of the paint, e.g., a
solubility of 0.01 grams/liter or 0.001 grams/liter or less.
[0140] Alternatively or in combination with having trace
solubility, the non-fluorinated polymeric binder and/or the
siloxane (e.g. PDMS) material may be selected such that it is
compatible with the paint and paint application methods. The
non-fluorinated polymeric binder and/or siloxane (e.g. PDMS)
material may be present in the paint at higher concentrations, i.e.
greater than 0.01 grams/liter, or greater than 0.1 grams/liter, or
greater than 0.25 grams/liter, or greater than 0.5 grams/liter; yet
still be compatible with the paint and paint application methods.
In some embodiments, non-fluorinated polymeric binder and/or
siloxane (e.g. PDMS) material may function as a paint additive and
be present in the paint at concentrations ranging from about 0.5
grams/liter to 1, 1.5, 2, 2.5, or 3 wt-% of the paint.
[0141] There are various approaches that can be taken to determine
the compatibility of the non-fluorinated polymeric binder and/or
siloxane (e.g. PDMS) material with the paint.
[0142] In one approach, when opposing major surface layers of the
dried paint comprise substantially the same concentration
(difference of less than 10, 5 or 1% relative to the major surface
having the higher concentration) of non-fluorinated polymeric
binder and/or siloxane (e.g. PDMS) material, such materials can be
characterized as chemically compatible with the paint.
[0143] In another approach, the siloxane (e.g. (PDMS) material may
be sufficiently compatible with the paint such that the presence
thereof does not affect the inter-layer adhesion of a painted
substrate. This can be evaluated according to Standard Test Method
for Measuring Adhesion by Tape Test (ASTM D3359-09). When the
cross-hatch adhesion is substantially the same relative to a
control of the same paint in the absence of the lubricant (or the
combination of lubricant and hydrophobic layer), the presence of
the lubricant (or the combination of lubricant and hydrophobic
layer) can be characterized as not affecting the inter-layer
adhesion. Typically, 90, 95, or 100% of the paint is retained after
cross-hatch adhesion testing according to ASTM D3359-09. The
non-fluorinated polymeric binder and/or siloxane (e.g. PDMS)
material may be sufficiently compatible with the paint such that
the presence thereof does not affect the inter-layer adhesion of a
painted substrate.
[0144] In yet another approach, the non-fluorinated polymeric
binder and/or siloxane (e.g. PDMS) material may be sufficiently
compatible with the paint such that the siloxane (e.g. PDMS)
material does not affect the method of applying the paint. For
example, additional coats of the same paint can be uniformly
applied at a sufficient film build as previously described. In yet
another example, additional coats of a different paint (e.g. a
clear coat applied to a dried base coat) can be uniformly applied
at a sufficient film build as previously described. Lack of
uniformity across the painted panel or substrate can typically be
visually detected by observing the occurrence of "fisheyes" or
other incompatibility-related coating defects while applying the
paint and/or by uneven gloss and/or color that can be measured
after the applied paint has dried.
[0145] The liquid repellent surface (e.g. layer) of the component
(e.g. liquid reservoir, liner, or lid) can be provided by one of
the embodied siloxane materials previously described or any
suitable combination of such siloxane materials with each other, or
any suitable combination of such siloxane material(s) with the
lubricant impregnated materials and/or fluorinated materials
described in WO2016/069674. Further, one of the components can have
a different embodied material than another component. For example,
the reservoir and/or lid may comprise Lexan.TM. 1414T; whereas the
liner comprises a thermally processible polymer and a siloxane
copolymer melt additive.
[0146] Unless specified otherwise, the following definitions are
applicable to the presently described invention.
[0147] The recitation of any numerical range by endpoints is meant
to include the endpoints of the range, all numbers within the
range, and any narrower range within the stated range.
[0148] The term "a", "an", and "the" are used interchangeably with
"at least one" to mean one or more of the elements being
described.
[0149] The term "and/or" means either or both. For example, the
expression "A and/or B" means A, B, or a combination of A and
B.
[0150] The term "alkylene" refers to a divalent group that is a
radical of an alkane and includes groups that are linear, branched,
cyclic, bicyclic, or a combination thereof. The alkylene group
typically has 1 to 30 carbon atoms. In some embodiments, the
alkylene group has 1 to 20 carbon atoms, 1 to 10 carbon atoms, 1 to
6 carbon atoms, or 1 to 4 carbon atoms.
[0151] The term "alkoxy" refers to refers to a monovalent group
having an oxy group bonded directly to an alkyl group.
[0152] The term "aryl" refers to a monovalent group that is
aromatic and carbocyclic. The aryl has at least one aromatic ring
and can have one or more additional carbocyclic rings that are
fused to the aromatic ring. Any additional rings can be
unsaturated, partially saturated, or saturated. Aryl groups often
have 6 to 20 carbon atoms, 6 to 18 carbon atoms, 6 to 16 carbon
atoms, 6 to 12 carbon atoms, or 6 to 10 carbon atoms.
[0153] The term "fluorinated" refers to a group or compound that
contains at least one fluorine atom attached to a carbon atom.
Perfluorinated groups, in which there are no carbon-hydrogen bonds,
are a subset of fluorinated groups.
[0154] Objects and advantages of this invention are further
illustrated by the following examples, but the particular materials
and amounts thereof recited in these examples, as well as other
conditions and details, should not be construed to unduly limit
this invention.
Test Methods
[0155] IR data was obtained using a Nicolet 6700 Series FT-IR
spectrometer (Thermo Scientific, Waltham, Mass.).
Method for Contact Angle Measurements
[0156] Water contact angles were measured using a Rame-Hart
goniometer (Rame-Hart Instrument Co., Succasunna, N.J.). Advancing
(.theta..sub.adv) and receding (.theta..sub.rec) angles were
measured as water was supplied via a syringe into or out of sessile
droplets (drop volume.about.5 .mu.L). Measurements were taken at 2
different spots on each surface, and the reported measurements are
the averages of the four values for each sample (a left-side and
right-side measurement for each drop).
[0157] Contact angles were also evaluated in the same manner using
a 90/10 by wt. mixture of water/butoxyethanol instead of water.
Test Method 1 for Paint Repellency Evaluation
[0158] Test surfaces were submerged in the PPG Envirobase paint and
allowed to sit overnight. The test substrates were then removed
from the paint and held vertically for 5 min to allow the paint to
potentially flow off of the coating. The fraction (expressed as a
percentage) of the surface that was still covered by paint was
estimated by visual inspection.
Test Method 2 for Paint Repellency Evaluation--
[0159] Sample components or pieces thereof measuring approximately
4 cm.times.4 cm having a liquid repellent surface can be prepared
as described below and the initial masses measured. The PPG
Envirobase paint was pipetted onto these film pieces until the
entire surface was covered with paint. The painted film samples
were then turned vertically for 5 minutes to allow paint to drain
off of the surface. The masses of the drained film pieces were
measured to determine the mass of paint residue remaining on the
surface. The drained pieces were also visually inspected to
estimate the fraction (expressed as a percentage) of the film
surface that remains coated by the paint.
Test Method 3 for Paint Repellency Evaluation:
[0160] 70 g of PPG Envirobase automotive paint was poured into the
liner having the repellent interior surface and a comparative liner
(CE. F) that was the same liner without the repellent interior
surface. The liners were manually shaken and rotated to ensure that
the paint contacted all of the container side walls. The paint was
then poured out of the liners, and the liners were placed upside
down for 5 minutes (liner with repellent interior) or other
specified period of time to allow more of the paint to drain. The
liners were each reweighed and the mass of retained paint was
calculated.
Test Method 4 for Paint Repellency Evaluation:
[0161] A single drop of the (e.g. PPG Envirobase) paint,
approximately 0.2 mL, was applied at 21.degree. C. to a central
portion of the (e.g. repellent surface of the) sample (7.5 cm by
5.0 cm coated glass microscope slide). The sample (e.g. glass
slide) was immediately orientated vertically. If the paint drop
slid down the glass slide, it was denoted "Pass", if not "Fail". In
some samples that passed, a thin strip of paint (<20% the
thickness of the initial drop) or a few small droplets of paint
remained on the surface after the paint drop slid down.
Test Method 5 for Paint Repellency Evaluation:
[0162] The entire non-repellent surface of the sample (i.e.
uncoated side of the 7.5 cm by 5.0 cm glass slide) was masked with
tape, obtained from 3M Company under the trade designation
"SCOTCHBLUE PAINTERS TAPE". The sample (glass slide) was then
immersed in the (e.g. PPG Envirobase) paint to a depth of 3.5 cm
for 10 minutes at 21.degree. C. (or in other words about half the
coated surface was immersed). The sample (glass slide) was removed
from the diluted paint, orientated vertically for 30 seconds, and
the masking tape removed. The paint remaining on the immersed
coated surface was then visually estimated and expressed as
percentage of retained paint coverage.
Test Method 6 for Paint Repellency Evaluation:
[0163] A sample of sufficient size (2.8 by 3.2 cm) was weighed. The
entire non-repellent surface of the sample (i.e. uncoated side) was
masked with "SCOTCHBLUE PAINTERS TAPE". The repellent surface of
the sample was entirely submerged (e.g. 30 g) in the (e.g. PPG
Envirobase) paint for 10 minutes at 21.degree. C. The sample was
then removed from the paint, the masking tape removed, and the
sample orientated vertically by means a binder clip for 1 minute.
The bottom edge of the sample was contacted with a paper towel to
wick away paint that may have pooled along the bottom edge of the
material. The weight of each sample was again measured and the
amount of paint remaining per area was calculated. The paint
remaining on the coated surface was visually estimated and
expressed as percentage of retained paint coverage.
[0164] Unless specified otherwise, the test paint for determining
paint repellency according to the test methods described herein was
PPG Envirobase automobile paint mixed to specification containing
90 weight % ENVIROBASE HIGH PERFORMANCE T409 DEEP BLACK and 10
weight % ENVIROBASE HIGH PERFORMANCE T494 PAINT THINNER, available
from PPG Industries, Pittsburgh Pa. or available from 3M, St. Paul,
Minn.
Example 100 (EX100)--Preparation of Film with Siloxane Melt
Additive
[0165] A siloxane melt additive (alkyl dimethicone) was synthesized
as described in Example 14 of U.S. Pat. No. 9,187,678, (SMA). The
alkyl dimethicone was compounded into NA217000 LDPE (Lyondell
Basell, Houston, Tex.) at a loading of 15 wt. % using a 25 mm twin
screw extruder held at 190.degree. C. The alkyl dimethicone was
delivered to the extruder as a liquid at 120.degree. C. by means of
a heated gear pump and transfer line. The masterbatch melt was
extruded through a stranding die into a chilled water bath and
pelletized at a rate of 13.6 Kg/hour.
[0166] These 15 wt. % alkyl dimethicone masterbatch pellets were
then admixed with NA217000 LDPE pellets at a ratio which yielded a
pellet mixture comprising 3 wt. % alkyl dimethicone in LDPE. This 3
wt % alkyl dimethicone mixture was extrusion coated sequentially
onto both sides of 2 mil thick PET film (primed on both sides, 3M
Company) using the following procedure. The pellet blend was fed,
via a single feed hopper, at a rate of 20 lbs/hr into an extruder
and die operating at a temperature of 500.degree. F. The composite
extrudate exited the drop die opening and traveled approximately 10
cm to a nip where the composite was contacted with the primed PET
and solidified through a two roll nip equipped with a rubber and a
steel roller. The alkyl dimethicone/LDPE layer contacted a smooth
chilled steel roll which was used to accelerate the solidification
of the layers. The line speed was 50 ft/min, yielding an extruded
layer thickness of 1 mil. The final film construction consisted of
a 2 mil thick PET film sandwiched between 1 mil thick layers
comprising 3 wt. % alkyl dimethicone in LDPE.
[0167] The paint repellency of EX100 was also evaluated according
to Test Method 2 as previously described. The results were as
follows:
TABLE-US-00001 Mass Paint on Percentage of Surface Example Surface
(g/cm.sup.2) Coated with Paint EX100 0.00074 5%
[0168] The paint repellency of EX100 was also evaluated according
to Test Method 6 as previously described using a 4 cm.times.4 cm
sample size. The results were as follows:
TABLE-US-00002 Mass Paint on Percentage of Surface Example Surface
(g/cm.sup.2) Coated with Paint EX100 0.0035 15%
Surface Abrasion Test
[0169] A sample of sufficient size (e.g., 6 cm by 2 cm) was
prepared and mounted on a Taber Abraser (Taber Industries 5750
Linear Abraser). A crockmeter square (AATC Crockmeter Square from
Testfabrics, Inc.) was attached to the abraser head by means of a
rubber band. No additional weights were placed on top of the
abraser head. The cycle speed was set to 15 cycles/min, and each
substrate was subjected to 2 abrasion cycles (or in other words the
abraser head passed back and forth twice).
[0170] Contact angles with a solution containing 10% by weight of
2-n-butoxyethanol and 90% by weight deionized water and paint
repellency were tested after being subjected to this surface
abrasion.
TABLE-US-00003 10% (by wt.) aqueous 2-n-butoxyethanol Contact
Angles After Abrasion Paint Repellency CAH After Abrasion Example
.theta..sub.adv .theta..sub.rec (.theta..sub.adv - .theta..sub.rec)
Test Method 4 EX100 53 45 8 Pass
[0171] The repellency of EX100 after abrasion was also evaluated by
measuring the contact angles with water as previously described.
The results were as follows:
TABLE-US-00004 Water Contact Angles After Abrasion CAH Example
.theta..sub.adv .theta..sub.rec (.theta..sub.adv - .theta..sub.rec)
EX100 109 99 10
[0172] The paint repellency of EX100 after abrasion was also
evaluated according to Test Method 2 with the PPG paint as
previously described, except 2.2 cm.times.3.2 cm substrates were
used in place of 4 cm.times.4 cm samples. The results were as
follows:
TABLE-US-00005 Mass Paint on Fraction of Surface Surface
(g/cm.sup.2) Coated with Paint Example After Abrasion After
Abrasion EX100 0.00040 <5%
[0173] The paint repellency of EX100 after abrasion were also
evaluated according to Test Method 6 with PPG paint as previously
described, except 2.2 cm.times.3.2 cm substrates were used in place
of 4 cm.times.4 cm samples. The results were as follows:
TABLE-US-00006 Mass Paint on Fraction of Surface Example Surface
(g/cm.sup.2) Coated with Paint EX100 0.0018 10%
Materials
TABLE-US-00007 [0174] Material Designation Description Obtained
from NA217000 NA217000 low density Lyondell Basell, LDPE
polyethylene Houston, TX Marflex 1122 Marflex 1122 low density
Chevron Phillips, The LDPE polyethylene Woodlands, TX butoxyethanol
2-n-butoxyethanol Alfa Aesar, Ward Hill, MA UHMW Siloxane Dow
Corning .RTM. MB50-002 Dow Corning, Midland, ultra high molecular
weight MI siloxane dispersed in low density polyethylene IPA
isopropanol BDH Chemicals/VWR, Radnor, PA NMP
n-methyl-2-pyrrolidone TCI America, Portland, OR Lexan .TM. 1414T
Lexan .TM. EXL1414T Saudi Arabia Basic polycarbonate-siloxane
Industries Corporation copolymer (SABIC), Riyadh, Saudi Arabia PPS
.TM. liners thermoformed low density 3M polyethylene (400 ml)
Preparation of Additional Examples with Siloxane Melt Additive
[0175] Two cast web films with an overall film thickness of
.about.40 mils--PE101 and PE102--were produced using the
SMA/NA217000 masterbatch. Both films comprised 3 layers of
approximately equal thicknesses (.about.13.3 mils per layer, total
thickness about 40 mils). For PE101, all layers were produced by
mixing pellets of the aforementioned masterbatch with pellets of
NA217000 LDPE such that the composition of each layer comprised
97/3 (by wt) NA217000/SMA. The outer (A or air-side) layer was
produced by extruding the 97/3 LDPE/SMA mixture through a 27 mm
twin screw extruder through a neck tube and gear pump into the top
layer of the 3 layer feed block and die. This melt train used a
progressive temperature extrusion profile, with peak temperatures
of .about.250.degree. C. The middle (B) layer was produced by
extruding the 97/3 LDPE/SMA mixture through a 27 mm twin screw
extruder with a progressive temperature profile peaking at or
around 275-280.degree. C. through a neck tube and gear pump into
the middle layer of the feed block and die. The bottom (C or wheel
side) layer was produced by extruding the 97/3 LDPE/SMA mixture
through a 25 mm twin screw extruder through a neck tube and gear
pump into the bottom layer of the feed block and die. Once again, a
progressive temp profile was used with peak temperatures of 280 to
285.degree. C. The feedblock/die was held at a target temp of 270
to 275.degree. C. while the casting wheel was run at about
80-85.degree. C. Film PE102 was made using essentially identical
processing conditions as PE101, except the composition varied from
layer to layer in this sample. The air-side (A) and middle (B)
layers comprised Marflex 1122 LDPE, whilst the wheel side (C) layer
comprised a mixture of NA217000/SMA masterbatch and Marflex 1122
such that the C layer composition was 85/12/3 (by wt) Marflex
1122/NA217000/SMA.
[0176] Both of the 40 mil thick film samples were thermoformed into
400 ml PPS.TM. liners, summarized as follows:
TABLE-US-00008 SMA Example Loading Sample Description CE1 0
commercial 400 mL PPS .TM. liner EX101 3 wt. % 3 wt. % SMA in
NA217000 LDPE EX102 3 wt. % 3 wt. % SMA in NA217000 LDPE/ in `skin`
Marflex 1122 LDPE `skin,` backed by Marflex 1122 LDPE
[0177] A polycarbonate-siloxane copolymer coating was prepared by
dissolving 2.5 wt.-% of the indicated polymer in solvent as
described below.
TABLE-US-00009 Wt. % Polycarbonate- Solvent Siloxane
Polycarbonate-Siloxane Polymer(s) Coating 1 - 80/20 2.5 Lexan .TM.
1414T NMP/IPA
[0178] To prepare Example EX103, the coating solution was applied
to the inside walls of the spray gun paint container using a
pipette as follows: the bottom of a LDPE PPS.TM. container was
first wet with the coating solution, and the solvent was allowed to
evaporate under ambient conditions. The container was then tilted
90.degree. and a pipette was used to coat a strip of the interior
side wall of the container. Next, the container was manually
rotated to obtain complete wetting of the entire interior sidewall
by the coating solution. Excess coating solution was drained by
flipping the container upside down, and the solvent was allowed to
evaporate in an oven at 80.degree. C. for 15 minutes (polyethylene
liners). Paint repellency was determined according to Test Method 3
as follows:
[0179] Paint containers or spray application system coated with
polycarbonate-siloxane materials.
TABLE-US-00010 Coating Identity of Polycarbonate- Example Base
Container Material Siloxane Polymer(s) EX103 400 mL Coating 1 Lexan
.TM. 1414T polyethylene liner
The paint repellency of the aforementioned containers having the
repellent interior surfaces and comparative containers was
evaluated according to Test Method 3 as previously described. The
mass of the containers was also measured after 5, 90, and 180
minutes. Paint repellency of sample paint containers as quantified
using Test Method 3.
TABLE-US-00011 Mass Mass of Paint Retention Mass Per Empty
Following Drainage Time Surface Area Liner Specified in Row Below
(g) Calculation Example (g) 5 min 90 min 180 min (at t = 90 min,
g/cm.sup.2) CE1 5.89 8.72 4.28 3.39 0.015 EX101 5.86 3.53 0.84 0.44
0.004 (80% less paint retained*) EX102 5.48 7.61 1.67 1.05 0.006
(61% less paint retained) EX103 5.83 8.14 1.64 0.54 0.006 (62% less
paint retained) *(4.28 - 0.84)/4.28 .times. 100%
Preparation of LDPE/Ultra High Molecular Weight (UHMW) Siloxane
Film (EX104).
[0180] A film comprising 97.5/2.5 (by wt) LDPE/UHMW siloxane was
produced by adding 9.5 g LDPE (Chevron Phillips Marflex 1122) and
0.5 g of UHMW siloxane masterbatch (Dow Corning MB 50-002; 50/50 by
wt siloxane/LDPE pellets) into a DSM compounder (DSM Xplore Micro
15 cc Twin Screw Compounder). The compounder was held constant at
170.degree. C. and the screw speed was set to 40 rpm/10,000 N.
After allowing the melted resin to recirculate and mix in the
compounder for 10 minutes, the melt was extruded through a slotted
die and the resultant 28 mm wide, 0.1-0.2 mm thick film was wound
onto a 3'' fiber core.
Fluid Contact Angles and Paint Repellency of Various Test
Surfaces
[0181] Pieces were cut from the sides of a commercially available
400 mL PPS.TM. liner, from the sides of the thermoformed
SMA-containing liners (EX101 and EX102), from the sides of the
polycarbonate-siloxane coated LDPE liners (EX103), and from the
roll of LDPE/UHMW Siloxane (EX104). These cut pieces of film were
used for contact angle testing with water and with a solution
containing 10% by weight of 2-n-butoxyethanol and 90% by weight
deionized water instead of deionized water. The measured contact
angle data for these samples are provided below, along with the
characterization data for these samples using Paint Repellency Test
Method 4.
TABLE-US-00012 10% (by wt.) aqueous 2-n-butoxyethanol Water Contact
Angles Contact Angles CAH CAH Paint Exam- (.theta..sub.adv -
(.theta..sub.adv - Repellency ple .theta..sub.adv .theta..sub.rec
.theta..sub.rec) .theta..sub.adv .theta..sub.rec .theta..sub.rec)
Test Method 4 CE1 105 95 10 51 21 30 Fail EX101 111 95 16 54 46 8
Pass EX102 111 99 12 55 46 9 Pass EX103 107 99 8 54 45 9 Pass EX104
116 87 29 60 40 20 Pass
[0182] Paint Repellency was also evaluated according to Test Method
2
TABLE-US-00013 Mass Paint on Fraction of Surface Example Surface
(g/cm.sup.2) Coated with Paint CE1 0.022 ~95% EX101 0.004 ~15%
EX102 0.006 ~10% EX103 0.006 ~20% EX104 0.003 ~25%
[0183] Paint Repellency was also evaluated according to Test Method
6 as previously described using a 4 cm.times.4 cm sample size.
TABLE-US-00014 Mass Paint on Fraction of Surface Example Surface
(g/cm.sup.2) Coated with Paint CE1 0.022 ~95% EX101 0.004 ~15%
EX102 0.006 ~20% EX103 0.007 ~25% EX104 0.013 ~60%
[0184] The test surfaces EX1-EX3 and EX5 were subjected to the
Surface Abrasion Test. Contact angles with a solution containing
10% by weight of 2-n-butoxyethanol and 90% by weight deionized
water and paint repellency as quantified by Test Method 4 were
measured after each test substrate was subjected to this surface
abrasion.
TABLE-US-00015 10% (by wt.) aqueous 2-n-butoxyethanol Contact
Angles After Abrasion Paint Repellency CAH Test Method 4 Example
.theta..sub.adv .theta..sub.rec (.theta..sub.adv - .theta..sub.rec)
After Abrasion EX101 54 44 10 Pass EX102 53 44 9 Pass EX103 50 43 7
Pass EX104 63 38 25 Pass
[0185] The repellency after abrasion were also evaluated by
measuring the contact angles with water as previously described.
The results were as follows:
TABLE-US-00016 Water Contact Angles After Abrasion CAH Example
.theta..sub.adv .theta..sub.rec (.theta..sub.adv - .theta..sub.rec)
EX101 108 92 16 EX102 112 96 16 EX103 106 93 13 EX104 111 81 30
[0186] Paint Repellency was also evaluated according to Test Method
2, except 2.2 cm.times.3.2 cm sized samples were used in place of 4
cm.times.4 cm samples.
TABLE-US-00017 Mass Paint on Fraction of Surface Surface
(g/cm.sup.2) Coated with Paint Example After Abrasion After
Abrasion EX101 0.003 ~5% EX102 0.003 ~10% EX103 0.002 ~5% EX104
0.005 ~20%
Panel Painting Using Base Coats which had Contacted
Siloxane-Functional Materials
[0187] Two types of experiments were done to ascertain whether
"fish-eyeing" is problematic when waterborne base coats contact the
siloxane-functional surfaces described herein. The first type of
experiment involved pouring a ready-to-spray paint mixture into the
repellent containers of EX101-EX103. The "ready-to-spray" mixture
contained 88 wt. % of ENVIROBASE HIGH PERFORMANCE T407 JET BLACK
and 12 weight % ENVIROBASE HIGH PERFORMANCE T494 PAINT THINNER,
available from PPG Industries.
[0188] These repellent containers were used in conjunction with
industry-standard spray application equipment to spray PPG
Envirobase paint. Once this base coat was dry, a coat of clearcoat
was applied to the panel (the clearcoat was obtained from PPG
Industries, Inc. as the trade designation EC530 PERFORMANCE
CLEARCLOAT). The paint could be uniformly applied at a sufficient
film build. There was no evidence of "fisheyes" or other
incompatibility-related coating defects while applying the paint
and/or by uneven gloss and/or color.
[0189] The second type of experiment was completed with the UHMW
siloxane material. In this experiment, 6.3 g of the MB50-002 resin
pellets obtained from Dow-Corning (siloxane content of 50%) and 50
g the ready-to-spray paint mixture were mixed in a commercial 400
mL PPS.TM. liner. The pellets were soaked in the Envirobase at room
temperature for 7 days, at which point the Envirobase base coat and
EC530 clearcoat were sprayed onto an automotive panel as described
above. The paint could be uniformly applied at a sufficient film
build, and there was no evidence of "fisheyes" or other
incompatibility-related coating defects while applying the paint
and/or by uneven gloss and/or color.
[0190] Some additional test liquids were utilized to evaluated
liquid repellency using Test Method 2. The length of time the
sample film was held vertically to allow the liquid to drain in
indicated. The test results are as follows:
TABLE-US-00018 Results for CE1 Results for EX101 (LDPE) (97/3
LDPE/SMA) Average Average Average % of Average % of Retained
Surface Retained Surface Mass (mg) Covered Mass (mg) Covered Test
Liquid (g/cm.sup.2) by Fluid (g/cm.sup.2) by Fluid Poly(propylene
glycol), 70.7 75 15.5 5 400 Mw (Polysciences (0.0044) (0.00097)
Inc., Warrington, PA) - 30 minutes Butoxyethanol (100%) - (0.0019)
100 (0.00094) 1 0.5 ml applied and a 30 second drain time Solution
of 50 wt. (0.0018 95 (0.000163 5 % butoxyethanol and 50 wt. % water
- 0.5 ml applied and a 30 second drain time
* * * * *