Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – At least one aryl ring which is part of a fused or bridged...
Reexamination Certificate
2000-10-30
2002-01-15
Cain, Edward J. (Department: 1714)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
At least one aryl ring which is part of a fused or bridged...
C524S590000, C524S591000, C524S839000, C524S840000
Reexamination Certificate
active
06339125
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention is directed to a new class of polyurethane dispersions. More specifically, the present invention is directed to a non-corrosive and non-toxic cationic polyurethane dispersion containing hydrophobic polyolefin segments in its backbone and operable in acidic medium.
2. Description of the Prior Art
The utilization of polyurethane dispersions as adhesives, coatings and sizing agents for glass fibers and mineral fillers is well known. Although polyurethane dispersions are utilizable in the aforementioned applications, a major problem associated with that use in the prior art occurs when the substrate on or into which the polyurethane dispersion is disposed, is a polyolefin. The hydrophobic nature of polyolefins makes bonding of polyurethane dispersion sizing agents, coatings and adhesives difficult due to the polar nature of polyurethane dispersions and the non-polarity of polyolefins.
Another problem known to those skilled in the art is the difficulty of utilizing polyurethane dispersions in acidic media. This problem has been addressed in the prior art with indifferent results. That is, although prior art cationic polyurethane dispersions could be used in acidic media their use was discouraged due to their high toxicity and high corrosivity.
Yet a third problem, in reality a corollary of the problem associated with the hydrophobicity of polyurethane dispersions, is the poor adhesivity of polyurethane dispersion sized fibers and fillers in hydrophobic polymeric matrices. This difficulty in the prior art is particularly pronounced in the case of highly hydrophobic polyolefin matrices. As such, this problem has discouraged the utilization of polyurethane dispersion sizing compositions for fiber and filler employed in the reinforcement of hydrophobic polymeric matrices, especially polyolefins. Obviously, reinforcing fillers and fibers must securely adhere to the polyolefin matrix in order for the reinforcing agent to be effective. Therefore, because of the poor adhesion between polyolefins and polyurethane dispersions, polyurethane dispersion sizing composition have not been utilized in this application.
The above problems have been addressed only in part in the prior art. The preparation of cationic polyurethane dispersions is described in U.S. Pat. Nos. 4,160,065 and 5,561,187. U.S. Pat. No. 4,160,065 discloses a latex prepared in an aqueous system by reacting a quaternized NCO-prepolymer with water and a chain extender. The resulting prepolymer is chain extended by reaction with a difunctional or polyfunctional reagent containing primary amino groups. U.S. Pat. No. 5,561,187 describes the preparation and use of quaternized bis(hydroxylalkyl)amines. These amines are produced by reacting a tertiary amine and an alkylene oxide in a strong acid system.
The modification of polyurethane dispersions with hydroxy-terminated polyolefins has been reported, albeit this modification in cationic polyurethane dispersions is unknown. Specifically, U.S. Pat. Nos. 4,507,430 and 5,672,653 describe anionic polyurethane dispersions containing polyolefin polyols. However, as stated above, the preparation of equivalent cationic dispersions is not reported in the prior art. This is believed due to the excessive hydrophobicity of polyalkaldiene polyols which makes dispersibility in water very difficult. In addition, the functionality of polyalkadiene polyols increases viscosity which increases the possibility of prepolymer gellation.
The aforementioned difficulties in the prior art evidence the strong need in the art for a new class of cationic polyurethane dispersions which are compatible with hydrophobic polymer matrices, are easy to handle, non-corrosive and can be employed in acidic media.
BRIEF SUMMARY OF THE INVENTION
A new class of cationic polyurethane dispersions has now been developed which overcomes the prior art problems of polyurethane dispersions which are incompatible with polyolefin matrices. Moreover, since this new class of polyurethane dispersions is cationic, these dispersions can be employed in acidic media without the attendant problems of toxicity or corrosion. The cationic polyurethane dispersions of the present invention are thus characterized by good adhesion to hydrophobic matrices, especially polyolefins, which have presented problems in the prior art.
In accordance with the present invention a cationic polyurethane dispersion is provided. The cationic polyurethane dispersion of the present invention includes a reaction product of a prepolymer and a chain extender. The prepolymer comprises a reaction product of a hydroxylated polymer selected from the group consisting of hydroxylated polyethers, hydroxylated polyesters and mixtures thereof, a hydroxylated polyalkadiene, a polyisocyanate, a bis(hydroxyalkyl) quaternary ammonium group-containing diol and, optionally, an ester of a hydroxylated fatty acid containing about 12 to about 20 carbon atoms.
DETAILED DESCRIPTION
The present invention is directed to cationic polyurethane dispersions which incorporate therein quaternary ammonium groups. The polyurethane dispersion is prepared by dispersing a prepolymer in water and extending it with water or hydrazine. The prepolymer is formed by reacting, at elevated temperature, a quaternary ammonium group-containing diol with a hydroxylated polyalkadiene, a polyisocyanate and one or more optional components. These optional components include a hydroxylated polymer selected from the group consisting of a polyether polyol, a polyester polyol and mixtures thereof, an ester of a fatty acid containing about 12 to about 20 carbon atoms containing hydroxyl groups and a polyepoxide.
The prepolymer reaction occurs at a temperature in the range of between about 70° C. and about 95° C. over a period of between about 2 and about 5 hours. The reaction continues until the free isocyanate content reaches or comes very close to the calculated value, as determined by standard titration with dibutylamine.
The polyurethane dispersion prepolymer-forming reaction is characterized by the polyisocyanate being reacted in a concentration of between about 30% and about 150% in excess of the stoiciometric concentration required to completely react with the hydroxyl groups. Moreover, the quaternary ammonium group-containing diol is present in a concentration sufficient to provide adequate stability to the polyurethane dispersion in water. The thus formed prepolymer is thereupon dispersed in water under vigorous agitation. A polyurethane dispersion is formed by reacting the free isocyanate end-groups with an appropriate chain extender, such as water or hydrazine, to produce a stable aqueous cationic polyurethane dispersion.
A first component of the prepolymer reaction product of the present invention is a hydroxylated polyalkadiene. The hydroxylated polyalkadiene may or may not be hydrogenated. Moreover, if the hydroxylated polyalkadiene is hydrogenated, the degree of hydrogenation may be partial or complete. Although the degree of hydroxylation is limited only by the minimum presence of two hydroxyl groups, it is indeed preferred that the hydroxylated polyalkadiene be a diol.
Of the hydroxylated polyalkadienes within the contemplation of the present invention hydroxylated polybutadiene is preferred. Thus, a particularly preferred hydroxylated polyalkadiene is a diol of polybutadiene.
A second reactant employed in the formation of the polyurethane dispersion prepolymer is a polyisocyanate. Any compound which includes at least two isocyanate groups is within the contemplation of the present invention. It is preferable, however, that the polyisocyanate be a diisocyanate. Furthermore, although both aliphatic and aromatic polyisocyanates are within the contemplation of the present invention, it is preferred that the polyisocyanate be an aliphatic polyisocyanate. Thus, in a particularly preferred embodiment, the polyisocyanate is an aliphatic diisocyanate. Among particularly preferred aliphatic diisocyanates are isophorone diisocyanate, hexamet
Bechara Ibrahim
Chang Biau-Hung
Ilmenev Pavel
Cain Edward J.
Crompton Corporation
Reitenbach Daniel
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