U.S. patent application number 15/321299 was filed with the patent office on 2017-12-14 for silicone release coating composition and low release force emulsion silicone release coating for films and papers having cured release coating.
The applicant listed for this patent is Dow Corning (China) Holding Co., Ltd., Dow Corning Corporation. Invention is credited to Fuming HUANG, Chung Mien KUO, Yang WANG.
Application Number | 20170355878 15/321299 |
Document ID | / |
Family ID | 54936501 |
Filed Date | 2017-12-14 |
United States Patent
Application |
20170355878 |
Kind Code |
A9 |
HUANG; Fuming ; et
al. |
December 14, 2017 |
SILICONE RELEASE COATING COMPOSITION AND LOW RELEASE FORCE EMULSION
SILICONE RELEASE COATING FOR FILMS AND PAPERS HAVING CURED RELEASE
COATING
Abstract
A silicone release coating composition comprises: (A) 100 weight
parts of an organopolysiloxane fluid having a viscosity at
25.degree. C. of 50 to 10,000 mPas and an alkenyl content of 0.10
to 3.0 wt %; (B) 0.5-40 weight parts of a diorganopolysiloxane
represented by the average structural formula (1):
R.sup.c.sub.3SiO(R.sup.bR.sup.cSiO.sub.2/2).sub.n1(R.sup.c.sub.2SiO.sub.-
2/2).sub.n2SiR.sup.c.sub.3 (1) wherein R.sup.b is an alkenyl group;
R.sup.c is an alkyl group or a phenyl group; n1 provides an alkenyl
content of 0.05 to 0.80 wt. %; n2 is at least 1; and n1+n2 provides
this component with a viscosity at 25.degree. C. of 5,000 to
150,000 mPas; (C) an organohydrogenpolysiloxane that has a
viscosity at 25.degree. C. of 1 to 1,000 mPas, at least two
silicon-bonded hydrogen atoms in each molecule, and an alkyl group
or a phenyl group for its silicon-bonded organic groups; (D) a
hydrosilylation reaction catalyst in a catalytic amount; (E) a
surfactant; (F) water; and (G) an inhibitor.
Inventors: |
HUANG; Fuming; (Shanghai,
CN) ; KUO; Chung Mien; (Chungli, TW) ; WANG;
Yang; (Shanghai, CN) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Dow Corning Corporation
Dow Corning (China) Holding Co., Ltd. |
Midland
Shanghai |
MI |
US
CN |
|
|
Prior
Publication: |
|
Document Identifier |
Publication Date |
|
US 20170145256 A1 |
May 25, 2017 |
|
|
Family ID: |
54936501 |
Appl. No.: |
15/321299 |
Filed: |
June 27, 2014 |
PCT Filed: |
June 27, 2014 |
PCT NO: |
PCT/CN2014/080924 PCKC 00 |
371 Date: |
December 22, 2016 |
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
D21H 19/12 20130101;
C09D 183/04 20130101; C09D 5/022 20130101; C08L 83/00 20130101;
C08K 5/56 20130101; C08G 77/12 20130101; C08L 83/00 20130101; C08G
77/20 20130101; C08G 77/80 20130101; C09D 183/04 20130101 |
International
Class: |
C09D 183/04 20060101
C09D183/04; D21H 19/12 20060101 D21H019/12; C09D 5/02 20060101
C09D005/02 |
Claims
1. A silicone release coating composition comprising: (A) 100
weight parts of an organopolysiloxane fluid having a viscosity at
25.degree. C. of 50 to 10,000 mPas and an alkenyl content of 0.10
to 3.0 wt %; (B) 0.5-40 weight parts of a diorganopolysiloxane
represented by the average structural formula (1):
R.sup.c.sub.3SiO(R.sup.bR.sup.cSiO.sub.2/2).sub.n1(R.sup.c.sub.2SiO.sub.2-
/2).sub.n2SiR.sup.c.sub.3 (1) wherein R.sup.b is alkenyl group
having 2 to 8 carbon atoms; R.sup.c is alkyl group having 1 to 8
carbon atoms or a phenyl group; n1 provides an alkenyl content of
0.05 to 0.80 wt %; n2 is at least 1; and n1+n2 provides this
component with a viscosity at 25.degree. C. of 5,000 to 150,000
mPas; (C) an organohydrogenpolysiloxane that has a viscosity at
25.degree. C. of 1 to 1,000 mPas, at least two silicon-bonded
hydrogen atoms in each molecule, and an alkyl group having 1 to 8
carbon atoms or a phenyl group for its silicon-bonded organic
groups, in an amount sufficient to provide a value of 0.8:1 to 5:1
for the molar ratio of silicon-bonded hydrogen atoms in this
component to the alkenyl groups in components (A) and (B); (D) a
hydrosilylation reaction catalyst in a catalytic amount; (E) a
surfactant; (F) water; and (G) an inhibitor.
2. The silicone release coating composition according to claim 1,
wherein the alkenyl content of component (B) is within a range of
0.05 to 0.50 wt %.
3. The silicone release coating composition according to claim 1,
wherein component (A) is 100 weight parts of at least one
organopolysiloxane fluid selected from the group consisting of: a
linear organopolysliloxane, a branched organopolysiloxane, a
mixture of organopolysiloxanes having different alkenyl contents of
0.10 to 3.0 wt %, and a mixture of a linear organopolysliloxane and
a branched organopolysiloxane.
4. The silicone release coating composition according to claim 1,
wherein component (A) is a mixture of (A-1) a polydimethylsiloxane
having alkenyl groups only in its molecular terminals and (A-2) a
polydimethylsiloxane having alkenyl groups in its molecular
terminals and its side-chain positions.
5. The silicone release coating composition according to claim 1,
wherein component (A) comprises at least one organopolysiloxane
fluid having a branched structure and a viscosity at 25.degree. C.
of 50 to 10,000 mPas, comprising the siloxane units (i) to (iii)
described below, and having a straight-chain moiety comprising a
plurality of siloxane unit (ii), and a branch point comprising
siloxane unit (i), wherein the terminals of the straight-chain
moiety are end blocked by the siloxane unit (iii); (i) the siloxane
unit represented by the general formula SiO.sub.4/2: 1 or more;
(ii) the siloxane unit represented by the general formula
R.sub.2SiO.sub.2/2: 15 to 995; (iii) the siloxane unit represented
by the general formula R.sup.aR.sub.2SiO.sub.1/2; in the formulae,
R.sup.a is selected from the group consisting of alkyl groups
having 1 to 8 carbon atoms, alkenyl groups having 2 to 8 carbon
atoms, a phenyl group, alkoxy groups having 1 to 8 carbon atoms,
and a hydroxyl group, and R is selected from the group consisting
of alkyl groups having 1 to 8 carbon atoms, alkenyl groups having 2
to 8 carbon atoms, and a phenyl group, wherein at least 0.10 to 3.0
wt % of the R.sup.a and R in the molecule are alkenyl groups having
2 to 8 carbon atoms and at least 50% of the total number of R.sup.a
and R in the molecule are alkyl groups having 1 to 8 carbon
atoms.
6. The silicone release coating composition according to claim 5,
wherein component (A) comprises at least one organopolysiloxane
fluid having a branched structure and represented by the average
siloxane unit formula (2):
(R.sup.aR.sub.2SiO.sub.1/2).sub.4(R.sub.2SiO.sub.2/2).sub.m(SiO.sub-
.4/2) (2) wherein R.sup.a is selected from the group consisting of
alkyl groups having 1 to 8 carbon atoms, alkenyl groups having 2 to
8 carbon atoms, a phenyl group, alkoxy groups having 1 to 8 carbon
atoms, and a hydroxyl group; R is selected from the group
consisting of alkyl groups having 1 to 8 carbon atoms, alkenyl
groups having 2 to 8 carbon atoms, and a phenyl group; at least 3
wt % of the R.sup.a and R in the molecule are alkenyl groups having
2 to 8 carbon atoms; at least 50% of the total number of R.sup.a
and R in the molecule are alkyl groups having 1 to 8 carbon atoms;
and m=15 to 995.
7. The silicone release coating composition according to claim 5,
wherein component (A) is an organopolysiloxane having a branched
structure and represented by the average siloxane unit formula (3):
[(R.sup.bR.sup.c.sub.2SiO.sub.1/2).sub.n(R.sup.dR.sup.c.sub.2SiO.sub.1/2)-
.sub.1-n].sub.4(R.sup.bR.sup.cSiO.sub.2/2).sub.m1(R.sup.c.sub.2SiO.sub.2/2-
).sub.m2(SiO.sub.4/2) (3) wherein R.sup.b is an alkenyl group
having 2 to 8 carbon atoms; R.sup.c is an alkyl group having 1 to 8
carbon atoms or a phenyl group; R.sup.d is selected from the group
consisting of alkyl groups having 1 to 8 carbon atoms, alkoxy
groups having 1 to 8 carbon atoms, and a hydroxyl group; there are
at least three R.sup.b in the molecule; at least 50% of the total
number of R.sup.b, R.sup.c, and R.sup.d in the molecule are alkyl
groups having 1 to 8 carbon atoms; n is 0 or 1; m1 is at least 1;
m2 is at least 0; and m1+m2=15 to 995.
8. The silicone release coating composition according to claim 1,
wherein component (E) comprises at least one nonionic surfactant
selected from the group consisting of polyether compounds,
polyether-modified silicones, water-soluble polyester compounds,
water-soluble polyvinyl alcohols and water-soluble
polyvinylacetates.
9. The silicone release coating composition according to claim 1,
wherein component (G) is a hydrosilylation reaction inhibitor, is
noncuring at ambient temperature, and cures under the application
of heat.
10. A low release force emulsion silicone release coating for films
and papers yielded by curing the silicone release coating
composition according to claim 1.
11. A production method of a low release force emulsion silicone
release coating for films and papers, said method comprising:
applying the silicone release coating composition according to
claim 1 on at least one side of a film or a paper; and curing the
applied coating at a temperature of at least 100.degree. C.
12. The silicone release coating composition according to claim 1,
wherein component (E) comprises an ethoxylated alcohol or a
polyoxyethylene alkyl ether.
13. The silicone release coating composition according to claim 12,
wherein component (E) further comprises a polyvinyl alcohol.
14. The silicone release coating composition according to claim 1,
wherein component (E) is present in an amount of from 0.5 to 30
weight parts per 100 weight parts of component (A).
15. The silicone release coating composition according to claim 1,
wherein component (F) is present in an amount of from 60 to 2000
weight parts per 100 weight parts of component (A).
16. The silicone release coating composition according to claim 1,
wherein component (G) is present in an amount of from 0.05 to 2
weight parts per 100 weight parts of component (A).
Description
TECHNICAL FIELD
[0001] The present invention relates to an emulsion composition for
the silicone release coating application. The release coating
composition is applied to coat a layer on films or paper substrate
and cured under thermal addition to form a coated substrate. The
invention is intent to provide a coated release liner with low
release force for tape release, sticky adhesive or label release
application. In particular, the present invention relates to a
silicone release coating composition, a low release force emulsion
silicone release coating for films and papers yielded by curing the
silicone release coating composition, and a production method of a
low release force emulsion silicone release coating for films and
papers.
BACKGROUND ART
[0002] Conventionally, an emulsion (EM) type silicone release
coating has short chain vinyl-end silicone polymers or multiple
vinyl functional silicone polymers to get fast cure with acceptable
migration and also easy to be emulsified, so the base polymers have
to be low viscosity to meet the manufacture process requirement.
The coating is, however, difficult to provide low release force due
to high cure density.
[0003] For example, U.S. Pat. No. 4,791,029A (Patent Reference 1,
incorporated herein for reference) discloses aqueous emulsions of
crosslinkable polyaddition organopolysiloxane compositions,
comprising: a first aqueous emulsion A including end-vinylated
polysiloxanes, a vinylated cyclotrisiloxane, a
hydroorganodiorganopolysiloxane, a polyvinyl alcohol and a
polyalkylene glycol alkyl ether or alkylphenyl ether, and a second
aqueous emulsion B which comprises a catalytically effective amount
of a platinum metal catalyst with siloxane polymer. The emulsions
are said to be well adapted for the thin layer coating of flexible
substrates to impart water-repellency and nonadherency thereto.
[0004] For example, U.S. Pat. No. 4,954,554A (Patent Reference 2,
incorporated herein for reference) discloses aqueous emulsions of
curable silicone compositions which provide cured coatings having
improved gloss and/or water-repellancy and/or adhesive release if
formulated to contain polyvinylachohol (PVA) having a degree of
hydrolysis of 90 mol. % or more. The extent of improvement is
directly related to the degree of hydrolysis of the PVA. PVA having
an average degree of hydrolysis of from 94 to 99 mol. % is
particularly effective for improving these properties of cured
coatings. Conveniently, a mixture of two or more commercially
available PVAs having different degrees of hydrolysis can be used
to arrive at a PVA having a desired degree of hydrolysis.
[0005] For example, U.S. Pat. No. 5,095,067A (Patent Reference 3,
incorporated herein for reference) discloses a release silicone
emulsion composition comprising: (A) 100 parts by weight of a
specific organovinylpolysiloxane; (B) from 1 to 50 parts by weight
of a specific organohydrogenpolysiloxane; (C) from 0.5 part to 5
parts by weight of a platinum catalyst having a viscosity of 10 cSt
or less at 25.degree. C.; (D) from 1.5 to 15 parts by weight of a
nonionic emulsifying agent having an average HLB of from 10 to 20,
pH of 6.5 or less and an ionic conductance of 30 .mu.S/cm or less;
and (E) water. This composition is said to have good pot life and
curability. The cured film had good release properties and residual
adhesive properties of adhesives.
[0006] For example, U.S. Pat. No. 5,777,017A (Patent Reference 4,
incorporated herein for reference) discloses aqueous
organopolysiloxane emulsions, especially those which can be
crosslinked by addition of Si-bonded hydrogen onto aliphatic
multiple bond, their preparation with an emulsifier combination
comprising alkylphenyl polyglycol ether and polyvinyl alcohol with
a low degree of hydrolysis, and their use for preparing
anti-adhesive coatings.
[0007] For example, US 20110287267A1 (Patent Reference 5,
incorporated herein for reference) discloses a solventless cured
release coating-forming organopolysiloxane composition having a
viscosity at 25.degree. C. of 50 to 2,000 mPas comprising (A) 100
weight parts of an alkenyl-functional diorganopolysiloxane that has
a viscosity of 25 to 1,000 mPas; (B) 0.5 to 15 weight parts of a
diorganopolysiloxane that has a viscosity of at least 10,000 mPas
and that has an aliphatically unsaturated group content of no more
than 0.1 mole %; (C) 0.5 to 5 weight parts of a branched
organopolysiloxane that has more than one SiO.sub.4/2 unit and that
is a polymer product provided by an equilibration polymerization
between a branched organosiloxane oligomer represented by the
average siloxane unit formula (1)
(SiO.sub.4/2)(R.sup.aR.sup.b.sub.2SiO.sub.1/2).sub.x and a
diorganosiloxane oligomer; (D) a specific amount of an
organohydrogenpolysiloxane that has a viscosity of 1 to 1, 000
mPas; and (E) a hydrosilylation reaction catalyst in a catalytic
quantity. The resulting cured coating is said to exhibit an
excellent release performance to tacky substances and a smooth
slipperiness.
[0008] For example, U.S. Pat. No. 4,870,149A (Patent Reference 6,
incorporated herein for reference) discloses a solventless, cured
release coating-forming organopolysiloxane composition comprising
(A) 100 parts of an organopolysiloxane fluid having a branched
structure and comprising (i) the siloxane unit represented by the
formula SiO.sub.4/2, (ii) the siloxane unit represented by the
general formula R.sub.2SiO.sub.2/2, and (iii) the siloxane unit
represented by the general formula RaR.sub.2SiO.sub.1/2; (B) 0.5 to
15 parts of a diorganopolysiloxane with the average structural
formula
R.sup.aR.sup.c.sub.2SiO(R.sup.bR.sup.cSiO.sub.2/2).sub.n1(R.sup.c.sub.2Si-
O.sub.2/2).sub.n2SiR.sup.c.sub.2R.sup.a; (C) a prescribed quantity
of an organohydrogenpolysiloxane; and (D) a hydrosilylation
reaction catalyst. Also, a sheet-form substrate has a cured coating
from this solventless, cured release coating-forming
organopolysiloxane composition.
[0009] However, the above Patent References 1-6 fail to well solve
the above technical problem of the prior art. Particularly, Patent
References 1-4, which relate to aqueous emulsions, cannot provide a
low release force emulsion silicone release coating; and Patent
References 5-6, which relate to solventless, cured release
coating-forming organopolysiloxane composition, obviously cannot
meet the requirement on aqueous emulsions.
[0010] Therefore, there still exists a need in the art for
obtaining an aqueous emulsion type silicone release coating
composition which can provide a lower release force at same coat
weight (CW) to sticky adhesive and possessing excellent properties
including high-speed cure, cured layer with low migration, slippery
& good smooth touch of the coating surface, and good anchorage
to the substrate.
SUMMARY OF THE INVENTION
[0011] The present invention was pursued in order to solve the
problems cited above and has as an object the introduction of a low
release force emulsion silicone release coating application. The
release coating composition is applied to coat a layer on films or
paper substrate and cured under thermal addition to form a coated
substrate. Another object of the present invention is to provide a
coated release liner with low release force for tape release,
sticky adhesive or label release application.
[0012] To overcome the above existing defect, this invention
discloses a cured release coating using a certain long chain
polysiloxane additive. The additive has high viscosity (5,000 to
150,000 cp) and reactive vinyl functional group, which vinyl
functional group pendant on side chain is easily form covalently
bonded by hydrosliation with SiH function crosslinker. The
terminated group of siloxane additive has no reactive. This
invention discloses a silicone release coating composition,
comprises: (I) silicone compound comprising vinyl pendant silicone
additive for lower release force on a polymer film substrate or
paper, wherein the additive is vinyl functional group pendant on
side chain with non-reactive group terminated; (II) an
organohydrogenpolysiloxane cross-linking agent in an amount such
that the ratio of the total number of silicon hydride (Si-H) groups
in (II) to aliphatically unsaturated hydrocarbon groups in (I) is
from 0.9:1 to 3:1; (III) a sufficient amount of a hydrosilylation
catalyst effective to catalyze the reaction between the vinyl
siloxane and the cross-linking agent; (IV) surfactants; (V) water;
and (VI) inhibitor.
[0013] Through compounding of silicone base and additive, the
additive together with base polymer form a part cured network on
substrate that can provide a lower release force to sticky
adhesive. The viscosity of the mixture maintains a reasonable base
viscosity suitable for emulsification. The other properties of
coating liner keeps as good as base polymer in performance of
anchorage testing like Rub Off (RO), delayed RO, Subsequent
Adhesive Strength (SAS) and Extractable.
DISCLOSURE OF THE INVENTION
[0014] The objects cited above can be achieved by the following:
[0015] {1} A silicone release coating composition, comprising:
[0016] (A) 100 weight parts of an organopolysiloxane fluid having a
viscosity at 25.degree. C. of 50 to 10,000 mPas and alkenyl content
of 0.10 to 3.0 wt %; [0017] (B) 0.5-40 weight parts of a
diorganopolysiloxane represented by the average structural formula
(1), having a viscosity at 25.degree. C. of 5,000 to 150,000 mPas
and alkenyl content of 0.05 to 0.80 wt. %:
[0017]
R.sup.c.sub.3SiO(R.sup.bR.sup.cSiO.sub.2/2).sub.n1(R.sup.c.sub.2S-
IO.sub.2/2).sub.n2SiR.sup.c.sub.3 (1)
wherein R.sup.b is alkenyl having 2 to 8 carbon atoms; R.sup.c is
alkyl group having 1 to 8 carbon atoms or phenyl; n1 is a number
that provides alkenyl content of 0.05 to 0.80 wt %; n2 is a number
with a value of at least 1; and n1+n2 is a number that provides
this component with a viscosity at 25.degree. C. of 5,000 to
150,000 mPas; [0018] (C) an organohydrogenpolysiloxane that has a
viscosity at 25.degree. C. of 1 to 1,000 mPas and that has at least
two silicon-bonded hydrogen atoms in each molecule, and has alkyl
group having 1 to 8 carbon atoms or phenyl group for its
silicon-bonded organic groups, in an amount sufficient to provide a
value of 0.8:1 to 5:1 for the molar ratio of silicon-bonded
hydrogen atoms in this organohydrogenpolysiloxane to the alkenyl
groups in components (A) and (B); [0019] (D) a hydrosilylation
reaction catalyst in a catalytic amount; [0020] (E) surfactant,
[0021] (F) water; and [0022] (G) inhibitor. [0023] {2} The silicone
release coating composition according to {1}, characterized in that
alkenyl content of component (B) is preferable within a range of
0.05 to 0.50wt %. [0024] {3} The silicone release coating
composition according to {1}, characterized in that component (A)
is 100 weight parts of at least one organopolysiloxane fluid
selected from the group consists of: linear organopolysliloxane,
branched organopolysiloxane, mixture of organopolysiloxanes having
different alkenyl contents of 0.10 to 3.0 wt %, and mixture of
linear organopolysliloxane and branched organopolysiloxane. [0025]
{4} The silicone release coating composition according to {1},
characterized in that component (A) is a mixture of (A-1)
polydimethylsiloxane having alkenyl groups only in its molecular
terminals and (A-2) polydimethylsiloxane having alkenyl groups in
its molecular terminals and its side-chain positions. [0026] {5}
The silicone release coating composition according to {1},
characterized in that component (A) comprises at least one
organopolysiloxane fluid having a branched structure and a
viscosity at 25.degree. C. of 50 to 10,000 mPas, comprising the
siloxane units (i) to (iii) described below, and having a
straight-chain moiety comprising a plurality of siloxane unit
(ii)'s, and a branch point comprising siloxane unit (i), wherein
the terminals of the straight-chain moiety are end blocked by the
siloxane unit (iii) [0027] (i) the siloxane unit represented by the
general formula SiO.sub.4/2: 1 or more [0028] (ii) the siloxane
unit represented by the general formula R.sub.2SiO.sub.2/2: 15 to
995 [0029] (iii) the siloxane unit represented by the general
formula R.sup.aR.sub.2SiO.sub.1/2
[0030] in the formulae, R.sup.a is a group selected from the group
consisting of alkyl having 1 to 8 carbon atoms, alkenyl having 2 to
8 carbon atoms, phenyl, alkoxy having 1 to 8 carbon atoms, and the
hydroxyl group, and R is a group selected from the group consisting
of alkyl having 1 to 8 carbon atoms, alkenyl having 2 to 8 carbon
atoms, and phenyl, wherein at least 0.10 to 3.0 wt % of the R.sup.a
and R in the molecule are alkenyl group having 2 to 8 carbon atoms
and at least 50% of the total number of R.sup.a and R in the
molecule is alkyl group having 1 to 8 carbon atoms. [0031] {6} The
silicone release coating composition according to {5},
characterized in that component (A) comprises at least one
organopolysiloxane fluid having a branched structure and
represented by the average siloxane unit formula (2):
[0031]
(R.sup.aR.sub.2SiO.sub.1/2).sub.4(R.sub.2SiO.sub.2/2).sub.m(SiO.s-
ub.4/2) (2)
wherein R.sup.a is a group selected from the group consisting of
alkyl having 1 to 8 carbon atoms, alkenyl having 2 to 8 carbon
atoms, phenyl, alkoxy having 1 to 8 carbon atoms, and the hydroxyl
group; R is a group selected from the group consisting of alkyl
having 1 to 8 carbon atoms, alkenyl having 2 to 8 carbon atoms, and
phenyl; at least 3 wt % of the R.sup.a and R in the molecule are
alkenyl having 2 to 8 carbon atoms; at least 50% of the total
number of R.sup.a and R in the molecule is alkyl having 1 to 8
carbon atoms; and m=15 to 995. [0032] {7} The silicone release
coating composition according to {5}, characterized in that
component (A) is an organopolysiloxane having a branched structure
and represented by the average siloxane unit formula (3):
[0032]
[(R.sup.bR.sup.c.sub.2SiO.sub.1/2).sub.n(R.sup.dR.sup.c.sub.2SiO.-
sub.1/2).sub.1-n].sub.4(R.sup.c.sub.2SiO.sub.2/2).sub.m1(R.sup.c.sub.2SiO.-
sub.2/2).sub.m2(SiO.sub.4/2) (3)
wherein R.sup.b is alkenyl group having 2 to 8 carbon atoms;
R.sup.c is alkyl group having 1 to 8 carbon atoms or phenyl;
R.sup.d is a group selected from the group consisting of alkyl
having 1 to 8 carbon atoms, alkoxy having 1 to 8 carbon atoms, and
the hydroxyl group; there are at least three R.sup.b in the
molecule; at least 50% of the total number of R.sup.b, R.sup.c, and
R.sup.d in the molecule is alkyl having 1 to 8 carbon atoms; n is 0
or 1; m1 is a number with a value of at least 1; m2 is a number
with a value of at least 0; and m1+m2=15 to 995. [0033] {8} The
silicone release coating composition according to {1},
characterized in that the component (E) comprises at least one
nonionic surfactant selected from the group consisting of polyether
compounds, polyether-modified silicones, water-soluble polyester
compounds, water-soluble polyvinyl alcohols and water-soluble
polyvinylacetates. [0034] {9} The silicone release coating
composition according to any of {1} to {8}, characterized in the
component (G) is a hydrosilylation reaction inhibitor at 0.05-2
weight parts and is noncuring at ambient temperature and cures
under the application of heat. [0035] {10} A low release force
emulsion silicone release coating for films and papers yielded by
curing the silicone release coating composition according to any of
{1} to {9}. [0036] {11} A production method of a low release force
emulsion silicone release coating for films and papers by applying
the silicone release coating composition according to any of {1} to
{9} on at least one side of films and papers and cured at a
temperature of at least 100.degree. C.
[0037] Through the combination between (A) said reactive
organopolysiloxane fluid having specific viscosity (50 to
10,000mPas) and alkenyl content of 0.1 to 3.0 wt %, (B)
diorganopolysiloxane having a viscosity at 25.degree. C. of 5,000
to 150,000 mPas, 0.05 to 0.80 wt. % of alkenyl groups and (C)
organohydrogenpolysiloxane that has a viscosity at 25.degree. C. of
1 to 1,000 mPas and that has at least two silicon-bonded hydrogen
atoms in each molecule, the obtained release coating composition
can provide a lower release force to sticky adhesive, and the
viscosity of the mixture maintains a reasonable base viscosity
suitable for emulsification, and perform lower release force at
same CW: [0038] i) high-speed cure, [0039] ii) cured layer with low
migration, [0040] iii) slippery & good smooth touch of the
coating surface, and iv) good anchorage to the substrate.
[0041] This results in the application use of:
[0042] i) the noise reduction in application stage, and
[0043] ii) protection of operators from friction burn during
repeatedly peeling release liner
BEST MODE FOR CARRYING OUT THE INVENTION
[0044] The silicone release coating composition of the present
invention characteristically comprises [0045] (A) 100 weight parts
of an organopolysiloxane fluid having a viscosity at 25.degree. C.
of 50 to 10,000 mPas and alkenyl content of 0.10 to 3.0 wt %;
[0046] (B) 0.5-40 weight parts of a diorganopolysiloxane
represented by the average structural formula (1), having a
viscosity at 25.degree. C. of 5,000 to 150,000 mPas and alkenyl
content of 0.05 to 0.80 wt %:
[0046]
R.sup.c.sub.3SiO(R.sup.bR.sup.cSIO.sub.2/2).sub.n1(R.sup.c.sub.2S-
iO.sub.2/2).sub.n2SiR.sup.c.sub.3 (1)
wherein R.sup.b is alkenyl having 2 to 8 carbon atoms; R.sup.c is
alkyl group having 1 to 8 carbon atoms or phenyl; n1 is a number
that provides alkenyl content of 0.05 to 0.80 wt %; n2 is a number
with a value of at least 1; and n1+n2 is a number that provides
this component with a viscosity at 25.degree. C. of 5,000 to
150,000 mPas; [0047] (C) 1.5-10 weight parts of an
organohydrogenpolysiloxane that has a viscosity at 25.degree. C. of
1 to 1,000 mPas and that has at least two silicon-bonded hydrogen
atoms in each molecule, wherein the silicon-bonded organic groups
are alkyl group having 1 to 8 carbon atoms or phenyl group, in an
amount sufficient to provide a value of 0.8: 1 to 5: 1 for the
molar ratio of silicon-bonded hydrogen atoms in this
organohydrogenpolysiloxane to the alkenyl groups in components (A)
and (B); [0048] (D) a hydrosilylation reaction catalyst in a
catalytic amount; [0049] (E) surfactant; [0050] (F) water; and
[0051] (G) inhibitor.
[0052] Component (A) is 100 weight parts of at least one
organopolysiloxane fluid selected from the group consists of:
linear organopolysliloxane, branched organopolysiloxane, mixture of
organopolysiloxanes having different alkenyl contents of 0.10 to
3.0 wt. %, and mixture of linear organopolysliloxane and branched
organopolysiloxane.
[0053] Component (A) is a mixture of (A-1) polydimethylsiloxane
having alkenyl groups only in its molecular terminals and (A-2)
polydimethylsiloxane having alkenyl groups in its molecular
terminals and its side-chain positions.
[0054] Component (A) comprises at least one organopolysiloxane
fluid having a branched structure and a viscosity at 25.degree. C.
of 50 to 10,000 mPas, comprising the siloxane units (i) to (iii)
described below, and having a straight-chain moiety comprising a
plurality of siloxane unit (ii)'s, and a branch point comprising
siloxane unit (i), wherein the terminals of the straight-chain
moiety are end blocked by the siloxane unit (iii) [0055] (i) the
siloxane unit represented by the general formula SiO.sub.4/2: 1 or
more [0056] (ii) the siloxane unit represented by the general
formula R.sub.2SiO.sub.2/2: 15 to 995 [0057] (iii) the siloxane
unit represented by the general formula R.sup.aR.sub.2SiO.sub.1/2
in the formulae, R.sup.a is a group selected from the group
consisting of alkyl having 1 to 8 carbon atoms, alkenyl having 2 to
8 carbon atoms, phenyl, alkoxy having 1 to 8 carbon atoms, and the
hydroxyl group, and R is a group selected from the group consisting
of alkyl having 1 to 8 carbon atoms, alkenyl having 2 to 8 carbon
atoms, and phenyl, wherein at least 0.10 to 3.0 wt % of the R.sup.a
and R in the molecule are alkenyl group having 2 to 8 carbon atoms
and at least 50% of the total number of R.sup.a and R in the
molecule is alkyl group having 1 to 8 carbon atoms.
[0058] Component (A) comprises at least one organopolysiloxane
fluid having a branched structure and represented by the average
siloxane unit formula (2):
(R.sup.aR.sub.2SiO.sub.1/2).sub.4(R.sub.2SiO.sub.2/2).sub.m(SiO.sub.4/2)
(2)
wherein R.sup.a is a group selected from the group consisting of
alkyl having 1 to 8 carbon atoms, alkenyl having 2 to 8 carbon
atoms, phenyl, alkoxy having 1 to 8 carbon atoms, and the hydroxyl
group; R is a group selected from the group consisting of alkyl
having 1 to 8 carbon atoms, alkenyl having 2 to 8 carbon atoms, and
phenyl; at least 3 wt % of the R.sup.a and R in the molecule are
alkenyl having 2 to 8 carbon atoms; at least 50% of the total
number of R.sup.a and R in the molecule is alkyl having 1 to 8
carbon atoms; and m=15 to 995.
[0059] Component (A) is an organopolysiloxane having a branched
structure and represented by the average siloxane unit formula
(3):
[(R.sup.bR.sup.c.sub.2SIO.sub.1/2).sub.n(R.sup.dR.sup.c.sub.2SIO.sub.1/2-
).sub.1-n(.sub.4(R.sup.bR.sup.cSIO.sub.2/2).sub.m1(R.sup.c.sub.2SIO.sub.2/-
2).sub.m2(SIO.sub.4/2) (.sup.3)
wherein R.sup.b is alkenyl group having 2 to 8 carbon atoms;
R.sup.c is alkyl group having 1 to 8 carbon atoms or phenyl;
R.sup.d is a group selected from the group consisting of alkyl
having 1 to 8 carbon atoms, alkoxy having 1 to 8 carbon atoms, and
the hydroxyl group; there are at least three R.sup.b in the
molecule; at least 50% of the total number of R.sup.b, R.sup.c, and
R.sup.d in the molecule is alkyl having 1 to 8 carbon atoms; n is 0
or 1; m1 is a number with a value of at least 1; m2 is a number
with a value of at least 0; and m1+m2=15 to 995.
[0060] In preferable component (A), R.sup.b is vinyl or hexyenyl
group, m1 ranges 0 to 20 and total number of siloxane units
(=m1+m2+4) ranges from 50 to 400. The preferred viscosity of
component (A) ranges from 50 to 1,000 mPas. The vinyl content is
within the range of 0.10 to 3.0 wt %.
[0061] Typical examples of this alkyl having 1 to 8 carbon atoms
are methyl, ethyl, propyl, and so forth, with methyl being
preferable. Typical examples of the alkenyl having 2 to 8 carbon
atoms are vinyl, allyl, hexenyl, and so forth, with vinyl being
preferable. The alkoxy having 1 to 8 carbon atoms can be methoxy,
ethoxy, and so forth.
[0062] The R.sup.aR.sub.2SiO.sub.1/2 unit can be exemplified by the
Vi(Me.sub.2)SiO.sub.1/2 unit, He(Me).sub.2SiO.sub.1/2 unit,
(Me).sub.3SiO.sub.1/2 unit, ViMePhSiO.sub.1/2 unit, and
(HO)(Me).sub.2SiO.sub.1/2 unit (wherein Vi denotes the vinyl group,
He denotes the hexenyl group, Me denotes the methyl group, and Ph
denotes the phenyl group; this also applies hereinafter). The
combination of these units (for example, Vi(Me.sub.2)SiO.sub.1/2
unit and (Me).sub.3SiO.sub.1/2 unit) is possible in the same
molecule.
[0063] The R.sub.2SiO.sub.2/2 unit can be exemplified by the
(Me).sub.2SiO.sub.2/2 unit, ViMeSiO.sub.2/2 unit, and
MePhSiO.sub.2/2 unit. The combination of these units (for example,
(Me).sub.2SiO.sub.2/2 unit and ViMeSiO.sub.2/2 unit) is possible in
the same molecule.
[0064] In order to realize an excellent anchorage to the substrate,
the R.sup.aR.sub.2SiO.sub.1/2 unit preferably contains alkenyl
having 2 to 8 carbon atoms, such as the Vi(Me).sub.2SiO.sub.1/2
unit, He(Me).sub.2SiO.sub.1/2 unit, and ViMePhSiO.sub.1/2 unit.
[0065] The silicon-bonded alkenyl groups in component (A) undergo
crosslinking by a hydrosilylation reaction with the silicon-bonded
hydrogen atoms in component (C). At least 2 alkenyl groups must
therefore be present in each molecule; at least 3 alkenyl groups
must be present in each molecule in order to develop excellent
adherence to the sheet-form substrate.
[0066] Component (A) is the base component of the silicone release
coating composition according to the present invention. Preferably,
component (A) may have a low degree of polymerization. The
component (B) preferably has a straight chain structure and has a
high viscosity and hence a high degree of polymerization. The
component (B) possesses pendant vinyl functional group, which can
form covalent bond with cured system by hydrosilylation. And the
trimethylsiloxy terminal is not cured with the system, which can
help lead partial of molecular chain migrate to the surface of
cured release coating. This property can provide the cured release
coating with a slippery touch feeling and low release force.
Siloxane having a moderate viscosity (5,000 to 150,000 mPas at
25.degree. C.) can provide the final release coating bath with
feasible viscosity for multiple rolls coater, and also can have an
appropriate reactivity when vulcanization. Due to this, the
incorporation of just small amounts of component (B) can provide
the cured coating with better slipperiness.
[0067] In this invention, component (A) is not limited as
Q-branched polymer, but includes "linear organopolysiloxane,
Q-branched organopolysiloxanes, mixtures of different linear
organopolysiloxanes, and mixtures of linear- and Q-branched
organopolysiloxanes". Most preferred component (A) is Q-branched
one and mixture thereof.
[0068] Component (B), a diorganopolysiloxane represented by the
average structural formula (1), having a viscosity at 25.degree. C.
of 5,000 to 150,000 mPas and alkenyl content of 0.05 to 0.80 wt %,
preferably 0.05 to 0.50 wt %:
R.sup.c.sub.3SiO(R.sup.bR.sup.cSiO.sub.2/2).sub.n1(R.sup.c.sub.2SiO.sub.-
2/2).sub.n2SiR.sup.c.sub.3 (1)
(wherein R.sup.b is alkenyl having 2 to 8 carbon atoms; R.sup.c is
alkyl group having 1 to 8 carbon atoms or phenyl; each R.sup.b may
be the same or different, and each R.sup.c may be the same or
different in the same molecule, n1 is a number that provides
alkenyl content of 0.05 to 0.80 wt %; n2 is a number with a value
of at least 1; and n1+n2 is a number that provides this component
with a viscosity at 25.degree. C. of 5,000 to 150,000 mPas),
functions to improve the releaseability of the cured coating with
respect to tacky substances and also functions to provide the cured
coating with slipperiness. Component (B) gradually ascends onto the
coating formed when curing occurs through the hydrosilylation
reaction between components (A) and (C) and thereby imparts an
excellent slipperiness to the surface of the cured coating. The
component (B) possesses pendant vinyl functional group (alkenyl
group), which can form covalent bond with cured system by
hydrosilylation. And the trialkylsiloxy terminal is not cured with
the system, which can help lead partial of molecular chain migrate
to the surface of cured release coating. This property can provide
the cured release coating with a slippery touch feeling and low
release force. Siloxane having a moderate viscosity (5,000 to
150,000 mPas at 25.degree. C.) can provide applicable viscosity of
the final release coating bath for multiple rolls coater
processing, and also can have an appropriate reactivity when
vulcanization. In addition, the concept of current invention is
different from said "breed-out" effect, because the pendant alkenyl
group in the siloxane can act as "anchor" point to bond component
(B) into cured system. And siloxane having a viscosity of 5,000 to
150,000 mPas at 25.degree. C. has entanglement effect with cured
system, which would also reduce silicone migration.
[0069] Here, typical examples of the alkyl having 1 to 8 carbon
atoms are methyl, ethyl, propyl, and so forth, with methyl being
preferable. Typical examples of the alkenyl having 2 to 8 carbon
atoms are vinyl, allyl, and hexenyl, with vinyl being preferable.
[0070] The R.sup.bR.sup.cSiO.sub.2/2 unit can be exemplified by the
ViMeSiO.sub.2/2 unit. [0071] The R.sup.c.sub.2SiO.sub.2/2 unit can
be exemplified by the (Me).sub.2SiO.sub.2/2 unit and
MePhSiO.sub.2/2 unit. [0072] The combination of these units is
possible in the same molecule.
[0073] Component (B) includes a component that has silicon-bonded
alkenyl groups in the molecule and thus is capable of undergoing a
hydrosilylation reaction with component (C). Viewed from the
perspective of the residual adhesiveness associated with the cured
coating, there is a preference for component (B) having alkenyl
groups in the molecule and thus being capable of undergoing a
hydrosilylation reaction with component (C)
[0074] With regard to a component (B) that has silicon-bonded
alkenyl groups in the molecule and thus that is capable of
undergoing a hydrosilylation reaction with component (C), an
excessively high alkenyl content results in impaired release
properties and a reduced slipperiness for the cured coating. If
component (B) with too low alkenyl content will cause no-bonding
and more migration, and this content is therefore 0.05 to 0.80 wt %
of the silicon-bonded organic groups in the molecule. The
silicon-bonded alkenyl is present in side-chain position.
[0075] Component (B) has a viscosity at 25.degree. C. of 5,000 to
150,000 mPas, while viewed from the standpoint of the residual
adhesiveness its viscosity is preferably 20,000 to 130,000mPas.
[0076] Component (B) is incorporated at 0.5 to 40 weight parts, in
each case per 100 weight parts of the aforementioned component (A).
The surface of the cured coating has an inadequate slipperiness
when component (B) is incorporated at less than the aforementioned
lower limit. When the aforementioned upper limit is exceeded, the
organopolysiloxane composition assumes an excessively high
viscosity, causing disturbances in the coating of a thin film on
the sheet-form substrate.
[0077] Preferable component (B) has 0.06 to 0.19% of vinyl and/or
hexyenyl groups, and viscosity of 20,000 to 130,000 mPas.
[0078] Component (C), an organohydrogenpolysiloxane that has a
viscosity at 25.degree. C. of 1 to 1,000 mPas and that has at least
2 silicon-bonded hydrogen atoms in each molecule and that has alkyl
having 1 to 8 carbon atoms or phenyl for its silicon-bonded organic
groups, functions as a crosslinking agent for component (A).
Crosslinking occurs through a hydrosilylation reaction between the
silicon-bonded hydrogen atoms in this component and the
silicon-bonded alkenyl groups in component (A). As for component
(B) which contains silicon-bonded alkenyl, the silicon-bonded
alkenyl groups in component (B) also participate in the
hydrosilylation reaction. As a consequence, at least 2
silicon-bonded hydrogen atoms must be present in each molecule and
preferably at least 3 silicon-bonded hydrogen atoms are present in
each molecule.
[0079] The bonding position of the silicon-bonded hydrogen atoms is
not particularly limited, and, for example, they may be bonded in
molecular chain terminal position, side-chain position, or at both
positions.
[0080] The silicon-bonded hydrogen atom content is preferably 0.1
to 20 weight % and more preferably is 0.5 to 18 weight %.
[0081] The silicon-bonded organic groups encompass phenyl and alkyl
having 1 to 8 carbon atoms, such as methyl, ethyl, propyl, butyl,
octyl, and so forth, and preferably at least 50% of the total
number of these organic groups is alkyl having 1 to 8 carbon atoms.
The methyl group is preferred among these alkyl groups from the
standpoint of the properties of the cured coating and the ease of
production. The molecular structure of component (C) is exemplified
by straight chain, branched chain, branched, and cyclic.
[0082] Component (C) has a viscosity at 25.degree. C. of 1 to 1,000
mPas and preferably 5 to 500 mPas. The basis for this is as
follows: when the viscosity at 25.degree. C. is less than 1 mPas,
component (C) readily volatilizes out of the organopolysiloxane
composition; the organopolysiloxane composition takes on long cure
times at above 1,000 mPas.
[0083] This component (C) can be exemplified by
trimethylsiloxy-endblocked methylhydrogenpolysiloxanes,
trimethylsiloxy-endblocked
dimethylsiloxane.cndot.methylhydrogensiloxane copolymers,
dimethylhydrogensiloxy-endblocked
dimethylsiloxane.cndot.methylhydrogensiloxane copolymers, cyclic
methylhydrogenpolysiloxanes, cyclic
methylhydrogensiloxane.cndot.dimethylsiloxane copolymers,
tris(dimethylhydrogensiloxy)methylsilane, and
tetra(dimethylhydrogensiloxy)silane.
[0084] Plural components (C) which are different each other may
also be used together for preparing the same composition.
[0085] Component (C) is incorporated in an amount sufficient to
provide a value of 0.8:1 to 5:1 for the molar ratio of
silicon-bonded hydrogen atoms in component (C) to alkenyl groups in
components (A) and (B) and preferably in an amount sufficient to
provide a value of 0.9:1 to 3:1 for this molar ratio, i.e.
incorporated at 1.5 to 10 weight parts, in each case per 100 weight
parts of the aforementioned component (A)
[0086] The curability is reduced when this molar ratio is less than
the lower limited cited above, while a large peel resistance value
occurs when the cited upper limit is exceeded and practical
releasability is not obtained.
[0087] Component (D) is a catalyst that promotes the
hydrosilylation reaction between the silicon-bonded hydrogen atoms
in component (C) and the silicon-bonded alkenyl groups in component
(A) and functions to bring about crosslinking by an addition
reaction between components (A) and (C). When component (B)
contains one or more silicon-bonded alkenyl groups in each
molecule, this catalyst also promotes the hydrosilylation reaction
with the silicon-bonded alkenyl groups in component (B).
[0088] There are no particular limitations on this component (D)
other than that it is a catalyst used for the hydrosilylation
reaction, and component (D) can be specifically exemplified by
platinum-type catalysts such as chloroplatinic acid,
alcohol-modified chloroplatinic acid, chloroplatinic acid/olefin
complexes, chloroplatinic acid/ketone complexes,
platinum/alkenylsiloxane complexes, platinum tetrachloride,
platinum micropowder, solid platinum supported on a support such as
alumina powder or silica powder, platinum black, olefin complexes
of platinum, carbonyl complexes of platinum, and the powdery
thermoplastic resin (e.g., methyl methacrylate resin, polycarbonate
resin, polystyrene resin, silicone resin, and so forth) that
incorporates a platinum-type catalyst as previously listed.
[0089] Other examples are rhodium catalysts such as
[Rh(O.sub.2CCH.sub.3).sub.2].sub.2, Rh(O.sub.2CCH.sub.3).sub.3,
Rh.sub.2(C.sub.8H..sub.5O.sub.2).sub.4,
Rh(C.sub.5H.sub.7O.sub.2).sub.3,
Rh(C.sub.5H.sub.7O.sub.2)(CO).sub.2,
Rh(CO)[Ph.sub.3P](C.sub.5H.sub.7O.sub.2),
RhX.sub.3[(R.sub.6).sub.2S].sub.3, (R.sub.73P).sub.2Rh(CO).sub.x,
(R.sub.73P).sub.2Rh(CO)H, Rh.sub.2X.sub.2Y.sub.4,
H.sub.aRh.sub.b(E).sub.cCl.sub.d, and
Rh[O(CO)R.sub.3].sub.3-n(OH).sub.n (in the formulas, X is the
hydrogen atom, chlorine atom, bromine atom, or iodine atom; Y is
alkyl, CO, or C.sub.8H.sub.14; R.sub.6 is alkyl, cycloalkyl, or
aryl; R.sub.7 is alkyl, aryl, alkyloxy, or aryloxy; E is an olefin;
a is 0 or 1; b is 1 or 2; c is an integer from 1 to 4; d is 2, 3,
or 4; and n is 0 or 1) and iridium catalysts such as
Ir(OOCCH.sub.3).sub.3, Ir(C.sub.5H.sub.7O.sub.2).sub.3,
[Ir(Z)(E).sub.2].sub.2, and [Ir(Z)(Dien)].sub.2 (in the formulas, Z
is the chlorine atom, bromine atom, iodine atom, or an alkoxy
group; E is an olefin; and Dien is cyclooctadiene).
[0090] Viewed from the perspective of the ability to accelerate the
reaction, chloroplatinic acid, platinum/vinylsiloxane complexes,
and olefin complexes of platinum are preferred, and the
chloroplatinic acid/divinyltetramethyldisiloxane complex,
chloroplatinic acid/tetramethyltetravinylcyclotetrasiloxane
complex, and platinum/alkenylsiloxane complexes, e.g., the
platinum.divinyltetramethyldisiloxane complex,
platinum/tetramethyltetravinylcyclotetrasiloxane complex, and so
forth, are particularly preferred.
[0091] Component (D) is incorporated in a catalytic amount, and in
general is incorporated at 10 to 600 ppm and preferably is
incorporated at 5 to 500 ppm, in each case as the amount of metal
in component (D) with reference to the total weight of the silicone
release coating composition of the present invention.
[0092] Component (E), surfactant, is an ingredient of emulsifying
said components (A)-(B) into water (F), which is not particularly
limited, as long as it can emulsify said components (A)-(B) into
water (F), preferably comprising at least one nonionic surfactant
selected from the group consisting of polyether compounds,
polyether-modified silicones, water-soluble polyester compounds,
water-soluble polyvinyl alcohols and water-soluble
polyvinylacetates.
[0093] Preferred examples of surfactants include the following:
[0094] PVA: polyvinyl alcohol; [0095] Nonionic surfactant 1:
iso-C13 oxo alcohol ethoxylates EO(12) [Lutensol TO12]; [0096]
Nonionic surfactant 2: Polyoxyethylene(23) Lauryl Ether [Brij35 ];
[0097] Nonionic surfactant 3: Polyoxyethylene(4) Lauryl Ether
[Brij30 ].
[0098] In the nonionic surfactant of the present invention, which
is used as ingredient, HLB should be 10-15, the pH should be 6.5 or
less, and the ionic conductance should be 30 .mu.S/cm or less. This
ingredient is used to emulsify a mixture consisting of the silicone
compound.
[0099] Examples of a nonionic surfactant used by the present
invention are an alkyl ether, such as polyoxyethylene lauryl ether
and polyoxyethylene tridecyl ether; an alkyl ester, such as
polyoxyethylene oleate and polyoxyethylene laurate; and an alkyl
aryl ether, such as polyoxyethylene nonylphenyl ether and
polyoxyethylene octylphenyl ether, but from the viewpoint of
emulsification and safety, a polyoxyethylene alkyl ether is
preferred.
[0100] In the present invention, if a surfactant other than one for
which the HLB is 10-15, the pH is 6.5 or less, and the ionic
conductance is 30 .mu.S/cm or less is used, the prepared emulsion
composition deteriorates with time. A cationic and an anionic
surfactant can also be used together in amounts which do not impair
the effect of the emulsion composition of the present invention. By
suitably using a cationic and an anionic surfactant, it is possible
to obtain an improvement in the wettability or leveling properties
of the emulsion.
[0101] The polyvinyl alcohol (hereafter, PVA) in the present
invention is preferred to have a saponification degree of 86-98 mol
%, and the viscosity of a 4% aqueous solution at 20.degree. C.
should be 4-100 mPas. This PVA is a preferred ingredient as an
assistant co-surfactant to promote emulsification with the
surfactant, and stabilizes the formed emulsion. That is to say, the
combination of PVA with other surfactants further improves the
temporal stability of the obtained emulsion. If the saponification
degree is less than 85 mol % or more than 99 mol %, the emulsion
stabilizing effect is inadequate. Also, if the viscosity of a 4%
aqueous solution at 20.degree. C. is less than 3 mPas, the emulsion
stabilizing effect is poor, while if it exceeds 100mPas, the
coating properties of the emulsion deteriorate. The polymerization
degree of PVA whereof the viscosity of a 4% aqueous solution at
20.degree. C. is 4-100 mPas, is equivalent to about 500 to 4,000.
Preferably, the surfactant is a water-soluble polyvinylalchol (PVA)
for improving the wetting performance and rub-off resistance
performance on the cured release coating.
[0102] Component (E) is incorporated at 0.5 to 30 weight parts, in
each case per 100 weight parts of the aforementioned component (A).
The component (E) comprises at least one nonionic surfactant
selected from the group consisting of polyether compounds,
polyether-modified silicones, water-soluble polyester compounds,
water-soluble polyvinyl alcohols and water-soluble
polyvinylacetates.
[0103] Component (F), water, is main component of aqueous phase of
our inventive emulsion, and exemplified as tap water, purified
water, mineral water and the like. In addition, in the aqueous
emulsion of the present invention, optional components which are
water-soluble or water-dispersible may be previously blended in the
water phase unless such component impairs the effect of this
invention.
[0104] Component (F) is incorporated at 60 to 2000 weight parts, in
each case per 100 weight parts of the aforementioned component
(A).
[0105] In addition to the components described in the preceding,
the silicone release coating composition of the present invention
also contains a hydrosilylation reaction inhibitor (G) in order to
render it thermosetting while improving the storage stability by
inhibiting gelation and curing at ambient temperature. This
hydrosilylation reaction inhibitor can be exemplified by acetylenic
compounds, ene-yne compounds, organonitrogen compounds,
organophosphorus compounds, and oxime compounds and can be
specifically exemplified by alkynyl alcohols such as
3-methyl-1-butyn-3-ol, 3,5-dimethyl-1-hexyn-3-ol,
3-methyl-1-pentyn-3-ol, phenylbutynol, and so forth; and by
3-methyl-3-penten-1-yne, 3,5-dimethyl-1-hexyn-3-ene, benzotriazole,
1-ethynyl-1-cyclohexanol, and methylvinylcyclosiloxanes. The amount
of incorporation of this hydrosilylation reaction inhibitor is
generally in the range of 0.05 to 2 weight parts and preferably in
the range of 0.01 to 2 weight parts, in each case per 100 weight
parts of component (A), and may be selected as appropriate in view
of the type of hydrosilylation reaction inhibitor, the properties
and amount of incorporation of the hydrosilylation reaction
catalyst, the amount of alkenyl groups in component (A), and the
amount of silicon-bonded hydrogen atoms in component (C).
[0106] Emulsion Preparation:
[0107] The inventive emulsion can be prepared by emulsifying said
components (A)-(D) including optional silicones with surfactants
and/or co-surfactants into water. Preferably, adding water and
emulsification process is stepwise manner including multiple
emulsification and dispersion procedure. Most preferred
emulsification process includes: [0108] (1) Blend base polymer,
vinyl functional additive, crosslinker, suitable amount of
anchorage promoter together with inhibitor; [0109] (2) Add
surfactants water solution, co-surfactants into the blend oil and
mix; [0110] (3) Weight suitable amount of buffer solution to above
mixture and mix with moderate speed and mix for about 30 minutes;
[0111] (4) Use homoginizer to mix with highest speed for several
miniutes; [0112] (5) Take the pre-emulsion to sonolater for cycling
several times under suitable pressure.
[0113] Release Coating Bath Preparation [0114] (1) Add water to
above base emulsion coating in a beaker and mix until homogeneous;
[0115] (2) Add suitable catalyst emulsion into above diluted
emulsion and mix for 10 minutes; and [0116] (3) Coat the bath on
PET (polyethylene glycol terephthalate) substrate by a coater and
then thermal addition cured in oven.
[0117] An emulsifying device is preferably used in order to bring
about uniform emulsion particles (droplets) in the water. This
emulsifying device can be exemplified by homomixers, paddle mixers,
Henschel mixers, homodispersers, colloid mills, propeller stirrers,
homogenizers, continuous inline emulsifying devices, ultrasonic
emulsifying devices, and vacuum kneaders.
[0118] The particle size for the droplet is not limited, but
preferably, the particle size for the droplet is less than lurn.
Small particle size of the emulsion facilitates molecular transfer
of the composition on the treated substrate.
[0119] A cured low release force emulsion silicone release coating
that exhibits better slipperiness and a suitable peel resistance
value with respect to tacky substances can be formed on the surface
of a sheet-form substrate, by uniformly coating the silicone
release coating composition of the present invention as described
above on the surface of any of various sheet-form substrates, e.g.,
glassine paper, cardboard, clay-coated paper, polyolefin-laminated
paper and particularly polyethylene-laminated paper, thermoplastic
resin film (e.g., polyester film, polyethylene film, polypropylene
film, polyamide film), natural fiber fabrics, synthetic fiber
fabrics, metal foils (e.g., aluminum foil), and so forth, and
heating under conditions suitable for causing components (A) and
(C), or components(A), (B) and (C) to undergo crosslinking through
the hydrosilylation reaction.
[0120] Generally 100 to 200.degree. C. is appropriate for the
curing temperature of the silicone release coating composition of
the present invention on the sheet-form substrate, but curing
temperatures above 200.degree. C. can be used when the substrate
possesses a good heat resistance. The method of heating is not
particularly limited and can be exemplified by heating in a hot air
circulation oven, passage through a long oven, or radiant heating
using an infrared lamp or a halogen lamp. Curing can also be
effected by using heating in combination with exposure to
ultraviolet radiation. When component (D) is a
platinum/alkenylsiloxane complex catalyst, even when this catalyst
is incorporated at 50 to 200 ppm as the amount of platinum metal
with reference to the total quantity of the composition, a cured
coating that exhibits an excellent adherence to sheet-form
substrates and excellent release properties with respect to tacky
substances can be readily obtained in a brief period of time, i.e.,
40 to 1 second, at 100 to 150.degree. C.
[0121] The silicone release coating composition of the present
invention is especially preferably applied on at least one side of
sheet-form substrate with multiple rolls coater. With regard to the
tacky substance that can be applied to the release sheet or film
yielded by the application and curing of the silicone release
coating composition of the present invention onto the surface of a
sheet-form substrate, this tacky substance can be, for example, any
of various pressure-sensitive adhesives and various adhesives, and
examples thereof are acrylic resin-type pressure-sensitive
adhesives, rubber-type pressure-sensitive adhesives, and
silicone-type pressure-sensitive adhesives, as well as acrylic
resin-type adhesives, synthetic rubber-type adhesives,
silicone-type adhesives, epoxy resin-type adhesives, and
polyurethane-type adhesives. Other examples are asphalt, sticky
foods such as mochi (i.e. rice cake), glues and pastes, and bird
lime. Preferred application of present invention is multiple rolls
coater with in situ two side coating process.
[0122] The composition of the present invention is useful for the
formation of cured coatings that exhibit better surface
slipperiness and an excellent low release performance versus tacky
substances, and in particular is well suited as a cured release
coating-forming agent for process paper, asphalt packaging paper,
and various plastic films. In addition, sheet-form substrates
bearing a release coating formed by the cure of the composition of
the present invention are well-suited for use in particular for
process paper, wrapping or packaging paper for tacky substances and
sticky substances, pressure-sensitive adhesive tape,
pressure-sensitive labels, and so forth.
EXAMPLES
[0123] Examples and comparative examples are given below in order
to specifically describe the present invention; however, the
present invention is not limited to the examples that follow. In
the examples and comparative examples that follow, parts are weight
parts in all instances and ppm denotes weight-ppm in all instances.
Here, PDMS means polydimethylsiloxane. Silicones 1 to 9 shown in
below Table 1 are available in market from Dow-Corning
Corporation.
TABLE-US-00001 TABLE 1 Raw material selection for base polymer,
shown in the following table: Nomenclature Chemical description
Siloxane 1 Siloxane composed of Q, D, M, M.sup.vi unit, viscosity
is (Dow-Corning) about 450 mPa s, vi % = 0.47% Siloxane 2 High
molecular weight PDMS gum with terminal vinyl (Dow-Corning) only,
vi % = 0.012% Siloxane 3 PDMS with vinyl at pendant position,
36,000 mPa s, (Dow-Corning) vi % = 0.12%. Trimethylsiloxy capped
Siloxane 4 PDMS with terminal vinyl only, 9,000 mPa s,
(Dow-Corning) vi % = 0.104% Siloxane 5 PDMS with vinyl at pendant
position, 14,500 mPa s, (Dow-Corning) vi % = 0.15%.
Trimethylsiloxycapped Siloxane 6 PDMS with vinyl at pendant
position, 111,000 (Dow-Corning) mPa s, vi % = 0.085%.
Trimethylsiloxy capped Siloxane 7 PDMS with vinyl at pendant
position, 51,000 mPa s, (Dow-Corning) vi % = 0.34%. Trimethylsiloxy
capped Siloxane 8 Dimethyl, methylhydrogen siloxane,
Trimethylsiloxy (Dow-Corning) capped Siloxane 9 alkoxy containing
alkenyl/epoxy functional (Dow-Corning) organopolysiloxane anchorage
promoter MB Methyl butynol Note: Q: SiO.sub.4/2, D:
Me.sub.2SiO.sub.2/2, M: Me.sub.3SiO.sub.1/2, vi: vinyl, M.sup.vi:
ViMe.sub.2SiO.sub.1/2.
[0124] Evaluation Processes: [0125] (1) Coat weight (CW): use X-Ray
to detect the coat weight of silicone by Oxford lab-x 3500
instrument manufactured by Oxford Instruments PLC, Oxon, United
Kingdom. Use uncoated PET as blank. Refer to FINAT Test Method No.7
(FINAT Technical Handbook 7th edition, 2005). [0126] (2) Rub off
(RO): test the coat weight of the coated release coating using
Oxford lab-x 3500 instrument. Then use Abrasion Tester (Elcometer
1720) to rub the sample 30 cycles at a speed of 30 cycles/minute.
Finally, test the coat weight again to measure the relative
anchorage performance. The Anchorage rate is recorded as (CW
after)/(CW before)x 100%. [0127] (3) Delayed RO test: place release
coating samples into 70.degree. C. 80% humidity controlled oven for
3 days, then remove from oven and test the RO. [0128] (4) Release
force (RF): the 180 degree peeling test is used to measure release
force from liner with Tesa 7475 standard tape which was laminated
on coated release coating, loaded weight of 20 g/cm.sup.2 on
laminated sample and left under RT (room temperature) or 70.degree.
C. for 20 hours. After 20 hours, remove the load and wait for 30
minutes. Then test the release force by Chemlnstruments AR-1500.
Refer to FINAT Test Method No.10 (FINAT Technical Handbook 7th
edition, 2005). [0129] (5) SAS (Subsequent Adhesive Strength,
indicator of migration): test tape is laminated by Nitto Denko 31 B
tape on coated release coating, load weight of 20 g/cm.sup.2 and
left under 70.degree. C. for 20 h. After 20 h, remove the load and
wait for 30 minutes at room temperature. Then transfer the 31 B
tape on PET substrate and wait for another 1 h. Test the release
force by ChemInstruments AR-1500. In SAS test, laminate 31 B tape
on PTFE substrate and treat the PTFE sample the same way as release
coating sample. The SAS value is recorded as
RF.sub.release/RF.sub.PTFE.times.100%. Refer to FINAT Test Method
No.11 (FINAT Technical Handbook 7th edition, 2005). [0130] (6)
Coefficient of kinetic friction (CoF): CoF is tested on MXD-02
Coefficient of Friction Tester manufacture by Labthink according to
test standard GB 10006. The bottom side of load cell is covered by
fiber felt. Fix cured release coating and let release coated
surface in contact with bottom of load cell. This was followed by
pulling with conditions of load=200 g and pulling speed=100 mm/min
and the force (g) required for pulling was measured. The force (g)
required for pulling/200 g was designated as the CoF of the cured
coating.
[0131] Composition Formulation of Examples:
[0132] The performance behavior of release composition of branched
siloxane 1 and mixtures of branched siloxane 1 with siloxanes 2-4
having vinyl functional additive was systematically compared in
current invention, shown in the following Table 2:
TABLE-US-00002 TABLE 2 Ex. Siloxane 1 Siloxane 2 Siloxane 3
Siloxane 4 Siloxane 8 Siloxane 9 MB Pt catalyst 1 100 4.28 1 0.125
125 ppm 2 98 2 4.28 1 0.125 125 ppm 3 96 4 4.28 1 0.125 125 ppm 4
95 5 4.28 1 0.125 125 ppm
[0133] The performance behavior of release composition of branched
siloxane 1 and mixtures of branched siloxane 1 with siloxanes 3 and
5-7 having different MW (molecular weight) vinyl pendant functional
additive was compared in current invention, shown in the following
Table 3:
TABLE-US-00003 TABLE 3 Pt Ex. Siloxane 1 Siloxane 3 Siloxane 5
Siloxane 6 Siloxane 7 Siloxane 8 Siloxane 9 MB catalyst 5 100 4.28
1 0.125 125 ppm 6 96 4 4.28 1 0.125 125 ppm 7 96 4 4.28 1 0.125 125
ppm 8 96 4 4.28 1 0.125 125 ppm 9 96 4 4.28 1 0.125 125 ppm
[0134] The performance behavior of release composition of branched
siloxane 1 and mixtures of branched siloxane 1 with different level
of silicone 3 was systematically compared in current invention,
shown in the following Table 4:
TABLE-US-00004 TABLE 4 Ex. Siloxane 1 Siloxane 3 Siloxane 8
Siloxane 9 MB Pt catalyst 10 100 4.28 1 0.125 125 ppm 11 96 4 4.28
1 0.125 125 ppm 12 94 6 4.25 1 0.125 125 ppm 13 90 10 4.14 1 0.125
125 ppm 14 85 15 4.03 1 0.125 125 ppm 15 80 20 3.90 1 0.125 125
ppm
Example 1 (Comparative)
[0135] Procedure:
[0136] Emulsion Preparation: [0137] (i) Blending 100 parts of
Siloxane 1, 4.28 parts of Siloxane 8, 1 part of Siloxane 9, and
0.125 parts of MB; [0138] (ii) Adding 35 parts 10% PVA water
solution and 0.45 parts of Lutensol TO12 from BASF into the blend
oil, and mixing; [0139] (iii) Weighting 110 parts of citric
acid-sodium hydroxide buffer solution with pH value at 5 to above
mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0140] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0141] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0142] Release Coating Bath Preparation: [0143] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0144] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0145] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 2 (Practical)
[0146] Procedure:
[0147] Emulsion Preparation: [0148] (i) Blending 98 parts of
Siloxane 1, 2 parts of Siloxane 2, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0149] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0150] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0151] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0152] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0153] Release Coating Bath Preparation: [0154] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0155] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0156] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 3 (Practical)
[0157] Procedure:
[0158] Emulsion Preparation: [0159] (i) Blending 96 parts of
Siloxane 1, 4 parts of Siloxane 3, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0160] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0161] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0162] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0163] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0164] Release Coating Bath Preparation: [0165] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0166] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0167] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 4 (Practical)
[0168] Procedure:
[0169] Emulsion Preparation: [0170] (i) Blending 98 parts of
Siloxane 1, 5 parts of Siloxane 4, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0171] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol 1012 from BASF
into the blend oil, and mixing; [0172] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0173] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0174] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0175] Release Coating Bath Preparation: [0176] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0177] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0178] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 5 (Comparative)
[0179] Procedure:
[0180] Emulsion Preparation: [0181] (i) Blending 100 parts of
Siloxane 1, 4.28 parts of Siloxane 8, 1 part of Siloxane 9, and
0.125 parts of MB; [0182] (ii) Adding 35 parts 10% PVA water
solution and 0.45 parts of Lutensol TO12 from BASF into the blend
oil, and mixing; [0183] (iii) Weighting 110 parts of citric
acid-sodium hydroxide buffer solution with pH value at 5 to above
mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0184] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0185] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0186] Release Coating Bath Preparation: [0187] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0188] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0189] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 6 (Practical)
[0190] Procedure:
[0191] Emulsion Preparation: [0192] (i) Blending 96 parts of
Siloxane 1, 4 parts of Siloxane 3, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0193] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0194] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0195] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0196] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0197] Release Coating Bath Preparation: [0198] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0199] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0200] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 7 (Practical)
[0201] Procedure:
[0202] Emulsion Preparation: [0203] (i) Blending 96 parts of
Siloxane 1, 4 parts of Siloxane 5, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0204] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0205] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0206] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0207] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0208] Release Coating Bath Preparation: [0209] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0210] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0211] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 8 (Practical)
[0212] Procedure:
[0213] Emulsion Preparation: [0214] (i) Blending 96 parts of
Siloxane 1, 4 parts of Siloxane 6, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0215] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0216] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0217] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0218] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0219] Release Coating Bath Preparation: [0220] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0221] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0222] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 9 (Practical)
[0223] Procedure:
[0224] Emulsion Preparation: [0225] (i) Blending 96 parts of
Siloxane 1, 4 parts of Siloxane 7, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0226] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0227] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0228] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0229] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0230] Release Coating Bath Preparation: [0231] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0232] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0233] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 10 (Comparative)
[0234] Procedure:
[0235] Emulsion Preparation: [0236] (i) Blending 100 parts of
Siloxane 1, 4.28 parts of Siloxane 8, 1 part of Siloxane 9, and
0.125 parts of MB; [0237] (ii) Adding 35 parts 10% PVA water
solution and 0.45 parts of Lutensol TO12 from BASF into the blend
oil, and mixing; [0238] (iii) Weighting 110 parts of citric
acid-sodium hydroxide buffer solution with pH value at 5 to above
mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0239] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0240] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0241] Release Coating Bath Preparation: [0242] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0243] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0244] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 11 (Practical)
[0245] Procedure:
[0246] Emulsion Preparation: [0247] (i) Blending 96 parts of
Siloxane 1, 4 parts of Siloxane 3, 4.28 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0248] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0249] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0250] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0251] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0252] Release Coating Bath Preparation: [0253] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0254] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0255] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 12 (Practical)
[0256] Procedure:
[0257] Emulsion Preparation: [0258] (i) Blending 94 parts of
Siloxane 1, 6 parts of Siloxane 3, 4.25 parts of Siloxane 8, 1 part
of Siloxane 9, and 0.125 parts of MB; [0259] (ii) Adding 35 parts
10% PVA water solution and 0.45 parts of Lutensol TO12 from BASF
into the blend oil, and mixing; [0260] (iii) Weighting 110 parts of
citric acid-sodium hydroxide buffer solution with pH value at 5 to
above mixture and mixing with 500 rpm speed and mixing for about 30
minutes; [0261] (iv) Using homoginizer to mix with 6000 rpm speed
for 2 minutes; and [0262] (v) Taking the pre-emulsion to sonolater
for cycling 6 times under 100 bar pressure.
[0263] Release Coating Bath Preparation: [0264] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0265] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0266] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 13 (Practical)
[0267] Procedure:
[0268] Emulsion Preparation: [0269] (i) Blending 90 parts of
Siloxane 1, 10 parts of Siloxane 3, 4.14 parts of Siloxane 8, 1
part of Siloxane 9, and 0.125 parts of MB; [0270] (ii) Adding 35
parts 10% PVA water solution and 0.45 parts of Lutensol 1012 from
BASF into the blend oil, and mixing; [0271] (iii) Weighting 110
parts of citric acid-sodium hydroxide buffer solution with pH value
at 5 to above mixture and mixing with 500 rpm speed and mixing for
about 30 minutes; [0272] (iv) Using homoginizer to mix with 6000
rpm speed for 2 minutes; and [0273] (v) Taking the pre-emulsion to
sonolater for cycling 6 times under 100 bar pressure.
[0274] Release Coating Bath Preparation: [0275] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0276] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0277] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 14 (Practical)
[0278] Procedure:
[0279] Emulsion Preparation: [0280] (i) Blending 85 parts of
Siloxane 1, 15 parts of Siloxane 3, 4.03 parts of Siloxane 8, 1
part of Siloxane 9, and 0.125 parts of MB; [0281] (ii) Adding 35
parts 10% PVA water solution and 0.45 parts of Lutensol TO12 from
BASF into the blend oil, and mixing; [0282] (iii) Weighting 110
parts of citric acid-sodium hydroxide buffer solution with pH value
at 5 to above mixture and mixing with 500 rpm speed and mixing for
about 30 minutes; [0283] (iv) Using homoginizer to mix with 6000
rpm speed for 2 minutes; and [0284] (v) Taking the pre-emulsion to
sonolater for cycling 6 times under 100 bar pressure.
[0285] Release Coating Bath Preparation: [0286] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0287] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0288] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Example 15 (Practical)
[0289] Procedure:
[0290] Emulsion Preparation: [0291] (i) Blending 80 parts of
Siloxane 1, 20 parts of Siloxane 3, 3.90 parts of Siloxane 8, 1
part of Siloxane 9, and 0.125 parts of MB; [0292] (ii) Adding 35
parts 10% PVA water solution and 0.45 parts of Lutensol TO12 from
BASF into the blend oil, and mixing; [0293] (iii) Weighting 110
parts of citric acid-sodium hydroxide buffer solution with pH value
at 5 to above mixture and mixing with 500 rpm speed and mixing for
about 30 minutes; [0294] (iv) Using homoginizer to mix with 6000
rpm speed for 2 minutes; and [0295] (v) Taking the pre-emulsion to
sonolater for cycling 6 times under 100 bar pressure.
[0296] Release Coating Bath Preparation: [0297] (i) Adding 75 parts
of water to 21.25 parts of above base emulsion coating in a beaker
and mixing until homogeneous; [0298] (ii) Adding 3.75 parts of Dow
Corning Syl-off EM 7975 catalyst emulsion into above diluted
emulsion and mixing for 10 minutes; and [0299] (iii) Coating the
bath on PET substrate by a coater and then thermal addition cured
in oven.
Performance of Examples
[0300] Coating Process Conditions 1: [0301] 1. Substrate: 50 um PET
[0302] 2. Mayer Bar: #8 (using standardized Coating Bar); Coat
weight around 0.75 g/m.sup.2 [0303] 3. Coating cure at 160.degree.
C./60 sec
[0304] The following Table shows the result.
TABLE-US-00005 70.degree. C. Ex. RO.sup.a Delayed RO.sup.b RF RF
SAS CoF 1 87% 92% 7.0 11.8 94% 0.347 2 92% 94% 7.1 13.5 93% 0.225 3
90% 92% 6.0 10.4 92% 0.283 4 91% 93% 6.7 12.2 93% 0.301
.sup.aAnchorage of samples under RT without post cure
.sup.bAnchorage of samples aged in 70.degree. C. 80% humidity
controlled oven for 3 days
[0305] Coating Process Conditions 2: [0306] 1. Substrate: 50 um PET
[0307] 2. Mayer Bar: #3 (using standardized Coating Bar); Coat
weight around 0.35 g/m.sup.2 [0308] 3. Coating cure at 140.degree.
C./60 sec
[0309] The following Table shows the result.
TABLE-US-00006 70.degree. C. Ex. RO.sup.a Delayed RO.sup.b RF RF
SAS 1 92% 91% 8.9 13.6 92% 2 97% 92% 8.6 13.8 92% 3 99% 92% 6.6
11.8 93% 4 97% 94% 6.9 12.1 93% .sup.aAnchorage of samples under RT
without post cure .sup.bAnchorage of samples aged in 70.degree. C.
80% humidity controlled oven for 3 days
[0310] Coating Process Conditions 3: [0311] 1. Substrate: 50 um PET
[0312] 2. Mayer Bar: #6 (using standardized Coating Bar); Coat
weight around 0.95 g/m.sup.2 [0313] 3. Coating cure at 160.degree.
C./60 sec
[0314] The following Table shows the result.
TABLE-US-00007 70.degree. C. Ex. RO.sup.a Delayed RO.sup.b RF RF
SAS 5 94% 86% 7.1 14.4 92% 6 91% 85% 5.5 13.6 95% 7 93% 88% 5.3
13.7 92% 8 94% 91% 5.5 13.6 91% 9 95% 91% 5.4 13.1 93%
.sup.aAnchorage of samples under RT without post cure
.sup.bAnchorage of samples aged in 70.degree. C. 80% humidity
controlled oven for 3 days
[0315] Coating Process Conditions 4: [0316] 1. Substrate: 50 um PET
[0317] 2. Mayer Bar: #3 (using standardized Coating Bar); Coat
weight around 0.40 g/m.sup.2 [0318] 3. Coating cure at 140.degree.
C./60 sec
[0319] The following Table shows the result.
TABLE-US-00008 70.degree. C. Ex. RO.sup.a Delayed RO.sup.b RF RF
SAS 5 87% 87% 12.2 19.3 92% 6 93% 84% 7.0 16.5 91% 7 91% 89% 7.3
15.7 93% 8 89% 85% 7.0 16.0 93% 9 92% 86% 6.9 14.7 94%
.sup.aAnchorage of samples under RT without post cure
.sup.bAnchorage of samples aged in 70.degree. C. 80% humidity
controlled oven for 3 days
[0320] Coating Process Conditions 5: [0321] 1. Substrate: 50 um PET
[0322] 2. Mayer Bar: #6 (using standardized Coating Bar); Coat
weight around 0.85 g/m.sup.2 [0323] 3. Coating cure at 160.degree.
C./60 sec
[0324] The following Table shows the result.
TABLE-US-00009 70.degree. C. Ex. RO.sup.a Delayed RO.sup.b RF RF
SAS 10 88% 81% 6.8 12.8 93% 11 92% 82% 5.7 12.4 92% 12 90% 84% 5.8
12.6 91% 13 91% 82% 5.6 12.2 90% 14 87% 88% 5.7 11.9 89% 15 88% 83%
5.6 12.2 89% .sup.aAnchorage of samples under RT without post cure
.sup.bAnchorage of samples aged in 70.degree. C. 80% humidity
controlled oven for 3 days
INDUSTRIAL APPLICABILITY
[0325] The silicone release coating composition according to the
present invention is useful for the formation, on the surface of
sheet-form substrates, of a cured coating that can provide a lower
release force to sticky adhesive, and possessing excellent
properties including high-speed cure, cured layer with low
migration, slippery & good smooth touch of the coating surface,
and good anchorage to the substrate, with lower release force at
same CW. Sheet-form substrates bearing a cured coating from the
aforesaid composition according to the present invention are useful
for process paper, paper for wrapping or packaging tacky
substances, pressure-sensitive tape, pressure-sensitive labels, and
so forth.
* * * * *