Moisture and heat resistant coating for glass fibers

Abstract

A moisture and heat resistant finish coating for materials having a hydroxylated surface such as glass fibers embeddable in a resin matrix composite consisting essentially of approximately, by weight, 40-98 percent of a polyimide film former, 2-60 percent of a silane coupling agent and up to 30 percent of a wetting and lubricating agent.

Description

The present invention relates to a moisture and heat resistant coating for glass fibers and more particularly to a moisture and heat resistant finish coating for glass fibers comprising a mixture of a polyimide film former, a silane coupling agent and a wetting/lubricating agent.

In general, there are two major problems inhibiting successful usage of state-of-the-art composite materials made of resin reinforced with glass fibers such as glass/epoxy, glass/polyester and glass/polyimide. One of these problems is the occurrence of a slow decrease in mechanical properties, particularly in shear and flexural strength, which is exhibited after exposure to humid atmospheres for extended periods of time -- up to 5 years. This loss in mechanical strength on ambient aging reduces the reliability of any system containing these materials, particularly those which may require long time storage before use.

Although the prior art has used various starches, silanes and plastic materials as coatings in an effort to remedy the aforesaid deterioration, efforts have been less than successful. The coatings have been applied to glass fibers both from aqueous solutions and from organic solutions but, until the present invention, the fibers have not been able to consistently retain more than approximately 80 percent of their tensile strength after exposure to humid conditions or boiling water vapors.

The other major problem facing present day glass-resin composites is that of degradation after exposure to elevated temperatures of 500.degree. F and higher.

SUMMARY OF THE INVENTION

The present invention, in general, contemplates a moisture and heat resistant finish coating for objects having an hydroxylated surface and, more particularly, for glass fibers which are embeddable in a resin matrix. The finish coating contains as essential ingredients at least one polyimide film former and at least one coupling agent. In one embodiment, there is included, by weight, approximately, 40 -98 percent, preferably 45 -95 percent, of a polyimide film former. The term "polyimide film former", for the purposes of the present invention is defined to mean a resin material which, when applied as a solution to a surface, spreads out into a continuous film and, when the solvent evaporates, leaves a nonporous film coating and which resin material is selected from the group consisting of (1) a fully imidized and polymerized polyimide containing the repeating unit ##STR1## wherein R.sub.1 is a tetravalent radical selected from the group consisting of ##STR2## wherein X = O, S, SO.sub.2, CH.sub.2, ##STR3## and R.sub.2 is a divalent aromatic or aliphatic radical selected from the group consisting of ##STR4## and R.sub.3 is an aromatic divalent radical selected from the group consisting of ##STR5## where X = CH.sub.2, O, S or ##STR6## (2) an addition type resin intermediate derived from the low molecular weight polyimide monomer ##STR7## wherein R.sub.1 is an unsaturated divalent system such as ##STR8## and (3) an hydroxylated high molecular weight aromatic polyimide in the amic acid stage having the repeating unit ##STR9## wherein n is an integer of sufficient magnitude, e.g., at least approximately 5, to provide a polymer with film forming capability. Suitable examples of polyimide film formers include (1) Upjohn's 2080 polyimide, (2) Rhone-Poulenc's polyimide Nolimide 605, and (3) the polyimide derived from the monomers 5-norbornene-2,3-dicarboxylic acid monomethyl ester, 4,4'-methylenedianiline, and 3,3'-4,4'-benzophenonetetracarboxylic acid dimethyl ester in a molar ratio of 1:1:0.5, respectively.

The other essential ingredient is, by weight, 2-60 percent, preferably 4-40 percent of a silane coupling agent to provide improved adhesion by reacting both with the hydroxylated surface and the resin to provide a substantially permanent bond. Silane coupling agents considered suitable are characterized by the formula

R -- Si -- X.sub.3 wherein R is an organic group containing amino, epoxy, aminehydrochloride or carboxy functionality such as ##STR10## and X is an organic group which contains ether or ester functionality such as --OCH.sub.3, --OCH.sub.2 CH.sub.3, ##STR11## or --OCH.sub.2 CH.sub.2 OCH.sub.3. Suitable coupling agents include (1) .beta.-(3,4-epoxy cyclohexyl) ethyltrimethoxysilane available from Union Carbide as A-186, (2) .gamma.-glycidoxy- propyltrimethoxysilane available from Union Carbide as A-187, .gamma.-N-ureidopropyltriethoxysilane available from Union Carbide as Y-5650, p-carboxyphenylpolysiloxane available from Dow Corning as XZ-8-5041 and .gamma.-aminopropyl- trimethoxysilane hydrochloride available from Dow Corning as XZ-8-5073.

Although not essential, up to approximately 30 percent, by weight, preferably 2-25 percent, of a wetting and lubricating agent may be applied to the hydroxylated surface with the aforementioned film formers and coupling agents. This is particularly so in the case of glass fibers which are to be further processed and which can therefore benefit most from the added lubricity imparted. Suitable wetting/lubricating agents are selected from the group consisting of (1) n-vinylpyrrolidone base polymers having the structure ##STR12## wherein R is H or an alkyl group and n is an integer of sufficient magnitude to give a molecular weight ranging from 7,000 to 20,000, such as those commercially available Ganex polymers V-220, V516 and V-816 and (2) non-ionic silicone compounds having the general formula ##STR13## wherein R is selected from the group consisting of methyl, ethyl, phenyl and hydrogen, X is selected from the group consisting of amine, methoxy or R and n is an integer from 10 to 20. Suitable silicones are amine end blocked dimethyl silicon fluid, amine end blocked diethyl silicon fluid, amine end blocked diphenyl silicon fluid, methoxy end blocked dimethyl silicon fluid, methoxy end blocked diethyl silicon fluid, methoxy end blocked diphenyl silicon fluid, methyl end blocked dimethyl silicon fluid (sold by Union Carbide as L-77), methyl end blocked diethyl silicon fluid and methyl end blocked diphenyl silicon fluid. Union Carbide's non-ionic liquid silicone fluid A-1701 is a suitable wetting/lubricating agent falling within the above definition.

The coating of the present invention, when present at a thickness of approximately 0.02-25 .mu., preferably 0.05-0.20 .mu., acts as a finish to prevent moisture and elevated temperature degradation of glass fibers and to prevent fiber-fiber abrasion. Glass fibers provided with the inventive finish coating find particular utility as reinforcement in the high temperature resins such as epoxy, polyimide, epoxy-polyimide, phenolic, polyquinoxaline, polyphenylquinoxaline and polyimadazoquinazoline and the like. As previously indicated, the finish coating is suitable not only for providing a moisture and heat resistant finish coating for glass fibers such as S-glass or E-glass but for providing such a finish coating for any material with a hydroxylated or oxygen-containing surface such as alumina, carbon or graphite, whether or not in fiber form. By heat resistant is meant the capability of continuous operation at elevated temperatures, as for example, the capability of composites reinforced with fibers having the inventive finish, to withstand temperatures of 550.degree. F while retaining at least 80 percent of their shear strength properties. By moisture resistant is meant the capability of withstanding exposure to humid conditions or boiling water, as for example the capability of glass rovings having the inventive finish to withstand exposure to boiling water vapors for 24 hours and 95 percent relative humidity for 8 weeks at 120.degree. F while retaining at least 80 percent of their tensile strength properties and the capability of composites reinforced with glass rovings having the inventive finish to withstand 24 hours in boiling water or exposure to 95 percent relative humidity for 8 weeks at 120.degree. F while retaining at least 80 percent of their shear strength properties.

BRIEF DESCRIPTION OF THE DRAWINGS

An understanding of the invention will become more apparent to those skilled in the art by reference to the following detailed description when viewed in light of the accompanying drawings wherein:

FIG. 1 is a schematic of apparatus useful in the forming, coating, drying and winding of glass fibers;

FIG. 2 is a graph illustrating 600.degree. F short beam shear strength of composites after 500.degree. F thermal aging;

FIG. 3 is a graph illustrating 600.degree. F flexural strength of composites after 500.degree. F thermal aging; and

FIG. 4 is a graph illustrating 600.degree. F short beam shear strength of composites after 600.degree. F thermal aging.

DESCRIPTION OF THE PREFERRED EMBODIMENT

The inventive coating comprises a polyimide film former, a silane coupling agent and, if desired, a wetting/lubricating agent which, in unique combination, gives a finish coating which prevents fiber-fiber abrasion, bonds to the fiber and the resin matrix and prevents deterioration by moisture as well as by elevated temperatures up to approximately 550.degree. F. The coating may be applied immediately after glass fiber formation or at a subsequent time such as after weaving and heat cleaning.

As described hereinabove, film formers considered useful are those resin materials which form continuous polyimide films over the surface of the glass filament. As indicated, examples of polyimide film formers are Upjohn's 2080 polyimide, Rhone-Poulenc's polyimide Nolimide 605, and the polyimide derived from the monomers 5-norbornene-2,3-dicarboxylic acid monomethyl ester (NE, also called Nadic Anhydride Monomethyl Ester), 4,4'-methylenedianiline (MDA), and 3,3'-4,4'-benxophenonetetracarboxylic acid dimethyl ester (BTDE) in a molar ratio of 1:1:0.5, respectively, all of which polymerize to polyimide films on heating.

Coupling agents useful in the present invention are preferably selected from the group consisting of .beta.-(3,4-epoxy cyclohexyl) ethyltrimethoxysilane (A-186), .gamma.-glycidoxypropyltrimethoxysilane, (Union Carbide's A-187 or Dow Corning's Z-6040), .gamma.-N-ureidopropyltriethoxysilane (Union Carbide's Y-5650), p-carboxyphenylpolysiloxane (Dow Corning's XZ-8-5041) and .gamma.-aminopropyltrimethoxy- silane hydrochloride (Dow Corning's XZ-8-5073). As will be appreciated by those skilled in the art, small amounts of water are added to activate the coupling agent.

While not deemed necessary to the practice of the invention, wetting and lubricating agents are considered useful to impart lubricity to the glass fibers for subsequent handling. Among those agents considered suitable are those commercially available materials such as vinylpyrrolidone polymers called Ganex polymers. Examples are Ganex V-816, V-516 and V-220.

The above components are preferably mixed and placed in solution by the addition of a solvent. Solvents that may be used for those in which all components are soluble such as, for example, N-methylpyrrolidinone (NMP), diacetone alcohol, methanol or a mixture of NMP and xylene.

Referring now to FIG. 1, the procedure used to coat the fibers will be described. As a freshly fiberized glass fiber 10 emerges from conventional bushing 12, it is coated by a continuous stream of coating solution 14 via rotating pulley-type applicator 16. After coating, the fiber passes through a furnace 18 which heats the fiber to a temperature sufficiently high to evaporate the solvent from the coating and, if necessary, to polymerize the resin component. A second coating of coating solution 20, which may or may not be the same as the first coating solution 14, is applied via pulley-type applicator 22. The coated fiber is then passed through a second furnace 24 which evaporates the solvent from the coating and, again if necessary polymerizes the resin component and is wound up onto a take-up reel 26. Located adjacent to each furnace 18 and 24 is an exhaust duct 28 for removing volatiles. As will be appreciated, the fiber is coated tangential to the rotating pulley to minimize abrasion and to encapsulate the fiber completely with the coating solution 14.

In one series of experiments, S-glass was fiberized into monofilaments of approximately 10-12 .mu. diameter and coated immediately as it emerged, at a rate of 55.4 ft/sec. from the bushing. The furnaces utilized were 3-inch diameter by 6-inch long drying furnaces of the clam-shell type heated to 250.degree.-600.degree. C. After coating, monofilaments were wound onto a 12-inch diameter drum over a 1/16 inch width into a 2030 filament roving. In a bushing containing 204 holes, the multifilaments emerged from the bushing and were coated as they converged into a cone-like bundle or strand (end) by means of a conventional guide, then wound onto a 12-inch diameter drum. In these cases, the strand wound packages or cake packs were oven cured at 270.degree. F for 12 hours. The strands were unwound from the cake pack to produce a 10-end or 20-end roving.

The invention is illustrated by the examples that follow.

EXAMPLE 1

In this example, S-glass monofilament was fiberized and treated as above-described. In particular, a polyimide film former available as Upjohn's 2080 polyimide having the formula ##STR14## wherein n is an integer of sufficient magnitude, e.g., at least approximately 5, to provide a polymer with film forming capability, was formulated into a treating composition of:

______________________________________ Wt Wt % referring to (grams) total wt of a, b & c______________________________________a) Polyimide film 2.50 78.1 formerb) Coupling agent 0.50 15.6 (A-186)c) Wetting/lubricating 0.20 6.3 agent (Ganex V-516)d) N-methylpyrrolidinone 86.50 (NMP)______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 2

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 78.1 (Upjohn 2080)b) Coupling agent (A-186) 0.25 15.6c) Wetting/lubricating 0.10 6.3 agent (Ganex V-816)d) NMP 98.4______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 3

S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition, applied both by applicator 16 and applicator 22 consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 0.62 63.9 (Upjohn 2080)b) Coupling agent (A-186) 0.25 25.8c) Wetting/lubricating 0.10 10.3 agent (Ganex V-816)d) NMP 99.00______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 4

S-glass monofilament was fiberized and treated as in Example 1 except that the first treating composition, applied by applicator 16 consisted essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (A-187) 0.25Water 0.07Diacetone alcohol 100.0______________________________________ and the second treating composition, applied by applicator 22 consisted essentially of the treating composition of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 67.6 (Upjohn 2080)b) Coupling agent (A-186 0.50 27.0 + A-187)c) Wetting/lubricating 0.10 5.4 agent (V-816)d) Water 0.07e) NMP 98.4f) Diacetone alcohol 100.0______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 5

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (A-187) 0.50Wetting/lubricating 0.10agent (V-816)Water 0.13Diacetone alcohol 100.0______________________________________ and the second treating composition being that of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 56.8 (Upjohn 2080)b) Coupling agent (A-186 0.75 34.1 + A-187)c) Wetting/lubricating 0.20 9.1 agent (V-816)d) Water 0.13e) NMP 98.4f) Diacetone alcohol 100.0______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 6

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (A-186) 0.25Water 0.07Diacetone alcohol 100.00______________________________________ and the second treating composition being that of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 67.6 (Upjohn 2080)b) Coupling agent (A-186) 0.50 27.0c) Wetting/lubricating 0.10 5.4 agent (Ganex V-816)d) Water 0.07e) NMP 98.4f) Diacetone alcohol 100.00______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 7

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (Y-5650) 0.50Wetting/lubricating 0.10agent (Ganex V-816)Water 0.13______________________________________ and the second treating composition being that of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 56.8 (Upjohn 2080)b) Coupling agent (A-186 0.75 34.1 + Y-5650)c) Wetting/lubricating 0.20 9.1 agent (Ganex V-816)d) Water 0.13e) NMP 98.4______________________________________ A uniform continuous finish coating approximately 0.05-0.29 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 8

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (Y-5650) 0.50Wetting/lubricating 0.50agent (Ganex V-516)Water 0.13______________________________________ and the second treating composition being that of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 48.1 (Upjohn 2080)b) Coupling agent (A-186 0.75 28.8 + Y-5650)c) Wetting/lubricating 0.60 23.1 agent (Ganex V-816 + V-516)d) Water 0.13e) NMP 98.4______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 9

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (A-187) 0.50Wetting/lubricating 0.25agent (L-77)Water 0.14Diacetone alcohol 99.30______________________________________ and the second treating composition being that of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former (Upjohn 2080) 1.25 53.2b) Coupling agent (A-186 0.75 31.9 + A-187)c) Wetting/lubricating 0.35 14.9 agent (V-816 + L-77)d) Water 0.14e) NMP 98.40f) Diacetone alcohol 99.30______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 10

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (A-187) 0.25Wetting/lubricating 0.50agent (A-1701)Water 0.07Diacetone alcohol 100.00______________________________________ and the second treating composition being that of Example 2 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 53.2 (Upjohn 2080)b) Coupling agent (A-186 0.50 21.3 + A-187)c) Wetting/lubricating 0.60 25.5 agent (V-816 + A-1701)d) Water 0.07e) NMP 98.40f) Diacetone alcohol 100.00______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 11

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition consisting essentially of:

______________________________________ Wt (grams)______________________________________Coupling agent (A-187) 0.25Wetting/lubricating 0.10agent (V-516)Water 0.07Diacetone alcohol 99.60______________________________________ and the second treating composition being that of Example 3 for a combined treating composition of: ______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 0.62 46.9 (Upjohn 2080)b) Coupling agent (A-186 0.50 37.9 + A-187)c) Wetting/lubricating 0.20 15.2 agent (V-516 + V-816)d) Water 0.07e) NMP 99.00f) Diacetone alcohol 99.60______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 12

S-glass monofilament was fiberized and treated as in Example 11 except that the second treating composition consisted essentially of that of Example 1. Thus the combined treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 2.50 75.8 (Upjohn 2080)b) Coupling agent (A-186 0.50 15.1 + A-187)c) Wetting/lubricating 0.30 9.1 agent (V-516)d) Water 0.07e) NMP 86.50f) Diacetone alcohol 99.60______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 13

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 2.50 87.7 (Upjohn 2080)b) Coupling agent (A-187) 0.25 8.8c) Wetting/lubricating 0.10 3.5 agent (V-816)d) NMP 97.25______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 14

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.25 78.1 (Upjohn 2080)b) Coupling agent (A-187) 0.25 15.6c) Wetting/lubricating 0.10 6.3 agent (V-816)d) NMP 98.5______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 15

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.00 74.1 (Upjohn 2080)b) Coupling agent (A-187) 0.25 18.5c) Wetting/lubricating 0.10 7.4 agent (V-816)d) NMP 98.75______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 16

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 5.00 93.4 (Upjohn 2080)b) Coupling agent (A-187) 0.25 4.7c) Wetting/lubricating 0.10 1.9 agent (V-816)d) NMP 94.65______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 17

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that the treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.00 57.2 (Upjohn 2080)b) Coupling agent (A-187) 0.50 28.6c) Wetting/lubricating 0.25 14.2 agent (V-516)d) NMP 9-.5______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 18

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition being that of Example 14 and the second treating composition being that of Example 3 for a combined treating composition of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 1.87 72.8 (Upjohn 2080)b) Coupling agent (A-186 0.50 19.4 + A-187)c) Wetting/lubricating 0.20 7.8 agent (V-816)d) NMP 197.5______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 19

S-glass monofilament was fiberized and treated as in Example 4 with the first treating composition being that of Example 3 and a polyimide film former derived from polymerization of monomers on the fiber surface labeled as 100P13, having the formula ##STR15## where R.sub.1 is an unsaturated divalent system such as ##STR16## The combined treating composition consisted essentially of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 3.58 91.2 (100P13 + 2080)b) Coupling agent (A-186) .25 6.3c) Wetting/lubricating 0.10 2.5 agent (V-816)d) NMP 99.00e) Diacetone alcohol 97.0______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

EXAMPLE 20

In this example, S-glass monofilament was fiberized and treated as in Example 1 except that Nolimide 605 from Rhone-Poulenc was used. Nolimide 605 is an hydroxylated aromatic polyimide having the repeating unit ##STR17## wherein n is an integer of sufficient magnitude, e.g., at least approximately 5, to provide a polymer with film forming capability, which was formulated into a treating composition of:

______________________________________ Wt (grams) Wt %______________________________________a) Polyimide film former 5.00 89.3 (Nolimide 605-60 w/o in NMP/methanol-4:1)b) Coupling agent (A-186) 0.50 8.9c) Wetting/lubricating 0.10 1.8 agent (V-816)d) Diacetone alcohol 20.0e) NMP 75.0______________________________________ A uniform continuous finish coating approximately 0.05-0.20 .mu. thick remained on the S-glass after passage through furnaces 18 and 24.

Two types of strength tests were used to evaluate the ability of the inventive coatings to protect the monofilament from the degradative effects of moisture: (1) tensile strength of rovings before and after moisture exposures, and (2) short beam shear strength of unidirectional glass fiber/resin composites before and after moisture. Table I below shows the tensile strength of 2030 filament rovings exposed to boiling water vapors and 95 percent relative humidity (RH) at 120.degree. F for 8 weeks, with comparisons with uncoated fibers and commercial fibers. The superiority of the novel finishes compared to the unfinished glass and commercial glass is readily apparent.

Table I______________________________________TENSILE STRENGTH OF GLASS FIBERSCOATED WITH MOISTURE RESISTANT FINISHES Tensile Strength Dry.sup.1 Wet.sup.2 HC.sup.3Example 10.sup.3 psi 10.sup.3 psi 10.sup.3 psi______________________________________1 257 288 3252 367 385 3343 330 345 3284 315 334 2945 300 311 3456 296 291 3557 408 373 4438 357 343 3679 300 343 30410 367 363 39511 242 241 30612 327 350 367Unfinished S-glass 390 142 254(2030 filament)Ferro 961 S-glass with 340 183 276commercial S-24 finish(multifilament 20 end)" 350 222 216" 193 235Owens-Corning 901 408 288 334S-glass with commercialHTS finish (multifilament12 end)" 410 214 348" 404______________________________________ .sup.1 Dry-tested at room temperature (RT) 2 to 3 weeks after fabrication .sup.2 Wet-tested at RT after 24 hours boiling water vapor exposure. .sup.3 HC-tested at RT after exposure to 95% RH at 120.degree. F for 8 weeks.

Various of the glass filaments described in the examples above were fabricated as reinforcements in resin matrix composites. As the finished glass fiber was wound onto a 12-inch diameter drum over a 11/2 inch width, a 50 weight percent solution of resin in acetone was applied by a brush-type applicator. After approximately 340,000 feet of the fiber was wound up, composites were cut to sizes of either 1 or 11/2 inches wide by 21/4 inches long by approximately 0.10 inch thick.

Table II lists short beam shear strength of laminates made from the coated fibers and the noted epoxy resins.

Table II__________________________________________________________________________SHORT BEAM SHEAR STRENGTH OF UNIDIRECTIONALFIBER GLASS/RESIN COMPOSITESMADE FROM FRESHLYFIBERIZED S-GLASS CONTAINING MOISTURE RESISTANT FINISHES Short BeamComposite from Density Fiber Void Shear Strength, psi.sup.4Ex. No. Resin g/cc Vol % Vol % Dry Wet.sup.6 HC.sup.7__________________________________________________________________________3 ERL 2256/0820.sup.1 2.00 61.4 0 14,450 12,250 12,7603 " 2.01 61.0 0 14,100 11,250 11,4002 " 2.06 60.7 1.95 13,280 10,930 10,05018 ERX-67/MDA.sup.2 2.26 69.8 0 13,225 11,350 12,0153 " 2.15 63.9 6.6 10,385 10,215 9,8601 " 2.14 56.5 1.59 12,600 10,900 9,86219 100P13 2.07 65.7 0.83 14.725 14,365 12,685Commercial Ferro ERX-67/MDA.sup.2 2.18 61.9 1.7 12,000 9,510 10,900S-glass with S-24Finish" ERL 2256/0820.sup.1 1.90 54.0 0.43 12,800 9,740 9,550" " 1.92 53.0 0.0 14,200 11,350 12,100" " 1.88 52.4 0.38 13,300 10.885 10,880Owens-Corning " 1.85 50.0 0.85 12,900 11,200 11,650S-glass with HTSFinish" " 1.96 58.0 0.55 13,385 11,570 11,800__________________________________________________________________________ .sup.1 ERL-2256/ZZl-0820 from Union Carbide Co. is a cycloaliphatic/bisphenol A blend epoxy cured with aromatic amine. .sup.2 ERX-67/MDA from Shell Chemical Co. is a brominated diglycidylaniline (epoxy) cured with 4,4'-methylenedianiline. .sup.3 100P13 is from NE/MDA/BTDE monomers from Aldrich Chemical Co. polymerized on a glass surface to a polyimide in the mol ratio 1:1:0.5. .sup.4 Short beam shear strength, span-to-depth ratio, 5/1. .sup.5 Dry - tested at RT 2 to 3 weeks after fabrication. .sup.6 Wet - tested at RT after 24 hours boiling water exposure. .sup.7 HC - tested at RT after exposure to 95% RH at 120.degree. F for 8 weeks.

In another series of experiments, various composites were made and tested. Composite No. 226 was fabricated according to the following procedure. S-glass monofilament was made and treated with the formulation as described in Example 17 and a 2030 filament roving was produced. The roving was impregnated with 100P13 polyimide resin by immersed passage through 50 weight percent NE/MDA/BTDE monomers in methanol which upon polymerization gives 100P13. After impregnation, the roving was wound onto an 18-inch diameter drum which was lined with MYLAR film to form a prepreg tape 31/2 inches wide. The tape was removed from the drum and cut into pieces by slitting perpendicular to the fiber direction to yield composite tapes 31/2 inches wide by 8 inches long. The tapes were placed on a tray and heated for 30 minutes at 125.degree. C, then for 30 minutes at 190.degree. C. To make a multilayer composite, 18 plies of the tape were stacked in a mold, one over the other, with fiber rovings parallel. The mold was placed in a press, preheated to 300.degree. C and when the temperature inside the mold reached 275.degree. C, a pressure of 1,000 psi was applied, released momentarily and reapplied. The temperature of 300.degree. C and pressure of 1,000 psi were maintained for 1 hour.

Additional composites were made utilizing Owens-Corning S-glass which had been treated with HTS and also Ferro S-glass which has been treated with S-24. Both of these commercially finished glasses were impregnated with 100P13 matrix as above. For the Ferro S-glass composite, an 18-ply composite (No. 225) similar to the one above described was made using the same procedure. For the Owens-Corning S-glass composite, identical procedures and parameters were used except that a 12-ply composite (No. 227) was made.

The finished composites varied in thickness from 90 to 120 mils and were cut into flexural specimens for a four-point test at a span-to-depth ratio of 16/1 and short beam shear specimens for measurement at a span-to-depth ratio of 5/1. These specimens were thermally aged, weight changes determined and then subjected to various mechanical tests described below. The physical properties of the composites are listed in Table III.

Table III______________________________________PHYSICAL PROPERTIES OF UNIDIRECTIONAL100P13 POLYIMIDE COMPOSITES CompositionComposite Fiber Volume Percent DensityNo. Finish Fiber Resin Void g/cc______________________________________225 S-24 73.5 24.5 2.0 2.25227 HTS 73.5 25.0 2.0 2.27226 Ex. 17 66.4 33.2 0.5 2.06______________________________________

The mechanical properties of the composites at room temperature, dry and after exposure to moist environments, are listed in Table IV.

Table IV__________________________________________________________________________ROOM TEMPERATURES SHEAR AND FLEXURAL STRENGTHOF UNIDIRECTIONAL S-GLASS/POLYIMIDE COMPOSITESShort Beam Flexural PropertiesComposite Shear Strength, psi Strength, 10.sup.3 psi Modulus, 10.sup.6 psiNo. Dry.sup.1 Wet.sup.2 HC.sup.3 Dry Wet HC Dry Wet HC__________________________________________________________________________225 7,600 6,180 6,465 52.0.sup.4 90.3.sup.4 74.5.sup.4 9.03 8.7 9.18227 7,100 5,545 8,430 83.7.sup.4 75.9.sup.4 77.3.sup.4 9.95 9.0 9.45226 12,800 5,645 6,675 198.0.sup.4 81.4.sup.4 69.0.sup.4 12.8 8.12 8.75__________________________________________________________________________ .sup.1 Tested within four weeks after composite was fabricated. .sup.2 Tested after exposure to 24-hour water boil. .sup.3 Tested after exposure to 95% RH at 120.degree. F for eight weeks. .sup.4 Shear failure.

As can be seen, the Example 17 finish on the glass rovings of Composite 226 improved the dry shear and flexural strength relative to the other composites.

The elevated temperature (600.degree. F) strength properties of the composites, dry and after exposure to the moist environments, are listed in Table V.

Table V__________________________________________________________________________HIGH TEMPERATURE STRENGTH OF UNIDIRECTIONAL S-GLASS/POLYIMIDE COMPOSITESAFTER ENVIRONMENTAL AGINGShort Beam Flexural Properties, 600.degree. FComposite Shear Strength, 600.degree. F psi Strength, 10.sup.3 psi Modulus, 10.sup.6 psiNo. Dry.sup.1 Wet.sup.2 HC.sup.3 Dry.sup.1 Wet.sup.2 HC.sup.3 Dry.sup.1 Wet.sup.2 HC.sup.3__________________________________________________________________________ 7225 2,690 3,380 2,755 37.5.sup.4 46.4.sup.4 45.8.sup.4 9.10 9.20 9.73227 3,890 4,350 3,645 51.0.sup.4 44.0.sup.4 47.1.sup.4 11.2 11.0 9.9226 7,175 5,300 4,695 88.5.sup.4 64.2.sup.4 62.5.sup.4 9.8 -- 9.4__________________________________________________________________________ .sup.1 Tested within four weeks after composite was fabricated. .sup.2 Tested after exposure to 24-hour water boil. .sup.3 Tested after exposure to 95% RH at 120.degree. F for eight weeks. .sup.4 Shear failure.

As will be noted, Composite 226 exhibits superior shear and flexural strength in the dry condition. In addition, Composite 226 exhibits significantly superior strength retention after 24 hour water boil and 95 percent relative humidity exposures. It is significant that Composite 226 contains less fiber reinforcement than Composites 225 and 227 since this should have led to decreased initial flexural strength rather than increased structural strength. This indicates that load transfer via the interface between resin and fiber reinforcement is more efficient in this composite system than in the composites containing the greater amount of fiber reinforcement.

Composite specimens were exposed to flowing air (100 cc/min) for several hundred hours under isothermal conditions (550.degree. F). Some of the composites were removed after 264 hours, others after 668 hours and the remainder after 1,004 hours.

Referring now to FIGS. 2 and 3, there is illustrated, respectively, 600.degree. F short beam shear strength data after 500.degree. F thermal aging and 600.degree. F flexural strength data after 500.degree. F thermal aging. Further tests were conducted wherein composite shear strength was measured after isothermal aging for 500 and 1,000 hours at 600.degree. F. The results are shown in FIG. 4.

The inventive finish coating is applicable to other materials other than glass, as already discussed and as illustrated in the following example.

EXAMPLE 21

Commercially available Modmor-IIS graphite yarn was heat treated in a pure nitrogen atmosphere at 900.degree. C for 4 seconds and immediately coated with NE/MDA/BTDE monomer solution by immersed passage therethrough and wound onto a take-up drum. The wound yarn was cut into tape 11/2 inches by 4 inches and was heated to 122.degree. F for 2 hours in a mold and then imidized at 400.degree. F for 3 hours. The mold was then inserted into a 600.degree. F preheated press. Contact pressure was applied for 20 minutes until advanced polymerization occurred and then 800 psi was applied. The composite was allowed to reach 600.degree. F and then held at 800 psi and 600.degree. F for 1 hour. The composite was then cooled slowly to room temperature and tested. Room temperature shear strength was as high as 16,900 psi, indicating strong adhesion between the resin and the fiber, initial 600.degree. F interlaminar shear was 9,180 psi and there was no tensile strength degradation of the yarn.

What has been set forth above is intended primarily as exemplary to enable those skilled in the art and the practice of the invention and it should therefore be understood that, within the scope of the appended claims, the invention may be practiced in other ways than as specifically described.

Claims

1. A moisture and heat resistant finish coating on materials having a hydroxylated surface consisting essentially of approximately, by weight, 40-98 percent of a polyimide film former selected from the group consisting of (1) a fully imidized and polymerized polyimide containing the repeating unit ##STR18## wherein R.sub.1 is a tetravalent radical selected from the group consisting of ##STR19## wherein X = O, S, SO.sub.2, CH.sub.2, ##STR20## and R.sub.2 is a divalent aromatic or aliphatic radical selected from the group consisting of ##STR21## and R.sub.3 is an aromatic divalent radical selected from the group consisting of ##STR22## where X = CH.sub.2, O, S or ##STR23## (2) an addition type resin intermediate derived from the low molecular weight polyimide monomer ##STR24## wherein R.sub.1 is an unsaturated divalent system such as ##STR25## and (3) an hydroxylated aromatic polyimide in the amic acid stage having the repeating unit ##STR26## wherein n is an integer of sufficient magnitude, e.g., at least approximately 5, 2-60percent of a silane coupling agent characterized by the formula

R -- Si -- X.sub.3

wherein R is an organic group containing amino, epoxy, aminehydrochloride or carboxy functionality such as ##STR27## and X is an organic group which contains ether or ester functionality such as --OCH.sub.3, --OCH.sub.2 CH.sub.3, ##STR28## or --OCH.sub.2 CH.sub.2 OCH.sub.3 and up to 30 percent of a wetting and lubricating agent, said finish coating having a thickness of approximately 0.02-25 microns.

2. In a composite comprising a resin matrix reinforced with glass fibers embedded therein, the improvement which comprises a mositure and heat resistant finish coating on the surface of said glass fibers bonded to said fibers and said resin consisting essentially of approximately, by weight, 40-98 percent of a polyimide film former selected from the group consisting of (1) a fully imidized and polymerized polyimide containing the repeating unit ##STR29## wherein R.sub.1 is a tetravalent radical selected from the group consisting of ##STR30## wherein X = O, S, SO.sub.2, CH.sub.2, ##STR31## and R.sub.2 is a divalent aromatic or aliphatic radical selected from the group consisting of ##STR32## and R.sub.3 is an aromatic divalent radical selected from the group consisting of ##STR33## where X = CH.sub.2, O, S or ##STR34## (2) an addition type resin intermediate derived from the low molecular weight polyimide monomer ##STR35## wherein R.sub.1 is an unsaturated divalent system such as ##STR36## and (3) an hydroxylated aromatic polyimide in the amic acid stage having the repeating unit ##STR37## wherein n is an integer of sufficient magnitude, e.g., at least approximately 5, 2-60 percent of a silane coupling agent characterized by the formula

R -- Si -- X.sub.3

wherein R is an organic group containing amino, epoxy, aminehydrochloride or carboxy functionality such as ##STR38## and X is an organic group which contains ether or ester functionality such as --OCH.sub.3, --OCH.sub.2 CH.sub.3, ##STR39## or --OCH.sub.2 CH.sub.2 OCH.sub.3 and up to 30 percent of a vinylpyrrolidone polymer wetting and lubricating agent, said coating having a thickness of approximately 0.02-25 microns.

3. The invention of claim 2 wherein said finish coating consists essentially of approximately, by weight, 60-90 percent of said polyimide film former, 10-30 percent of said silane coupling agent and 2-10 percent of said wetting and lubricating agent.

4. The invention of claim 3 wherein said coating has a thickness of 0.02-1.0 microns.

5. The invention of claim 2 wherein said polyimide film former has the formula ##STR40## wherein n is an integer of sufficient magnitude, e.g., at least approximately 5, to provide a polymer with film forming ability.

6. The invention of claim 2 wherein said polyimide film former is derived from polymerization on the fiber surface of monomers having the formula ##STR41## where R.sub.1 is an unsaturated divalent system such as ##STR42##