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Description  |
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DESCRIPTION
This invention relates to improved rigid urethane foam systems and more
particularly to an improved blowing system comprising fluorocarbon blowing
agents composed of blends of trichlorofluoromethane (CFC-11) with
dichlorotrifluoroethane (CFC-123 or CFC-123a position isomers of
dichlorotrifluoroethane) which impart significant improvement in the
solubility characteristics of rigid urethane foam systems containing
aromatic polyester polyols. The improved solubility characteristics of the
rigid urethane foam systems permit a relative increase in the amount of
low-cost aromatic polyester polyols used in the formulation.
BACKGROUND OF THE INVENTION
Rigid urethane foams are employed in a variety of uses such as insulation
applications, for example: roofing systems, building panels, refrigerators
and freezers insulation are typical uses. These foams are generally
produced from two component chemical systems. Once component, i.e.
"premix" is composed of a rigid urethane polyol, a fluorocarbon blowing
agent, e.g. a stabilized grade of trichlorofluoromethane (CFC-11); an
amine and/or tin catalyst, a surfactant and possibly a fire retardant
additive. The other component of the foamable composition is an isocyanate
such as pure or crude toluene diisocyanate or a polymeric diisocyanate.
In recent years, aromatic polyester polyols derived from polycarbomethoxy
substituted diphenyls, polyphenyls and benzyl esters of the toluate
family, were introduced for use in rigid urethane foam systems as
substitutes for a portion of the conventional rigid urethane foam polyols
used in the system. These reactive hydroxyl-containing materials which
comprise aromatic polyester polyols that may be derived, for example, from
discarded recycle material, e.g. emptied containers such as polyester soda
pop bottles, or from photographic film, impart the following advantageous
characteristics to the resultant rigid urethane foams into which such
polyols are incorporated:
lower formulation costs
improved compressive strength properties
enhanced flame retardancy
increased use-service temperature of low-density foams.
One of the disadvantages which results in the use of these aromatic
polyester polyols in rigid urethane foam systems, however, is a decrease
in the compatibility or solubility of the fluorocarbon blowing agent,
trichlorofluoromethane, CFC-11, in the system. The presence of
fluorocarbon solubility in the system is important for at least the
following reasons:
(a) to insure metering of stoichiometric correct amounts of two component
systems on commercial foam production equipment; and
(b) to increase the amount of fluorocarbon blowing agent in the closed-cell
structure of resultant rigid urethane foams to produce optimum insulation
properties.
While a variety of chlorofluoroalkane blowing agents have been used for
urethane systems in the past, none of the known systems which have been
employed heretofore have been satisfactory for the production of composite
rigid urethane foams that includes therein these aromatic polyester
polyols.
In rigid urethane foam systems, if the fluorocarbon blowing agent is not
completely soluble or miscible in the "premix" component of the system,
the insoluble portion of the fluorocarbon will separate as a specific
layer on the bottom of the "premix" component container during storage.
When the "premix" component container, e.g. 55 gallon drum is put into use
for rigid foam production, processing and foam appearance and physical
property problems could arise because the "premix" component is not
homogeneous. The stoichiometric amount of "premix" component required to
react with a specific unit weight of isocyanate would be disproportional
and the above indicated processing drawback in appearance and physical
property problems could ensue.
Fluorocarbons as a class of insulating gases exhibit the lowest thermal
conductivity values when compared to other gases such as air, nitrogen,
carbon dioxide, water vapor, etc. In rigid urethane foams systems,
fluorocarbons not only act as blowing agents to produce the foam by virtue
of their volatility, but also are encapsulated or entrained in the closed
cell structure of the rigid foam and are the major contributor to the low
thermal conductivity properties of rigid urethane foams used in insulation
applications.
If the required amount of fluorocarbon is not present in the resultant
rigid urethane foam due to insolubility of some of the fluorocarbon in the
"premix" component of the liquid foam system, i.e. nonhomogeneous "premix"
component, then the processing characteristics of the foam system will
change and desired foam appearance and physical properties, e.g. density,
loadbearing, thermal conductivity, etc. wouold not be achieved. Therefore,
it is necessary for the fluorocarbon to be completely soluble or miscible
in the "premix" component of the liquid foam system in order to obtain the
desired results.
Accordingly, a need exists for an improved blowing agent for rigid urethane
systems containing aromatic polyester polyols which have the desired
solubility, compatibility and stability and which does not adversely
affect the resultant rigid foam properties.
SUMMARY OF THE INVENTION
In accordance with the invention, rigid urethane and isocyanurate foams
based on conventional polyethers and aromatic polyester polyols are
prepared using blends of (a) trichlorofluoromethane (CFC-11) and (B)
dichlorotrifluoroethane (CFC-123 or CFC-123a). The desired ratio of
CFC-123 or CFC-123a to CFC-11 is preferably in the range of 1:9 to 3:7,
respectively and the total blowing agent blend is present in amounts of
about 2 to 40 parts by weight based on the total weight of the polyol.
Chemicals systems using this blowing agent blend exhibit improved
solubility characteristics with no significant adverse effect on resultant
rigid foam properties. We have found that this particular fluorocarbon
blowing agent blend imparts significant improvement in the solubility
characteristics of rigid urethane foam systems containing aromatic
polyester polyols. The increased solubility of the CFC-11/CFC-123 or
CFC-11/CFC-123a blowing agent blends over CFC-11 alone in typical rigid
urethane foam premix systems containing variable concentrations of
aromatic polyester polyol, has been found to be substantial. Preparation
of rigid urethane foams using the system of the invention has shown that
improved solubility of CFC-11 blends with CFC-123 or CFC-123a permits an
important increase in the amount of aromatic polyester polyol that can be
used in the formulation without imparting any significant adverse
properties to physical characteristics of foams produced from CFC-11 over
these foams which do not contain the aromatic polyester polyols. The
blowing agent blend of the invention improves the solubility and
compatibility characteristics of CFC-11 expanded insulation foams produced
from premixes that contain aromatic polyester polyols. The foam systems
which contain a significant proportion of aromatic polyester polyol have
recently emerged as substitutes for conventional polyols used in rigid
urethane systems that would not otherwise contain polyester polyols. Those
compositions which contain aromatic polyester polyols impart the following
desirable characteristics to rigid urethane foams: lower formulation
costs, improved compressive strength properties, enhanced flame
retardancy, and increased use-service temperature of low-density foams.
DESCRIPTION OF THE PREFERRED EMBODIMENT
In accordance with the invention, rigid urethane foam systems containing
aromatic polyester polyols may be compounded with fluorocarbon blowing
agent that comprise a blend of (a) CFC-11 and (b) CFC-123 or CFC-123a, to
yield improved compatibility and solubility properties to the foamable
composition. Advantageously, such properties are retained over long term
storage periods. Additionally, an important aspect of the invention
resides in the fact that the particular blowing agent system herein
described permits an increase in the amount of low cost aromatic polyester
polyols that can be introduced into the rigid urethane foam formulations
with no significant effect on fluorocarbon compatibility in the system.
The composition of the fluorocarbon blends may vary from about 80-95% of
CFC-11 and 5-20% of CFC-123 or CFC-123a based on the equivalency of the
amount of CFC-11 normally used in the fomulation. For example,
substitution of a 95/5 blend of CFC-11/CFC-123 for CFC-11 in a rigid
urethane foam system containing 40% of the aromatic polyester polyol as
part of the polyol, resulted in complete fluorocarbon solubility, whereas
the system containing the CFC-11 alone exhibited only 90% fluorocarbon
solubility. No significant differences in resultant rigid urethane foam
reactivity, appearance or physical properties were observed between foam
prepared from CFC-11 and the 95/5 blend of CFC-11/CFC-123.
Similarly, the substitution of a 90/10 blend of CFC-11/CFC-123a for CFC-11
in a rigid foam formulation containing 50% of an aromatic polyester polyol
such as that available commercially as Terate 203 from Hercules, Inc., as
part of the polyol, resulted in complete fluorocarbon solubility where the
same system containing CFC-11 exhibited only 85% fluorocarbon solubility.
Again, no significant differences in reactivity, appearance or physical
properties were observed between foams produced from CFC-11 or the 90/10
blend of CFC-11/CFC-123a.
The use of the specified blends of CFC-11 with CFC-123 or CFC-123a results
in improved fluorocarbon compatibility or solubility in rigid urethane
foam systems containing aromatic polyester polyols, with no significant
effect on resultant rigid urethane foam properties.
The invention is further illustrated by the following specific examples in
which parts or percentages are by weight unless stated otherwise.
EXAMPLE I
CFC-11 solubility was determined in a typical free-rise rigid urethane foam
premix component containing variable concentrations of the aromatic
polyester polyol, Terate 203.
Samples of premix component containing CFC-11 were placed in calibrated
glass vials, stored for one month at 70.degree. F. and fluorocarbon
solubility determined from the amount of fluorocarbon phase separation of
the end of the storage period. Data for this example is set forth in Table
I.
TABLE I
__________________________________________________________________________
GENETRON .RTM. 11SBA SOLUBILITY IN A RIGID URETHANE FOAM PREMIX
CONTAINING AROMATIC POLYESTER POLYOL
Systems A B C D E F G H I J
__________________________________________________________________________
Pluracol.sup.1 879 (415-OH#)
100
90 80 70 60 50 40 30 20 10
Terate.sup.2 203 (315-OH#)
-- 10 20 30 40 50 60 70 80 90
Silicone.sup.3 L-5340
1.5
1.5
1.5
1.5
1.5
1.5
1.5
1.5
1.5
Non
Thancat.sup.4 TD-33
0.5
0.5
0.5
0.5
0.5
0.5
0.5
0.5
0.5
Uni-
Thancat.sup.5 DME
0.2
0.2
0.2
0.2
0.2
0.2
0.2
0.2
0.2
form
Catalyst.sup.6 T-12
0.1
0.1
0.1
0.1
0.1
0.1
0.1
0.1
0.1
--
Genetron.sup.7 11SBA
35
35 35 35 35 35 35 35 35 --
% Genetron 11SBA
Solubility % with increased polyester polyol
100
100
100
100
90.35
84.78
83.49
74.71
55.61
--
(After 4 weeks at 70.degree. F.)
__________________________________________________________________________
.sup.1 Trademark of BASF Wyandotte Corp. rigid foam polyether polyol
.sup.2 Trademark of Hercules Inc. aromatic polyester polyol
.sup.3 Union Carbide Corp. silicone surfactant
.sup.4 Trademark of Texaco, Inc. 33% triethylene diamine in propylene
glycol
.sup.5 Texaco, Inc. N,N--dimethylethanolamine
.sup.6 Metal & Thermit Co. dibutyltin dilaurate
.sup.7 Trademark of Allied Chemical Co. a stabilized grade of
trichlorofluoromethane (CFC11) containing a 0.5% of alpha methyl styrene
From this example, it is seen that CFC-11 solubility in the rigid urethane
foam premix decreased from 100% to 90.4% at a aromatic polyester polyol
concentration of 40% of the polyol composition.
EXAMPLE II
Blends of CFC-11 and CFC-123 were prepared based on the equivalents of
fluorocarbon blowing agent present in the premix in Example 1, i.e.:
______________________________________
Fluorocarbon Equivalent Weight
______________________________________
CFC-11 137.4
CFC-123 153.0
______________________________________
##STR1##
TABLE II
______________________________________
CFC-11/CFC-123 BLENDS
CFC-11 CFC-123 Wt. of Blend
Blend Equivalents/gms
Equivalents/gms
Used in Premix
______________________________________
95/5 0.242/33.25 0.0127/1.95 35.2 gms
90/10 0.2295/31.53 0.0255/3.90 35.4 gms
85/15 0.2168/29.79 0.0382/5.85 35.6 gms
80/20 0.204/28.03 0.051/7.80 35.8 gms
______________________________________
In the premix containing 40% of Terate 203 as part of the polyol in Example
1, 35.2 grams of 95/5 blend of CFC-11/CFC-123 were substituted for 35
grams of CFC-11 and fluorocarbon solubility determined after one month
storage at 70.degree. F. No phase separation was observed at the end of
the one month period. It is seen from this example that the fluorocarbon
solubility increased from 90.4% (CFC-11) to 100% using the 95/5 blend of
CFC-11/CFC-123.
EXAMPLE III
Similar equivalent blends of CFC-11/CFC-123a were prepared as in Example 2.
In the premix containing 50% of aromatic polyester polyol (Terate 203) as
part of the polyol in Example 1, 35.4 grams of 90/10 blend of
CFC-11/CFC-123a were substituted for 35 grams of CFC-11 and fluorocarbon
solubility determined after one month storage at 70.degree. F. The
fluorocarbon solubility increased from 84.8% (CFC-11) to 100% using the
90/10 blend of CFC-11/CFC-123a.
EXAMPLE IV
Bench-scale rigid urethane foams were prepared from the premix in Example I
containing 50% of aromatic polyester polyol as part of the polyol
composition using (a) CFC-11, (b) 90/10 blend of CFC-11/CFC-123 and (c)
90/10 blend of CFC-11/CFC-123a. Resultant foam reactivity, appearance and
physical properties were compared and are set forth in Table III.
No significant differences in reactivity, appearance or physical properties
were observed among bench scale foams prepared with CFC-11, a 90/10 blend
of CFC-11/CFC-123 or a 90/10 blend of CFC-11/CFC-123a.
TABLE III
______________________________________
BENCH SCALE RIGID URETHANE FOAMS
Parts By Weight
(a) (b) (c)
______________________________________
Formulation
Pluracol 879 50 50 50
Terate 203 50 50 50
Silicone L-5340 1.5 1.5 1.5
Thancat TD-33 0.5 0.5 0.5
Thancat DME 0.2 0.2 0.2
Catalyst T-12 0.1 0.1 0.1
Genetron 11 SBA 35 -- --
90/10 G-11 SBA*/CFC-123
-- 35.4 --
90/10 G-11 SBA*/CFC-123a
-- -- 35.4
Lupranate.sup.1 M-20 at 1.29 Index
112.2 112.2 112.2
Reactivity
Cream Time, sec. 10 10 10
Gel Time, sec. 30 30 30
Tack Free Time, sec. 40 40 40
Appearance
Cell Structure Fine Fine Fine
Physical Properties
Density, lbs/cu. ft. 1.75 1.72 1.81
Compression Load at 10%, psi
Parallel to rise 32.4 32.8 32.9
Perpendicular to rise
13.4 13.2 14.3
Physical Properties
Porosity, % closed cells
96 97 98
K-Factor, BTU/(Hr) (Sq. Ft.) (.degree.F./in.)
0.150 0.148 0.135
______________________________________
*Genetron 11SBA
.sup.1 Trademark of BASF Wyandotte Corp. polymethylene
polyphenylisocyanate, functionality 2.7 approx.
EXAMPLE V
Machine-made rigid urethane foams were prepared on a Martin Sweets Co.
Modern Module III urethane foam machine at a delivery rate of
12-lbs/minute using the premix system in Example 1 containing 50% Terate
203 as part of the polyol composition using (a) Genetron 11 SBA; (b) a
90/10 blend of Genetron 11 SBA/CFC-123; and (c) a 90/10 blend of Genetron
11 SBA/CFC-123a, as blowing agent compositions.
No significant differeneces in reactivity, appearance or physical
properties were observed among machine-made foams produced with CFC-11,
90/10 blend of CFC-11/CFC-123, or a 90/10 blend of CFC-11/CFC-123a as
blowing agents.
The data is summarized in Table IV.
TABLE IV
______________________________________
MACHINE MADE RIGID URETHANE FOAMS
Parts By Weight
(a) (b) (c)
______________________________________
Formulation
Pluracol 879 50 50 50
Terate 203 50 50 50
Silicone L-5340 1.5 1.5 1.5
Thancat TD-33 0.5 0.5 0.5
Thancat DME 0.2 0.2 0.2
Catalyst T-12 0.1 0.1 0.1
Genetron 11 SBA 35 -- --
90/10 G-11 SBA/CFC-123
-- 35.4 --
90/10 G-11 SBA/CFC-123a
-- -- 35.4
Lupranate M-20 at 1.29 Index
112.2 112.2 112.2
Reactivity
Cream Time, sec. 15 16 17
Gel Time, sec. 35 36 35
Tack Free Time, sec. 55 59 54
Appearance
Cell Structure Fine Fine Fine
Physical Properties
Density, lbs/cu. ft. 1.70 1.80 1.82
Compression Load at 10%, psi
Parallel to rise 34.8 30.4 28.5
Perpendicular to rise
12.3 12.6 13.8
Porosity, % closed cells
93 94 95
K-Factor, BTU/(Hr) (Sq. Ft.) (.degree.F./in.)
0.151 0.150 0.147
______________________________________
From the foregoing, it is thus seen that a rigid urethane foam chemical
system can be compounded containing aromatic polyester polyols with
fluorocarbon blowing agent blends of CFC-11/CFC-123 or CFC-11/CFC-123a
with improved compatibility or solubility properties over long term
storage periods. Additionally, the amount of low-cost aromatic polyester
polyols which may be introduced into formulations may be increased with no
significant effect on fluorocarbon compatibility in the system.
It will be understood from the foregoing that depending on the period of
time that the polyurethane foam premix components will be stored before
use that the inclusion of a stabilizer in the fluorocarbon component may
be advisable, i.e., a stabilized grade may be employed. Stabilization of
fluorocarbons is disclosed, for example, in U.S. Pat. No. 3,352,789.
Various modifications to the foregoing will be apparent to one skilled in
the art from the disclosure and teaching herein provided such
modifications are not to be construed as limiting the invention except to
the extent that a given limitation is set forth in the claims which follow
.
* * * * *
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Description  |
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