Mixable room temperature castable polyurethane system

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From reactant having at least one -n=c=x group as well as...

Reexamination Certificate

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C528S063000, C528S064000, C528S067000

Reexamination Certificate

active

06420509

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates to an improved polyurethane compound which has utility as a potting compound in fan exit guide vane assemblies of commercial gas turbine engines.
Polyurethane compounds have been used as potting compounds in fan exit guide vane assemblies of commercial gas turbine engines. Currently available polyurethane potting materials suffer from a number of deficiencies. For example, some are difficult to process, resulting in high rework and/or poor yield. Others contain hazardous materials which require special handling procedures and which can not be used at all at many Manufacturing facilities.
One polyurethane compound which has been used is one from a company named Jonal. The compound is difficult to work with, as i t requires heating of the resin above 180 degrees Fahrenheit and melting of the hardener above 300 degrees Fahrenheit, before mixing. The combining of the two heated components is done by weight and a hand measured mark on the delivery system cartridge, which introduces mix variations. Once combined, the system has a working life of eight minutes. The hand mixing introduces another variable into the system along with entrapped air that cannot be removed in the short work-life time. The entrapped air bubbles are cause for vane assembly rejection/rework.
Thus, there remains a need for a polyurethane compound which has improved quality, manufacturing properties and adhesive strength.
It is the aim of the present invention to provide a polyurethane compound which fulfills this need.
SUMMARY OF THE INVENTION
Accordingly, it is an object of the present invention to provide a polyurethane compound which has improved quality, manufacturing properties and adhesive strength.
It is a further object of the present invention to provide a polyurethane compound as above which has utility as a potting compound in fan exit guide vane assemblies of commercial gas turbine engines.
It is a further object of the present invention to provide a polyurethane compound as above which can be mixed in manufacturing friendly automated equipment.
It is yet a further object of the present invention to provide a polyurethane compound as above which can be packaged without the introduction of air.
The polyurethane compound of the present invention meets the foregoing objects.
In accordance with the present invention, a polyurethane compound or system is provided which contains a formulation of polyurethane prepolymers mixed with an aromatic amine curing agent in a volumetric mix ratio of from about 0.9:1 to about 1:1. The formulation of polyurethane prepolymers consists of a blend of different polyethers based on diphenylmethane diisocyanate or, in other words, a blend of prepolymers made from polyethers and diphenylmethane diisocyanate. The aromatic amine curing agent preferably comprises a blend of oligomeric diamines and an aromatic diamine with a catalytic component. Both of the blends, when in an uncured state, are liquid at room temperature. Polyether type prepolymers are important for moisture and solvent resistance. Polyurethane based MDI prepolymers or MDI polyurethane prepolymers are important for health and safety reasons, for being liquid at room temperature, and for offering better adhesion properties. Aromatic amine curing is important for best thermal stability and moisture resistance.
Other details of the polyurethane compound of the present invention, as well as other objects and advantages attendant thereto, are set forth in the following detailed description.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT(S)
In accordance with the present invention, a preferred polyurethane compound is formed by mixing a formulation of polyurethane prepolymers with an aromatic amine curing agent in a volumetric mix ratio of about 0.9:1 to an about 1:1, preferably from about 0.95:1 to about 1:1.
The polyurethane prepolymer formulation in accordance with the present invention consists of a blend of different polyethers based on diphenylmethane diisocyanate (MDI), which blend has an NCO content in the range of about 11.5% to about 14.5%, preferably from about 12% to 14%, and most preferably about 13%. As used herein, the term NCO content means the grams of NCO per gram of prepolymer.
A polyether based MDI prepolymer to be used in the present invention should have a structure as follows:
where x≧1 and n has a repeat value of 0 to 4, preferably 1 to 2.
There are any number of commercially available materials that meet the foregoing structure. Suitable polyether based MDI prepolymers include Versathane SME-75A, Versathane SME-80A, Versathane SME-90A, Versathane SME-95A, and QG 162 (all manufactured by Air Products Corporation), Rubinate 9009 and Rubinate 1027 (both produced by ICI), Vibrathane B-625, Vibrathane B-635, Vibrathane B-670 and Vibrathane B-836 (all produced by Uniroyal), and Andur M-10.
The different polyethers which are used to form the blend preferably comprise two types of diphenylmethane diisocyanates. The first type of polyether has a NCO content in the range of from about 13.5% to about 16.5%, preferably in the range of from about 14% to about 16%, and most preferably about 15%, a density of about 1.2 g/cm
3
, and an equivalent weight of about 286 g/mol. Equivalent weight is the molecular weight divided by the number of reactive sites or equivalents on the prepolymer. One such material which may be used for the first type of polyether is Andur M-10. The second type of polyether has a NCO content in the range of from about 9.7% to about 12.7%, preferably from about 10.2% to about 12.2%, and most preferably about 11.2%, a density of about 1.06 g/cm
3
, and an equivalent weight of about 375 g/mol. One such suitable material which may be used for the second type of polyether is Vibrathane B-670.
The polyurethane prepolymer formulation is prepared by combining the two polyether types at room temperature, stirring them to obtain a homogeneous solution, de-aerating at room temperature, and handling using standard dry conditions for moisture sensitive urethanes. The two polyethers are mixed in volumetric amounts sufficient to provide the resulting blend with a NCO content in the range of about 11.5% to about 14.5%, preferably about 12% to 14% and most preferably about 13%. When using the aforementioned representative materials, 61.6 g of Andur M-10 may be mixed with 68.4 g of Vibrathane B-670 to form a useful polyether blend.
The aromatic amine curing agent (hardener) is formed from two oligomeric aromatic diamines (that is, polyether polymers terminated with aromatic amines) and a third aromatic diamine. The oligomeric aromatic diamines used in the present invention have a structure such as:
Suitable aromatic amines which may be used in the present invention include Versalink P-250, Versalink P-650, Versalink P-1000, Polacure 740M and Lonzacure MCDEA (all manufactured by Air Products) and Unilink 4100 and Unilink 4200 (both manufactured by UOP). The desired amine to NCO Stiochiometric ratio is between about 0.85:1 and about 1.05:1, preferably from about 0.9:1 to about 1:1, and ideally about 0.95:1.
The first of the oligomeric diamines to be used to form the curing agent preferably has a density of about 1.04 g/cm
3
and an equivalent weight of about 235 g/mol. A suitable oligomeric diamine which can be used for the first oligomeric diamine is Versalink P250. The second of the oligomeric diamines to be used to form the curing agent preferably has a density of about 1.04 g/cm
3
and an equivalent weight of about 415 g/mol. Versalink P250 has an average repeat value of n=3.5. A suitable oligomeric diamine which can be used for the second oligomeric diamine is Versalink P650. Versalink P650 has an average repeat value of n =9.5. The third aromatic diamine to be used to form the curing agent is preferably characterized by chlorine groups attached to it and has a density of about 0.95 g/cm
3
and an equivalent weight of about 190 g/mol. The chemical structure for this aromatic diamine is:
A suitable material for use as th

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