Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From phenol – phenol ether – or inorganic phenolate
Reexamination Certificate
2002-07-25
2004-08-31
Hightower, P. Hampton (Department: 1711)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
From phenol, phenol ether, or inorganic phenolate
C528S125000, C528S126000, C528S128000, C528S172000, C528S173000, C528S079000, C528S183000, C528S188000, C528S220000, C528S229000, C528S350000, C528S351000, C528S353000, C525S419000, C525S420000, C525S422000, C525S432000, C524S600000, C524S602000, C524S606000, C427S256000, C427S384000, C264S257000, C264S258000, C264S331120, C264S331210
Reexamination Certificate
active
06784276
ABSTRACT:
ORIGIN OF INVENTION
The invention described herein was made by an employee of the United States Government and may be manufactured and used by or for the Government for governmental purposes without the payment of any royalties thereon or therefor.
BACKGROUND OF INVENTION
1. Field of the Invention
This invention relates to stable solutions of polyimide precursors (monomers) having a solids content ranging from about 80 to 98 percent by weight, preferably 85-98% of the precursors in lower molecular weight alcohols. The concentrated solutions of polyimide precursors comprise effective amounts of aromatic dianhydrides, aromatic diamines and reactive crosslinkable monofunctional endcaps. More specifically, the concentrated solutions of polyimide precursors comprises a mixture of lower alkyl di- and/or mono-esters of an aromatic dianhydride, aromatic diamines, and monofunctional endcaps. The endcaps include monofunctional amines, monofunctional anhydrides, and alkyl monester-acids or alkyl diesters of monofunctional anhydrides wherein the lower alkyl groups have 1 or 2 carbons, e.g. the alkyl esters are derived from low molecular weight aliphatic alcohols such as methyl and ethyl alcohol. The high-solid monomer or precursor solutions solidify at room temperature, and essentially immobilize all the monomer reactants preventing the aging process of the monomer solution induced by chemical reactions. The solid monomer solution can be stored and shipped at room temperature with unlimited shelf-life, eliminating the need of shipping these monomer solutions with dry ice. Prepregs are prepared by impregnating fibrous materials e.g. carbon and glass fibers with effective amounts of the highly concentrated stable solutions of the polyimide precursors.
2. Description of Related Prior Art
Polymerization of Monomer Reactants (PMR) to obtain polyimides is a class of high performance composite resins. Polyimide graphite fiber-reinforced composites are increasingly used in various aircraft engine components, which operate at temperatures ranging up to 371° C. for thousands of hours. For example, PMR-15 is one of the best known and most widely used PMR polyimide. PMR-15 attributes include relatively easy processing, substantially lower costs, and excellent property retention at elevated temperatures, compared to other commercially available high temperature resin materials.
The preparation of polyimides from mixtures of monomeric diamines and esters of polycarboxylic acids is disclosed, for example, in U.S. Pat. No. 3,745,149. Patentee disclosed that polyimides can be processed from a mixture of monomeric reactants using lower alcohols to esterify an anhydride endcap and an aromatic dianhydride. These monomeric reactants when combined with an aromatic diamine in the molar ration, of N diester-diacid/N+1 diamine/2 ester-acid endcap, form a monomeric mixture which at high temperature polymerizes to a polyimide. This procedure was the evolution of the terminology PMR (polymerization of monomeric reactants).
More specifically, U.S. Pat. No. 3,745,149 discloses the use of a 50-70% solid content of monomer reactants in methanol which has to be stored in the freezer and overnight shipped in dry ice to prevent the aging process generated by the chemical reactions among the monomers that occur at room temperature. During the prepreg production by the hot-melt process, a 50% monomer solution is concentrated by boiling off the excess methanol under vacuum. The heating of monomer solutions in methanol promotes the reactions among the monomer reactants and essentially accelerated the aging process. This extra step also requires additional labor cost. As a result, prepregs produced by the hot-melt process from a 50-70% solid content in liquid form exhibited less resin mobility during the processing of prepreg laminates into composites. A more recent modification discloses the use of isopropyl alcohol to make the corresponding ester-acids to extend the shelf-life of monomer reactants. However, isopropanol (boiling point of 82.4° C., heat of vaporization=39.85 Kjoul/mol) as a solvent is more difficult to remove than either ethanol (BP=78° C., heat of vaporization=38.6 Kjoul/mol) or methanol (BP=64.7° C., heat of vaporization=35.21 Kjoul/mol) during laminate processing. Upon imidization, the use of isopropyl ester-acids as the monomer reactants will loose more weight due to the evaporation of isopropanol as compared to other alcohols (MW of isopropanol=60 g/mol, ethanol=46 g/mole, methanol=32 g/mol), thus yielding lower resin content in the composites compared to either the ethyl ester or methyl ester.
A major disadvantage of the state-of-the-art PMR technology, as practiced commercially today, is the limited shelf life of the monomeric solutions at room temperatures, the short working outlife time, and an extremely high sensitivity toward premature aging at temperatures even slightly above room temperature. The disadvantages cause premature polymerization during all phases of PMR usage such as in synthesis, manufacturing, shipping, handling, storage, and fabrication layup/processing. Moreover, the 50-70% monomer solutions are difficult to adapt to low-cost manufacturing processes such as resin transfer molding (RTM) due to the large quantity of solvent that needs to be removed.
The present answer to premature aging of PMR solutions and the preparation of prepregs has been through rigorous handling requirements via strict manufacturing temperature control, over-night air shipment in dry ice, freezer storage of PMR materials, stringent quality control governing allowed outlife usage time, and freezer storage time which significantly adds to the final cost of PMR composites. In comparison, the high-solids polyimide precursor monomer solution of this invention is based on a process that significantly retards aging of the PMR solutions and PMR prepregs, rather than being based on the rigid temperature controls as evolved and practiced in present PMR technology. Moreover, the instant process extends to other manufacturing processes such as solvent assisted RTM and resin infusion.
SUMMARY OF THE INVENTION
This invention relates to stable solutions of polyimide precursors (monomers) having a solids content ranging from about 80 to 98 percent and preferably from 85 to 98% by weight of said polyimide precursors in lower molecular weight alcohols i.e. aliphatic alcohols having 1 or 2 carbon atoms. The concentrated solutions of the polyimide precursors comprise effective amounts of at least one aromatic diamine, at least one dianhydride selected from the group consisting of aromatic dianhydrides and lower alkyl ester-acids i.e. mono and dialkyl esters of aromatic dianhydrides wherein the alkyl ester groups have 1 or 2 carbon atoms, and at least one mono functional endcap selected from the group consisting of aromatic monoamines, aromatic monoanhydrides and alkyl esters of monoanhydrides wherein the alkyl ester groups have 1 or 2 carbons. Prepregs are prepared with these highly concentrated solutions by directly impregnating a fibrous material such as carbon or glass fibers to obtain high temperature polyimide composites for use in structural materials in military and civil applications such as jet engine cowls and ducts because of the light-weight, load-bearing characteristics and stability at high temperatures.
Accordingly, it is an object of this invention to improve the stability and shelf-life of polyimide precursor (monomer) solutions by providing highly concentrated solutions which arc not sensitive to premature aging at room temperature.
It is another object of this invention to provide highly concentrated polyimide precursor solutions for use in preparing polyimide prepregs.
It is still another object of this invention to provide a stable mixture of polyimide precursors at high concentrations in low molecular weight alcohols for use in the preparation of PMR prepregs.
It is a further object of this invention to provide highly concentrated solutions of poly
Hampton Hightower P.
Stone Kent N.
The United States of America as represented by the United States
Tura James V.
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