Bakeware release coating

Details Bakeware release coating Bakeware release coating

1999-12-13

2001-06-12

Nakarani, D. S. (Department: 1773)

Stock material or miscellaneous articles

Composite

Of silicon containing

C428S447000, C524S265000, C524S266000, C524S267000, C524S268000, C525S477000, C528S017000, C528S018000, C528S019000, C528S033000

Reexamination Certificate

active

06245431

ABSTRACT:

TECHNICAL FIELD
The present invention is directed to an organosiloxane composition, more specifically, to an organosiloxane release coating useful for coating bakeware.
BACKGROUND
Release coatings have long been used in industrial bakeries to provide release of baked goods. The coatings typically provide non-crazing, release coatings required for the several hundred baking cycles at temperatures as high as 550° F. before requiring recoating of the baking pan. These organosiloxane coatings are typically resinous coatings which contain aryl substituted polyorganosiloxanes such as CH
3
SiO
3/2
, C
6
H
5
SiO
3/2
, C
6
H
5
(CH
3
)SiO
3/2
, and (C
6
H
5
)
2
SiO units (see, for example, U.S. Pat. No. 4,677,147, U.S. Pat. No. 4,681,908, U.S. Pat. No. 4,585,705, and U.S. Pat. No. 4,895,766). There are increasing toxicological concerns over aryl functional organosiloxanes being used for food contact applications such as coating baking pans. Unfortunately, coatings based solely on non-aryl substituted siloxanes have not yielded coatings which provide the performance of aryl substituted polysiloxanes.
What is needed in the art is a non-aryl substituted polysiloxane coating that provides the high performance characteristics of known aryl substituted polysiloxane coatings.
SUMMARY OF THE INVENTION
In a first aspect, the present invention is directed to a curable silicone bakeware release composition comprising: a) a functional silicone resin containing RSiO
3/2
, R
2
SiO, and R
3
SiO
1/2
units, wherein each R is independently alkyl, OH, alkoxy or acyloxy, provided that at least one of R per molecule is OH, alkoxy or acyloxy; b) a functional polydialkylsiloxane fluid; c) a polydialkylsiloxane fluid; and d) an effective amount of a curing agent, wherein the composition is substantially free of aryl substituted silicone compounds. Preferably, each R is independently (C
1
-C
6
)alkyl, (C
1
-C
6
)alkoxy and (C
6
-C
12
)acyloxy, more preferably methyl, such that the resin has from about 0.05 up to about 10 weight percent hydroxy, alkoxy or acyloxy radicals attached to the silicon atoms.
The composition of the present invention is effective in providing a release coating for bakeware.
As used herein, the terms “crazing” means cracking of the coating as observed after being placed in a 550° F. oven for 24 hours, and “non-crazing” means no observable change in the appearance of the coating after being placed in a 550° F. oven for 24 hours.
DETAILED DESCRIPTION OF THE INVENTION
Preferably, the first preferred embodiment of the composition of the present invention comprises, from about 35.0 to about 99.895 parts by weight (“pbw”), more preferably from about 35.0 to about 55.0 pbw, of the functional resin; from about 0.1 to about 2.0 pbw, more preferably from about 0.4 to about 1.6 pbw, of the functional polydimethylsiloxane fluid; from about 0.005 to about 2.0 pbw, more preferably from about 0.01 to about 2.0 pbw, of the polydimethylsiloxane fluid; and from about 0.1 to about 2.0 pbw, more preferably from about 0.2 to about 1.0 pbw, of the curing agent.
A highly preferred embodiment of the present invention further comprises from about 55.0 to about 65.0 pbw, more preferably from about 56.0 to about 64.0 pbw, even more preferably from about 58.0 pbw to about 62.0 pbw of a solvent or mixture of solvents.
As used herein, the term “substantially free of aryl substituted silicone compounds” means less than about 5 parts per billion (“ppb”), preferably less than about 2 ppb, more preferably no detectable level of aryl substituents are present in the cured composition.
The functional resin may be a single silicone resin or a combination of silicone resins. Compounds suitable as the functional resin component of the present invention are those resins or combinations of resins comprised of RSiO
3/2
, R
2
SiO, and R
3
SiO
1/2
units and silanol, alkoxy, acyloxy and the like functional end groups, where each R is independently alkyl, preferably (C
1
-C
6
)alkyl, most preferably methyl. The functional resin is highly branched. Preferably, the functional resin has a viscosity of from about 10 to about 10,000 centistokes and a solids content of from about 40 to about 60 percent at 25° C. Resins suitable for use in the present invention preferably have from about 0.05 up to about 10 percent by weight hydroxy, alkoxy or acyloxy functional end groups.
In a preferred embodiment, the functional resin comprises one or more compounds of the structural formula (I):
M
z
D
x
T
y
  (I)
wherein:
M is R
1
3
SiO
1/2
;
D is R
2
2
SiO
2/2
; and
T is R
3
SiO
3/2
;
each R
1
, R
2
and R
3
is independently alkyl, OH, alkoxy or acyloxy, provided that at least one of R
1
, R
2
and R
3
per molecule is OH, alkoxy or acyloxy; and x, y and z are each integers, wherein 5≦x≦20, 80≦y≦95 and 0≦z≦3, more preferably wherein 5≦x≦15, 80≦y≦90 and 0≦z≦2 or 1≦z≦3. Preferably, R
1
, R
2
and R
3
are (C
1
-C
6
)alkyl, (C
1
-C
6
)alkoxy and (C
6
-C
12
)acyloxy, more preferably methyl, such that the resin has from about 0.05 up to about 10 weight percent hydroxy, alkoxy or acyloxy radicals attached to the silicon atoms.
As used herein, the term “(C
1
-C
6
)alkyl” means a linear or branched alkyl group containing from 1 to 6 carbons per group, such as, for example, methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, hexyl, preferably methyl.
As used herein, the term “(C
1
-C
6
)alkoxy” means a linear or branched alkoxy group containing from 1 to 6 carbons per group, such as, for example, methoxy, ethoxy, propoxy, and butoxy.
Functional resins suitable for use in the present invention include, for example, silanol-stopped dimethylsiloxane, and trimethylsiloxy-stopped dimethylsiloxane.
Suitable functional resins are made by known methods, such as, for example, the hydrolysis and condensation of chlorosilanes or alkoxy silanes, and are commercially available. The functional resin can be used as is or in a solvent, such as, for example, xylene, toluene, naphtha and other similar organic solvents.
Compounds suitable as the functional polydialkylsiloxane fluid component of the present invention are those which are a linear or branched, preferably mostly linear, more preferably, linear, silicone polymer and which contain reactive functional groups. Preferably, the reactive functional groups are silanol, alkoxy, acyloxy and the like such that the fluid has from about 0.05 up to about 10 weight percent hydroxy, alkoxy or acyloxy radicals attached to the silicon atoms. Preferably, the functional polydialkylsiloxane is a polydimethylsiloxane fluid having a viscosity of from about 5 to about 100,000 centipoise at 25° C., more preferably, of from about 100 to about 50,000 centipoise at 25° C., even more preferably, of from about 1000 to about 35,000 centipoise at 25° C.
In a preferred embodiment, the functional polydialkylsiloxane fluid component comprises one or more polysiloxanes having repeating units of the average structural formula (II):
R
4
a
SiO
(4-a)/2
  (II)
wherein:
each R
4
is independently a substituted or unsubstituted hydrocarbon radical having from about 1 to about 10 carbon atoms or OH, alkoxy or acyloxy, preferably OH, (C
1
-C
6
)alkoxy or (C
6
-C
12
)acyloxy, provided that at least one R
4
group per molecule is OH, alkoxy or acyloxy, and on average, 1≦a≦3, preferably, on average, a is 2. Preferably, R
4
is OH.
In a preferred embodiment, the functional polyalkylsiloxane fluid comprises fluid siloxanes having hydroxy or alkoxy endblocking, wherein a small portion of the fluid siloxanes are M units, wherein R
4
is methyl. As used herein, “M unit” refers to R
4
3
SiO
1/2
. Preferably, only a small portion of the fluid siloxanes are T units. As used herein, “T unit” refers to R
4
SiO
3/2
, and R
4
is preferably methyl. An example of a functional polyalkylsiloxane fluid suitable for use in the present invention is silanol-stopped dimethylsiloxane fluid.
In a more preferred embodiment, the functional fluid comprises one or more compounds of the

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