Patent Application
20130171395
This disclosure relates to filled polyimide resin compositions that are useful for high temperature applications that require high thermal oxidative stability, such as aircraft engine parts.
The unique performance of polyimide compositions under stress and at high temperatures have made them useful in applications requiring high thermal oxidative stability. Some examples of such applications are aircraft engine parts, aircraft wear pads, automatic transmission bushings and seal rings, tenter frame pads and bushings, material processing equipment parts, and pump bushings and seals.
Despite the variety of polyimide compositions, and additives for those compositions such as graphite, that have previously been available, a need still remains for polyimide compositions that exhibit as molded parts the desirably high degree of thermal oxidative stability currently required for applications such aircraft engine parts, while maintaining the other advantageous attributes of the polyimide material.
Disclosed herein are compositions comprising in admixture (a) an aromatic polyimide in an amount of about 30 weight parts to about 90 weight parts; (b) acid-washed kaolinite in an amount of about 0.5 weight parts to about 10 weight parts; and (c) graphite in an amount of about 0 weight parts to about 60 weight parts; wherein all weight parts combined together total to 100 weight parts.
Three dimensional articles comprising these compositions are also provided.
Disclosed herein are compositions that contain (a) an aromatic polyimide in an amount of about 30 weight parts to about 90 weight parts; (b) acid-washed kaolinite in an amount of about 0.5 weight to about 12 weight parts; and (c) graphite in an amount of about 0 weight parts to about 60 weight parts; where weight parts (a), (b), and (c) combined together total to 100 weight parts.
A polyimide as used as the component “(a)” in a composition hereof is a polymer in which at least about 80%, preferably at least about 90%, and more preferably essentially all (e.g. at least about 98%) of the linking groups between repeat units are imide groups. An aromatic polyimide as used herein includes an organic polymer in which about 60 to about 100 mol %, preferably about 70 mol % or more, and more preferably about 80 mol % or more of the repeating units of the polymer chain thereof have a structure as represented by the following Formula (I):
wherein R1 is a tetravalent aromatic radical and R2 is a divalent aromatic radical, as described below.
An aromatic polyimide as used herein is preferably a rigid aromatic polyimide. A polyimide polymer is considered rigid when there are no, or an insignificant amount (e.g. less than about 10 mol %, less than about 5 mol %, less than about 1 mol % or less than about 0.5 mol %) of, flexible linkages in the polyimide repeating unit. Flexible linkages are moieties that are predominantly composed of a small number of atoms, and that have an uncomplicated structure (such as straight-chain rather than branched or cyclic), and thus permit the polymer chain to bend or twist with relative ease at the location of the linkage. Examples of flexible linkages include without limitation: —O—, —N(H)—C(O)—, —S—, —SO2—, —C(O)—, —C(O)—O—, —C(CH3)2—, —C(CF3)2—, —(CH2)—, and —NH(CH3)—.
A polyimide polymer suitable for use herein may be synthesized, for example, by reacting a monomeric aromatic diamine compound (which includes derivatives thereof) with a monomeric aromatic tetracarboxylic acid compound (which includes derivatives thereof), and the tetracarboxylic acid compound can thus be the tetracarboxylic acid itself, the corresponding dianhydride, or a derivative of the tetracarboxylic acid such as a diester diacid or a diester diacidchloride. The reaction of the aromatic diamine compound with an aromatic tetracarboxylic acid compound produces the corresponding polyamic acid (“PAA”), amic ester, amic acid ester, or other reaction product according to the selection of starting materials. An aromatic diamine is typically polymerized with a dianhydride in preference to a tetracarboxylic acid, and in such a reaction a catalyst is frequently used in addition to a solvent. A nitrogen-containing base, phenol or an amphoteric material can be used as such a catalyst.
A polyamic acid, as a precursor to a polyimide, can be obtained by polymerizing an aromatic diamine compound and an aromatic tetracarboxylic acid compound, preferably in substantially equimolar amounts, in an organic polar solvent that is generally a high-boiling solvent such as pyridine, N-methylpyrrolidone, dimethylacetamide, dimethylformamide or mixtures thereof. The amount of all monomers in the solvent can be in the range of about 5 to about 40 wt %, in the range of about 6 to about 35 wt %, or in the range of about 8 to about 30 wt %, based on the combined weight or monomers and solvent. The temperature for the reaction is generally not higher than about 100° C., and may be in the range of about 10° C. to 80° C. The time for the polymerization reaction generally is in the range of about 0.2 to 60 hours.
Imidization to produce the polyimide, i.e. ring closure in the polyamic acid, can then be effected through thermal treatment (e.g. as described in U.S. Pat. No. 5,886,129), chemical dehydration or both, followed by the elimination of a condensate (typically, water or alcohol). For example, ring closure can be effected by a cyclization agent such as pyridine and acetic anhydride, picoline and acetic anhydride, 2,6-lutidine and acetic anhydride, or the like.
In various embodiments of the thus-obtained polyimide, about 60 to 100 mole percent, preferably about 70 mole percent or more, more preferably about 80 mole percent or more, of the repeating units of the polymer chain thereof have a polyimide structure as represented by the following Formula (I):
wherein R1 is a tetravalent aromatic radical derived from the tetracarboxylic acid compound; and R2 is a divalent aromatic radical derived from the diamine compound, which may typically be represented as H2N—R2—NH2.
A diamine compound as used to prepare a polyimide for a composition hereof may be one or more of the aromatic diamines that can be represented by the structure H2N—R2—NH2, wherein R2 is a divalent aromatic radical containing up to 16 carbon atoms and, optionally, containing one or more (but typically only one) heteroatoms in the aromatic ring, a heteroatom being, for example, selected from —N—, —O—, or —S—. Also included herein are those R2 groups wherein R2 is a biphenylene group. Examples of aromatic diamines suitable for use to make a polyimide for a composition hereof include without limitation 2,6-diaminopyridine, 3,5-diaminopyridine, 1,2-diaminobenzene, 1,3-diaminobenzene (also known as m-phenylenediamine or “MPD”), 1,4-diaminobenzene (also known as p-phenylenediamine or “PPD”), 2,6-diaminotoluene, 2,4-diaminotoluene, naphthalenediamines, and benzidines such as benzidine and 3,3′-dimethylbenzidine. The aromatic diamines can be employed singly or in combination. In one embodiment, the aromatic diamine compound is 1,4-diaminobenzene (also known as p-phenylenediamine or “PPD”), 1,3-diaminobenzene (also known as m-phenylenediamine or “MPD”), or mixtures thereof.
Aromatic tetracarboxylic acid compounds suitable for use to prepare a polyimide for a composition hereof may include without limitation aromatic tetracarboxylic acids, acid anhydrides thereof, salts thereof and esters thereof. An aromatic tetracarboxylic acid compound may be as represented by the general Formula (II):
wherein R1 is a tetravalent aromatic group and each R3 is independently hydrogen or a lower alkyl (e.g. a normal or branched C1˜C10, C1˜C8, C1˜C6 or C1˜C4) group. In various embodiments, the alkyl group is a C1 to C3 alkyl group. In various embodiments, the tetravalent organic group R1 may have a structure as represented by one of the following formulae:
Examples of suitable aromatic tetracarboxylic acids include without limitation 3,3′,4,4′-biphenyltetracarboxylic acid, 2,3,3′,4′-biphenyltetracarboxylic acid, pyromellitic acid, 2,3,6,7-naphthalenetetracarboxylic acid, and 3,3′,4,4′-benzophenonetetracarboxylic acid. The aromatic tetracarboxylic acids can be employed singly or in combination. In one embodiment, the aromatic tetracarboxylic acid compound is an aromatic tetracarboxylic dianhydride. Examples include without limitation 3,3′,4,4′-biphenyltetracarboxylic dianhydride (“BPDA”), pyromellitic dianhydride (“PMDA”), 3,3,4,4′-benzophenonetetracarboxylic dianhydride, 1,4,5,8-naphthalenetetracarboxylic dianhydride, 2,3,6,7-naphthalenetetracarboxylic dianhydride, 1,4,5,8-naphthalenetetracarboxylic acid, 2,3,6,7-naphthalenetetracarboxylic acid, and mixtures thereof.
In one embodiment of a composition hereof, a suitable polyimide polymer may be prepared from 3,3′,4,4′-biphenyltetracarboxylic dianhydride (“BPDA”) as the aromatic tetracarboxylic acid compound, and from a mixture of p-phenylenediamine (“PPD”) and m-phenylenediamine (“MPD”) as the aromatic diamine compound. In one embodiment, the aromatic diamine compound is greater than 60 to about 85 mol % p-phenylenediamine and 15 to less than 40 mol % m-phenylenediamine. Such a polyimide is described in U.S. Pat. No. 5,886,129 (which is by this reference incorporated in its entirety as a part hereof for all purposes), and the repeat unit of such a polyimide may also be represented by the structure shown generally in the following Formula (III):
wherein greater than 60 to about 85 mol % of the R2 groups are p-phenylene radicals:
and 15 to less than 40 mol % are m-phenylene radicals:
In an alternative embodiment, a suitable polyimide polymer may be prepared from 3,3′,4,4′-biphenyltetracarboxylic dianhydride (“BPDA”) as a dianhydride derivative of the tetracarboxylic acid compound, and 70 mol % p-phenylenediamine and 30 mol % m-phenylenediamine as the diamine compound.
A polyimide as used herein is preferably an infusible polymer, which is a polymer that does not melt (i.e. liquefy or flow) below the temperature at which it decomposes. Typically, parts prepared from a composition of an infusible polyimide are formed under heat and pressure, much like powdered metals are formed into parts (as described, for example, in U.S. Pat. No. 4,360,626, which is by this reference incorporated as a part hereof for all purposes).
A polyimide as used herein preferably has a high degree of stability to thermal oxidation. At elevated temperature, the polymer will thus typically not undergo combustion through reaction with an oxidant such as air, but will instead vaporize in a thermolysis reaction.
An acid-washed kaolinite filler is used as the component “(b)” in a composition hereof. Kaolinite is a sheet-type silicate whose molecules are arranged in two sheets or plates, one of silica and one of alumina. Kaolinite is a clay mineral with the chemical composition Al2Si2O5(OH)4. It is a layered silicate mineral, with one tetrahedral sheet linked through oxygen atoms to one octahedral sheet of alumina octahedra. Rocks that are rich in kaolinite are known as china clay or kaolin. In contrast, smectites such as montmorillonite clay minerals are arranged in two silica sheets and one alumina sheet. The molecules of the smectites are less firmly linked together than those of the kaolinite group and are thus further apart. Maintaining the phase stability of crystal structure of the sheet silicates is desirable, as is maintaining the thermal stability of the structural water of the sheet silicates at higher temperatures, such as up to about 450° C. [as shown, for example, by thermogravimetric analysis (TGA)]. Loss of structural water during processing of a polyimide composition can result in harm to polyimide integrity, and possibly change the crystal structure of the sheet silicate, giving a harder, more abrasive compound. Examples of sheet silicates that are not stable enough to be included in the compositions described herein are montmorillonite, vermiculite, and pyrophyllite. Kaolinite is discussed further in Murray, Applied Clay Science 17 (2000) 207-221.
A kaolinite as used in a composition hereof is washed in an acid such as an inorganic acid (e.g. aqueous HCl) or a low molecular weight organic acid (e.g. oxalic acid, citric acid, or malic acid). It has been found that, a low molecular weight organic acid, such as oxalic, citric or malic acid, can attack (dissolve) kaolinite more rapidly that an inorganic acid at a selected pH. Oxalic acid attacks more rapidly than citric acid, and citric acid attacks more rapidly than malic acid [X. Wang et al, Journal of Colloid and Interface Science 290 (2005) 481-488; E. Wieland and W. Stumm, Geochimica et Cosmochimica Acta, 56(9) (1992), 3339-3355]. The kaolinite undergoing acid-washing can be contacted with acid as received. Alternatively, the kaolinite can, for example, be ground or sonicated to disaggregate clumps prior to contact with the acid. The acid-wash treatment is carried out at an acid concentration preferably giving a solution with pH lower than 6; at an acid to kaolinite concentration sufficient for good mixing of the solution; at temperatures ranging from room temperature to reflux conditions of about 104° C.; and over a time period ranging from about 1 h to several days. The optimum time/temperature/acid type/acid concentration combination will depend on factors of the specific situation such as particle size and/or operational scale, and is readily determined.
Graphite is used as the component “(c)” of a composition hereof. Graphite is typically added to a polyimide composition to improve wear and frictional characteristics, and to control the coefficient of thermal expansion (CTE). The amount of graphite used in a polyimide composition for such purpose is thus sometimes advantageously chosen to match the CTE of the mating components.
Graphite is commercially available in a variety of forms as a fine powder, and may have a widely varying average particle size that is, however, frequently in the range of from about 5 to about 75 microns. In one embodiment, the average particle size is in the range of from about 5 to about 25 microns. In another embodiment, graphite as used herein contains less than about 0.15 weight percent of reactive impurities, such as those selected from the group consisting of ferric sulfide, barium sulfide, calcium sulfide, copper sulfide, barium oxide, calcium oxide, and copper oxide.
Graphite as suitable for use herein can be either naturally occurring graphite or synthetic graphite. Natural graphite generally has a wide range of impurity concentrations, while synthetically produced graphite is commercially available having low concentrations of reactive impurities. Graphite containing an unacceptably high concentration of impurities can be purified by any of a variety of known treatments including, for example, chemical treatment with a mineral acid. Treatment of impure graphite with sulfuric, nitric or hydrochloric acid, for example, at elevated or reflux temperatures can be used to reduce impurities to a desired level.
The acid-washed kaolinite, component (b), and graphite, component (c), as used in the compositions and articles hereof, are frequently incorporated into the heated solvent prior to transfer of the PAA polymer solution as described above, so that the resulting polyimide is precipitated in the presence of the components (b) and (c), which thereby become incorporated into the composition.
In the compositions of this invention, the content of the various components includes all of the formulations in which the compositional content may be expressed by any combination of the various maxima and minima, as set forth below, for any one component of the composition together with any such combination of maxima and minima for either or both of the other two components, viz:
In a composition hereof, the amounts of the respective weight parts of the three components as combined together in any particular formulation, taken from the ranges as set forth above, will total to 100 weight parts. In embodiments where graphite is present in an amount of 0 weight parts, the composition is formulated in the absence of graphite, which is excluded, and the weight parts of the component (a), a polyimide, and the component (b), an acid-washed kaolinite, will total to 100 weight parts.
In certain embodiments of the compositions hereof, component (a) is present in an amount between about 30 and about 80 weight parts; component (b) is present in an amount between about 0.5 and about 12 weight parts; and component (c) is present in an amount between about 0 and about 60 weight parts.
In other embodiments of the compositions hereof, component (a) is present in an amount between about 40 and about 70 weight parts; component (b) is present in an amount between about 0.5 and about 10 weight parts; and component (c) is present in an amount between about 0 and about 60 weight parts.
In yet other embodiments of the compositions hereof, component (a) is present in an amount between about 40 and about 70 weight parts; component (b) is present in an amount between about 1 and about 10 weight parts; and component (c) is present in an amount between about 5 and about 50 weight parts.
In yet other embodiments of the compositions hereof, component (a) is present in an amount between about 40 and about 70 weight parts; component (b) is present in an amount between about 1 and about 8 weight parts; and component (c) is present in an amount between about 5 and about 50 weight parts.
One or more additives may be used as an optional component “(d)” of a composition hereof. When used, additive(s) may be used in an amount in the range of about 5 to about 70 wt % based on the total weight of all four components together in a 4-component [(a)+(b)+(c)+(d)] composition, with the total weight of three components together in a 3-component [(a)+(b)+(c)] composition being in the range of about 30 to about 95 wt % based on the total weight of all four components together in a 4-component [(a)+(b)+(c)+(d)] composition.
Additives suitable for optional use in a composition hereof may include, without limitation, one or more of the following: pigments; antioxidants; materials to impart a lowered coefficient of thermal expansion, e.g. carbon fibers; materials to impart high strength properties e.g. glass fibers, ceramic fibers, boron fibers, glass beads, whiskers, graphite whiskers or diamond powders; materials to impart heat dissipation or heat resistance properties, e.g. aramid fibers, metal fibers, ceramic fibers, whiskers, silica, silicon carbide, silicon oxide, alumina, magnesium powder or titanium powder; materials to impart corona resistance, e.g. natural mica, synthetic mica or alumina; materials to impart electric conductivity, e.g. carbon black, silver powder, copper powder, aluminum powder or nickel powder; materials to further reduce wear or coefficient of friction, e.g. boron nitride or poly(tetrafluoroethylene) homopolymer and copolymers. Fillers may be added as dry powders to the final resin prior to parts fabrication.
Disclosed herein are parts and other three-dimensional articles (as opposed, for example, to coatings or films) comprising a composition hereof. By a “part” is meant a three-dimensional shaped object, that may be a final shape that is useful directly, or a “preform”, “blank” or “standard shape” that will be cut and/or machined into its final shape. As with products made from other infusible polymeric materials, parts fabricated from a composition hereof may be made by techniques involving the application of heat and pressure (see, for example, U.S. Pat. No. 4,360,626). Suitable conditions may include, for example, pressures in the range of from about from 50,000 to 100,000 psi (345 to 690 MPa) at ambient temperatures. Physical properties of articles molded from a composition hereof can be further improved by sintering, which may typically be performed at a temperature in the range of from about 300° C. to about 450° C.
Parts and other articles prepared from a composition hereof exhibit improved thermal oxidative stability over comparable compositions that do not comprise acid-washed kaolinite and are useful in, for example, aerospace, transportation, and materials handling and processing equipment applications.
Articles prepared from a composition hereof are useful in aerospace applications such as aircraft engine parts, such as bushings (e.g., variable stator vane bushings), bearings, washers (e.g., thrust washers), seal rings, gaskets, wear pads, splines, wear strips, bumpers, and slide blocks. These aerospace application parts may be used in all types of aircraft engines such as reciprocating piston engines and, particularly, jet engines. Other examples of aerospace applications include without limitation: turbochargers; shrouds, aircraft subsystems such as thrust reversers, nacelles, flaps systems and valves, and aircraft fasteners; airplane spline couplings used to drive generators, hydraulic pumps, and other equipment; tube clamps for an aircraft engine to attach hydraulic, hot air, and/or electrical lines on the engine housing; control linkage components, door mechanisms, and rocket and satellite components.
Articles prepared from a composition hereof are also useful in transportation applications, for example, as components in vehicles such as but not limited to automobiles, recreational vehicles, off-road vehicles, military vehicles, commercial vehicles, farm and construction equipment and trucks. Examples of vehicular components include without limitation: automotive and other types of internal combustion engines; other vehicular subsystems such as exhaust gas recycle systems and clutch systems; fuel systems (e.g., bushings, seal rings, band springs, valve seats); pumps (e.g., vacuum pump vanes); transmission components (e.g., thrust washers, valve seats, and seal rings such as seal rings in a continuously variable transmission), transaxle components, drive-train components, non-aircraft jet engines; engine belt tensioners; rubbing blocks in ignition distributors; powertrain applications (e.g., emission components, variable valve systems, turbochargers (e.g., ball bearing retainers, wastegate bushings), air induction modules); driveline applications (e.g., seal rings, thrust washers and fork pads in manual and dual clutch transmissions, transfer cases); seal rings and thrust washers for heavy-duty off-road transmissions and hydraulic motors; bushings, buttons, and rollers for continuous variable transmissions in all-terrain vehicles (“ATVs”) and snowmobiles; and chain tensioners for snowmobile gear cases; brake systems (e.g., wear pads, valve components for anti-lock braking systems); door hinge bushings; gear stick rollers; wheel disc nuts, steering systems, air conditioning systems; suspension systems; intake and exhaust systems; piston rings; and shock absorbers.
Articles prepared from a composition hereof are also useful in material handling equipment and materials processing equipment, such as injection molding machines and extrusion equipment (e.g., insulators, seals, bushings and bearings for plastic injection molding and extrusion equipment), conveyors, belt presses and tenter frames; and films, seals, washers, bearings, bushings, gaskets, wear pads, seal rings, slide blocks and push pins, glass handling parts such as clamps and pads, seals in aluminum casting machines, valves (e.g., valve seats, spools), gas compressors (e.g., piston rings, poppets, valve plates, labyrinth seals), hydraulic turbines, metering devices, electric motors (e.g., bushings, washers, thrust plugs), small-motor bushings and bearings for handheld tools appliance motors and fans, torch insulators, and other applications where low wear is desirable.
Articles prepared from a composition hereof are also useful in the manufacture of beverage cans, for example, bushings in body makers that form the can shape, vacuum manifold parts, and shell press bands and plugs; in the steel and aluminum rolling mill industry as bushings and mandrel liners; in gas and oil exploration and refining equipment; and in textile machinery (e.g., bushings for weaving machines, ball cups for knitting looms, wear strips for textile finishing machines).
In some applications, an article prepared from a composition hereof is in contact with metal at least part of the time when the apparatus in which it resides is assembled and in normal use.
The advantageous attributes and effects of the compositions hereof may be seen in the examples (Examples 1 and 2) as described below. The embodiments of the composition on which the examples are based are representative only, and the selection of those embodiments to illustrate the invention does not indicate that materials, components, reactants, ingredients, formulations or specifications not described in these examples are not suitable for practicing the inventions herein, or that subject matter not described in these examples is excluded from the scope of the appended claims and equivalents thereof. The significance of these examples is better understood by comparing the results obtained therefrom with the results obtained from certain trial runs that are designed to serve as controlled experiments (Comparative Examples A˜D) and provide a basis for such comparison since the compositions therein do not contain the kaolinite.
In the examples, the following abbreviations are used: “BPDA” is defined as 3,3′,4,4′-biphenyltetracarboxylic anhydride, “DI” is defined as deionized, “g” is defined as gram(s), “mL” is defined as milliliter(s), “mmol” is defined as millimole(s), “MPa” is defined as megapascal(s), “MPD” is defined as m-phenylenediamine, “nm” is defined as nanometer(s), “μm” is defined as micrometer(s), “PPD” is defined as p-phenylenediamine, “psi” is defined as pounds per square inch, “TOS” is defined as thermal oxidative stability, and “wt %” is defined as weight percent(age).
3,3′,4,4′-biphenyltetracarboxylic anhydride was obtained from Mitsubishi Gas Chemical Co., Inc. (Tokyo, Japan). M-phenylenediamine and p-phenylenediamine were obtained from DuPont (Wilmington, Del., USA). The graphite used was a synthetic graphite, maximum 0.05% ash, with a median particle size of about 8 μm. Polyfil® DL kaolinite was purchased from J.M. Huber Corporation, (Atlanta, Ga., USA). Polyfil® DL is a large particle size (about 1 μm), water-washed clay which is processed to have a high aspect ratio; the clay stacks are delaminated, reduced to thin platelets.
Dried polyimide resin was fabricated into tensile bars for TOS measurements by direct forming according to ASTM E8 (2006), “Standard Tension Test Specimen for Powdered Metal Products-Flat Unmachined Tensile Test Bar”, at room temperature and 100,000 psi (690 MPa) forming pressure. The tensile bars were sintered at 405° C. for 3 hours with a nitrogen purge.
Acid-washed kaolinite was prepared by adding 50 grams of kaolinite clay and 250 mL of 0.15 M oxalic acid water (1.35 grams of oxalic acid in 1 L of DI water) into a 1000 mL two-neck round flask with a magnetic stirrer bar attached to a condenser and a thermocouple. The bottom of the round flask was placed inside a bath containing silicone fluid used for heating which was sitting on top of a stirrer/hot plate. A second thermocouple was inserted into the silicone fluid to read its temperature. The solution inside the flask was stirred and heat applied until the temperature of the silicone fluid reached 150° C. to 160° C. while the inside flask temperature reached 101° C. Reflux was maintained during a 4 hour period.
Once the solution cooled down to room temperature, it was slowly filtered using a 0.45 μm SFCA (surfactant-free cellulose acetate) filter device (Nalgene) attached to a house vacuum line until a moist cake remained at the top of the filter. The kaolinite cake and 250 mL of deionized water were added to a 500 mL glass bottle and shaken vigorously by hand to form a dispersion. The solution was filtered again. A small portion of the resulting kaolinite wet cake was then dried in a vacuum oven for two hrs for Inductively Couple Plasma (ICP) analysis. The remaining cake was dried in a nitrogen purged vacuum oven at 120° C. for 6 hrs. Once dried, it was ground using a mortar and pestle.
Alternatively, kaolinite can be sonicated prior to adding the oxalic acid. About 50 grams of kaolinite were sonicated in 80 mL of deionized water for 7 min using a Vibracell—VC 500 sonicator and a ½ inch horn that provided 50 Watts energy to the solution. The solution along 0.3375 grams oxalic acid and 170 mL of deionized water were transferred to a 1000 mL two-neck round flask containing a magnetic stirrer bar attached to a condenser and a thermocouple. Refluxing and filtration steps were carried out as described above.
Thermooxidative stability (TOS) was measured under 5 atmospheres of air (0.5 MPa) and weight loss after 25 hours at 800° F. (427° C.)
Polyimide resin based on 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA), m-phenylene diamine (MPD) and p-phenylene diamine (PPD) was prepared according to the method described in U.S. Pat. No. 5,886,129. Ingredients were 4.397 g MPD (40.7 mmol), 10.260 g (94.9 mmol) PPD, and 39.375 g (135.2 mmol) BPDA. The polyamic acid solution thereby produced (500 mL) was imidized in the presence of 1.86 g of acid-washed kaolinite, to produce a polyimide resin containing 4 wt % acid-washed kaolinite. The resin was isolated, washed, and dried. After drying, the resin was ground through a 20 mesh screen using a Wiley mill to form a powder.
Thermooxidative stability (TOS) was measured under 5 atmospheres of air (0.5 MPa) and weight loss after 25 hours at 800° F. (427° C.) is given in Table 1. This determination is an average of two measurements on the same batch of resin.
Polyimide resin based on 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA), m-phenylene diamine (MPD) and p-phenylene diamine (PPD) was prepared according to the method of Example 1, but in the absence of kaolinite. The TOS of the resulting resin is given in Table 1 and is the average of two measurements on the same batch of resin.
This resin was prepared by the method of Example 1, except as-received kaolinite was used in place of acid-washed kaolinite. The TOS of the resulting resin is given in Table 1 and is the average of two measurements on the same batch of resin.
Polyimide based on 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA), m-phenylene diamine (MPD) and p-phenylene diamine (PPD) was prepared according to the method described in U.S. Pat. No. 5,886,129. Ingredients were 8.77 g MPD (81.1 mmol), 20.47 g (189 mmol) PPD, and 79.55 g (270 mmol) BPDA. The BPDA was added to a pyridine solution of the MPD and PPD. The polyamic acid solution produced was imidized in the presence of 43.73 g of graphite and 0.89 g of predispersed, acid-washed kaolinite to produce a polymer containing 49 wt % graphite and 1 wt % kaolinite. To prepare predispersed kaolinite, acid-washed kaolinite and 250 mL of anhydrous pyridine were added to a wide mouth jar and sonicated for 30 sec, to form a suspension, after which the suspension was allowed to rest for 30 sec, followed by another 30 sec of sonication. The polymer was isolated, washed, and dried. After drying, the polymer was ground through a 20 mesh screen using a Wiley mill to form a powder.
The TOS of the resulting resin is given in Table 1 and is the average of two measurements on the same batch of resin.
This resin was prepared by the method of Example 2, except that no kaolinite was used in the preparation. The TOS of the resulting resin is given in Table 1 and is the average of fourteen resin batches.
This resin was prepared by the method of Example 2, except that the kaolinite used was not acid-washed. The TOS of the resulting resin is given in Table 1 and is the average of fourteen resin batches.
Where a range of numerical values is recited herein, the range includes the endpoints thereof and all the individual integers and fractions within the range, and also includes each of the narrower ranges therein formed by all the various possible combinations of those endpoints and internal integers and fractions to form subgroups of the larger group of values within the stated range to the same extent as if each of those narrower ranges was explicitly recited. Where a range of numerical values is stated herein as being greater than a stated value, the range is nevertheless finite and is bounded on its upper end by a value that is operable within the context of the invention as described herein. Where a range of numerical values is stated herein as being less than a stated value, the range is nevertheless bounded on its lower end by a non-zero value.
In this specification, unless explicitly stated otherwise or indicated to the contrary by the context of usage, where an embodiment of the subject matter hereof is stated or described as comprising, including, containing, having, being composed of or being constituted by or of certain features or elements, one or more features or elements in addition to those explicitly stated or described may be present in the embodiment. An alternative embodiment of the subject matter hereof, however, may be stated or described as consisting essentially of certain features or elements, in which embodiment features or elements that would materially alter the principle of operation or the distinguishing characteristics of the embodiment are not present therein. A further alternative embodiment of the subject matter hereof may be stated or described as consisting of certain features or elements, in which embodiment, or in insubstantial variations thereof, only the features or elements specifically stated or described are present.
In this specification, unless explicitly stated otherwise or indicated to the contrary by the context of usage,
This application claims priority under 35 U.S.C. §119(e) from, and claims the benefit of, U.S. Provisional Application No. 61/387,598, filed Sep. 29, 2010, which is by this reference incorporated in its entirety as a part hereof for all purposes.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US11/53958 | 9/29/2011 | WO | 00 | 3/13/2013 |
| Number | Date | Country | |
|---|---|---|---|
| 61387598 | Sep 2010 | US |
