Partially Alkylated Triamines and Higher Polyamines as Curing Agents in Polyurethane Manufacture by Reaction Injection Molding

As a subclass of commercially available polymers, polyurethane elastomers have several properties whose advantages confer unique benefits on these products. Typically, polyurethanes show high abrasion resistance with high load bearing, excellent cut and tear resistance, high hardness, resistance to ozone degradation, yet are pourable and castable. Compared to metals, polyurethanes are lighter in weight, less noisy in use, show better wear and excellent corrosion resistance while being capable of less expensive fabrication. Compared to other plastics, polyurethanes are non-brittle, much more resistant to abrasion, and exhibit good elastomeric memory. Polyurethanes find use in such diverse products as aircraft hitches, bushings, cams, gaskets, gravure rolls, star wheels, washers, scraper blades, impellers, gears, and drive wheels.

Part of the utility of polyurethanes derives from their enormous diversity of properties resulting from a relatively limited number of reactants. Typically, polyurethanes are prepared on site by curing urethane prepolymers, which are adducts of polyisocyanates and polyhydric alcohols. A large class of such prepolymers are approximately 2:1 adducts of a diisocyanate, OCN--Y--NCO, and a diol, HO--Z--OH, whose resulting structure is OCN--Y--NHCO.sub.2 --Z--O.sub.2 CNH--Y--NCO. Although Y is susceptible of great variety, usually being a divalent alkyl, cyclohexyl, or aromatic radical, in fact the most available prepolymers are made from toluene diisocyanate (TDI), most readily available as a mixture of 2,4-and 2,6-isomers which is rich in the former isomer, or methylene-4,4'-diphenyldiisocyanate (MDI). The diols used display a greater range of variety; Z may be a divalent alkyl radical (i.e., an alkylene group), and the diols frequently are ethers or esters which are the condensation products of glycols with alkylene oxides or dicarboxylic acids, resp.

The polyurethane elastomers are formed by curing the prepolymer. Curing is the reaction of the terminal isocyanate groups of the prepolymer with active hydrogens of a polyfunctional compound so as to form high polymers through chain extension and, in some cases, crosslinking. Diols, especially alkylene diols, are the most common curing agents for MDI-based prepolymers, and representing such diols with the structure HO--X--OH, where X is an organic moiety, most usually an alkylene group, the resulting polymer has as its repeating unit,

Where a triol or a higher polyhydric alcohol is used crosslinking occurs to afford a nonlinear polymer.

Although other polyfunctional chemicals, especially diamines, are theoretically suitable, with but a few exceptions none have achieved commercial importance as a curing agent. The major exception is 4,4'-methylene-di-ortho-chloroaniline, usually referred to as MOCA, a curing agent which is both a chain extender and a crosslinker. TDI-based prepolymers typically are cured with MOCA, and the resulting products account for perhaps most of the polyurethane elastomer market. One reason that polyhydric alcohols generally have gained acceptance as curing agents is that their reaction with urethane prepolymers is sufficiently fast to be convenient, but not so fast as to make it difficult to work with the resulting polymer. In casting polymers it is desirable that the set-up time be reasonably short, yet long enough for the material to be cast into molds. This property is conventionally referred to as pot life. Generally speaking, diamines react with prepolymers, and especially MDI-based prepolymers, so quickly that they are not usable as curing agents. However, primary aromatic diamines with electronegative groups on the aromatic ring, or with alkyl groups ortho to the amino moiety, exhibit sufficiently decreased reactivities with some prepolymers as to afford a desirable pot life, hence the use of, for example, MOCA as a curing agent for TDI-based prepolymers. However, MOCA and others of the aforementioned diamines still remain too reactive to be used, for example, with MDI-based prepolymers.

On the other hand, the advent of reaction injection molding (RIM) provides a means of processing polyurethanes which is well adapted to a short pot life. Reaction injection molding is a process that allows polymerization and crosslinking to take place simultaneous with forming of a part into its final shape. Because of the rapid curing of polyurethanes, compatible with the fast cycle times of RIM, these polymers seem exceptionally well suited to RIM processing although epoxies, nylons, and even polyesters have been made by the RIM process.

In RIM, two highly reactive streams of chemicals are brought together under high pressure in a small mixing chamber where the streams are impingement mixed by being sprayed directly into each other before entering the mold. The mixed material flows directly into a mold at 0.35-0.7 MPa (50-100 psi), a low pressure compared to that used in standard injection molding, where the chemical reaction is completed and the part cures. One of the ingredient streams (the first stream) contains the isocyanate and the other stream (the second stream) contains components having isocyanate-reactive hydrogens, such as polyols and amines, and other components as catalysts, pigments, blowing agents, and surfactants. Much of the technology is currently used in the automotive industry to produce parts such as bumper covers and fenders. Parts are produced on a cycle of 3 minutes or less, and large urethane parts have been successfully demolded in 30 seconds or less after injection.

We have found that a large class of fully or partially alkylated aromatic polyamines, which can be viewed as polymers whose repeating unit is x-amino-y-methylenephenyl, are excellent isocyanate-reactive components, or curing agents, for polyisocyanates in the preparation of RIM elastomers. Among the advantages of the curing agents of this invention are that the resulting elastomers can be expected to show excellent compression set, to have quite high tensile strength, and to show a substantially higher glass transition temperature than usual with good solvent resistance. The resulting elastomers are thermosetting polymers, and also have the advantage that their properties remain relatively unchanged within a wide range of stoichiometry of curing agent and polyisocyanate. Therefore, the curing agents of this invention are very tolerant to mixing error, which is a decided manufacturing advantage. Additionally, the curing agents themselves for the most part are viscous liquids at room temperature, facilitating their use at RIM temperature. The curing agents may be used for both TDI and MDI-based polyisocyanates, which give rise to the two largest classes of polyurethane and polyurea elastomers, and have excellent thermostability. In short, the unique properties of both the curing agents and the resulting elastomers make each very highly desirable in RIM formulations.

To aid in exposition the isocyanate-reactive components can be classified as either polyols (polyhydric alcohols) or polyamines. Each of these classes has two functionally defined subclasses; backbone polyols (or polyamines) and chain extender polyols (or polyamines). The difference is that, e.g., the backbone polyol, being more reactive, reacts with the isocyanates in the first stream to afford short polymeric segments, and the chain extender polyamine links the short segments to form longer chains. The polyamines of this invention act as chain extender polyamines.

The RIM elastomers which can be made from the amines of this invention are diverse and depend upon the nature of the isocyanate-reactive stream. In one variant the second stream as the isocyanate-reactive component is a mixture of backbone and chain extender polyamines. That is, the second stream may have catalysts, pigments, surfactants, etc., but contain little, if any, isocyanate-reactive components other than the polyamines. In this variant the elastomer is exclusively, or almost so, a polyurea.

In another variant the second stream has as the isocyanate-reactive component a mixture of the amines of this invention, which act as chain extender amines, and various backbone polyols. The mixture will generally have from about 20 to about 80% of amine, on an equivalents basis, and more usually contains 30-70 equivalents percent of amine. (An equivalent of polyamine or polyol is an amount which furnishes as many amino or hydroxyl groups as there are isocyanate groups in the first stream. As used herein, "equivalents percent" refers to the percentage of amine and/or polyol equivalents relative to isocyanate equivalents.)

In each of the foregoing variants a portion of the chain-extender polyamines of this invention may be replaced by a chain extender polyol or a second chain extender polyamine. Although this will be described more fully within, to exemplify one of these subvariants the second stream may contain a backbone polyamine, the chain extender polyamines of this invention, and a chain extender polyol where the polyol level is roughly 20-50 equivalents percent of the chain extender polyamine.

The object of this invention is to prepare polyurethane and polyurea elastomers by reaction injection molding using fully or partially alkylated aromatic polyamines as curing agents. In an embodiment the curing agent is an alkylated polymer whose repeating unit is x-amino-y-methylenephenyl, where the alkyl group contains up to about 20 carbon atoms. In a more specific embodiment the polyamine has up to two-thirds of its amino groups alkylated. In a still more specific embodiment the curing agent has from 1-10 repeating units. Other objects and embodiments will become obvious from the description which follows.

In one aspect the invention herein is a reaction injection molded elastomer made by reacting a polyisocyanate and a mixture of isocyanate-reactive material having one or more polyamines of this invention as a chain extender polyamine. Where the mixture is a blend of backbone and chain extender polyamines the resulting elastomers may be viewed as polyureas. Where the mixture is a blend of backbone polyol and chain extender polyamines the resulting elastomers may be viewed as mixed polyureas-polyurethanes. However, it will be understood by those skilled in the art that the elastomers made according to the latter are complex chemical structures having both polyurethane and polyurea segments.

The nature and breadth of our invention may be summarized by characterizing the reactive components in the two streams as well as their ratio of equivalents. The key for the following table is:

I=polyisocyanate;

B.sub.A, B.sub.o =backbone polyamine and polyol, resp.;

P=polyamine of this invention;

E.sub.A, E.sub.o =chain extender polyamine and polyol, resp.

The combination of specified components along with their ratios then fully define this invention. Those ratios which are independent variables, their verbal characterization, and their values for variants of our invention follow.

The ratio r.sub.1, ##EQU1## is the ratio of equivalents of isocyanate-reactive components in the second stream to the polyisocyanate in the first stream. In all cases this ratio is between 0.7 and 1.3, and more generally is between 0.85 and 1.05, and even more frequently is between about 0.90 and about 1.0.

The ratio r.sub.2, ##EQU2## is the ratio of equivalents of the polyamines of this invention plus other chain extenders, if any, to the total isocyanate-reactive components of the second stream. In all cases r.sub.2 is between 0.2 and 0.8, with the preferred ratio being from about 0.3 to about 0.7. Stated differently the ratio varies around a central point where the number of equivalents of the backbone polyamine or polyol is equal to that of the other isocyanate-reactive components of the second stream.

In one variant E.sub.A, E.sub.o =0, i.e., there are no chain extenders in the second stream other than the polyamines of this invention. This corresponds to case 1 and case 3 resp.

In another variant the second stream contains a chain extender polyol in addition to the other isocyanate-reactive components B.sub.A (or B.sub.o) and P. This polyol is present to the extent of about 20 to about 50 equivalents percent based on the polyamines of this invention. Since the polyamines of this invention have been designated as chain extender polyamines, the foregoing is equivalent to the statement that chain extender polyols constitute from about one-sixth to about one-third of the total chain extender mixture. That is, r.sub.3, where ##EQU3## ranges between about 0.17 and about 0.33.

In the last variant to be discussed here the second stream contains a second chain extender amine in addition to the other isocyanate reactive components B.sub.A (or B.sub.o) and P. In this case the polyamines of our invention are only a minor component, with the second chain extender amine constituting 80-99 equivalents percent of the chain extender components. Defining r.sub.4 as, ##EQU4## this ratio of equivalents is between about 0.80 and about 0.99.

A broad variety of polyisocyanates may be used in the preparation of RIM elastomers and may be exemplified by such materials as the toluene diisocyanates, p- and m-phenylene diisocyanate, tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 1,4-cyclohexylene diisocyanate, 4,4'-methylenedicyclohexyl diisocyanate, 4,4'-methylenediphenyl diisocyanate, 3,3'-dimethyl-4,4'-diphenylmethane diisocyanate, 1,5-tetrahydronaphthalene diisocyanate, dianisidine diisocyanate, bitolylene diisocyanate, naphthalene-1,4-diisocyanate, bis(2-methyl-3-isocyanatophenyl)methane, bis(3-methyl-4-isocyanatophenyl)methane, and 4,4'-diphenylpropane diisocyanate.

Also frequently used in RIM processing are methylene-bridged polyphenyl polyisocyanates such as are described and discussed in U.S. Pat. No. 4,433,067, especially the polyisocyanates based on methylenediphenyl diisocyanate, especially the 4,4'-isomer and the uretonimine modified MDI as described therein. The term polyisocyanate also includes quasi prepolymers of polyisocyanates with active hydrogen containing materials where the polyisocyanate is typically reacted with from about 0.05 to about 0.3 equivalents of a polyol. In principle a vast number of polyisocyanates are suitable for making RIM elastomers. However, in practice polyisocyanates based on MDI are currently those principally used in commerce.

If the polyamines of this reaction are used as the sole isocyanate-reactive component of the second stream the resulting elastomer is too brittle to be usable. Consequently, it is necessary to have as another isocyanate-reactive component one which will provide a soft segment in the resulting elastomer. We here refer to such components as backbone polyamines and backbone polyols.

The backbone polyamines used in RIM are well known to those skilled in the art but will be mentioned here, though not in great detail, and include diamines, triamines, and possibly higher polyfunctional amines which are primary amines. One class of such amines is related to aminodiphenylmethane-ethers and esters of the formulae,

In these compounds X is usually an alkylene group, an alkyleneoxy group, or a poly(alkyleneoxy) group. A similar set of backbone polyamines used in RIM results from substitution of both H.sub.2 NC.sub.6 H.sub.4 CH.sub.2 C.sub.6 H.sub.4 NHC(O)-- groups by H.sub.2 NC.sub.6 H.sub.3 (CH.sub.3)NHC(O)-- moieties.

Another class of backbone polyamines have the formula H.sub.2 N--Y--NH.sub.2. In one group Y is an alkylene chain. In a larger group Y is a poly(alkyleneoxy) or a polyester moiety with an alkylene group at both terminii. So, for example, in this group are amine-capped polyols which are the reaction product of a polyol and then an amine with alkylene oxides as well as amine-capped hydroxyl-containing polyesters. Materials of molecular weight in the 200-6000 range are most often utilized.

Tri- and higher polyamines of similar structure to that in the foregoing paragraph also may be utilized. For example, the reaction of pentaerythritol with an alkylene oxide will give a polyether product, one terminus of which has the structural unit ##STR1## This can be amine-capped to give a triamine, and if the hydroxyl group at the other terminus is so capped there will result a tetraamine. Both kinds of products may be used as backbone polyamines.

The backbone polyols used in RIM are equally well known. The polyols used are usually dihydric with trihydric and higher polyhydric polyols used to a lesser degree. Examples of suitable polyols include ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4- and 2,3-butylene glycol, 1,6-hexanediol, 1,8-octanediol, neopentyl glycol, cyclohexane dimethanol, 2-methyl-1,3-propanediol, glycerol, trimethylolpropane, 1,2,6-hexanetriol, 1,2,4-butanetriol, pentaerythritol, mannitol, sorbitol, diethylene glycol, triethylene glycol, tetraethylene glycol, poly(ethylenoxy) glycols, generally dipropylene glycol, poly(propylenoxy) glycols, generally dibutylene glycol, poly(butylenoxy) glycols generally, and the polymeric glycol from caprolactone, commonly known as polycaprolactone.

Other polyhydroxy materials of higher molecular weight are polymerization products of epoxides, such as ethylene oxide, propylene oxide, butylene oxide, styrene oxide, and epichlorohydrin, with materials having reactive hydrogen compounds, such as water and, more particularly, alcohols, including ethylene glycol, 1,3- and 1,2-propylene glycol, trimethylolpropane, etc. Amino alcohols may be made by condensing amino-containing compounds with the foregoing epoxides, using such materials such as ammonia, aniline, and ethylene diamine.

Hydroxyl-containing polyesters, polythioethers, polyacetals, polycarbonates, and polyester amides also may be used instead of or together with the foregoing polyols. Suitable polyesters include the reaction product of polyhydric alcohols and polybasic, preferably dibasic, carboxylic acids. The polyhydric alcohols which are often used include the dihydric alcohols mentioned above. Examples of dicarboxylic acids include succinic acid, adipic acid, suberic acid, azelaic acid, sebacic acid, glutaric acid, phthalic acid, maleic acid, and fumaric acid. Hydroxyl-containing polythioethers, polyacetals, polycarbonates, and polyesteramides are less frequently employed in the preparation of RIM elastomers. However, these are sufficiently well known to those practicing the art that they need not be further elaborated upon here.

The elastomer is made by reacting the polyisocyanate with a backbone polyamine or polyol and a fully or partially alkylated aromatic polyamine of the structure, ##STR2## where n is an integer from 1 to about 10, and R.sub.1, R.sub.2, and R.sub.3 are either hydrogen, an alkyl, or an alkenyl group. These polyamines may be viewed as low polymers with the repeating structural unit of x-amino-y-methylenephenyl, where y is 3 or 4, and where x=2, 4, 5, or 6 when y=3, and x=2 or 3 when y=4.

Where one or more of R are alkyl or alkenyl moieties--i.e., a monovalent radical whose parent is a linear or branched alkane or alkene--each is independently selected from the group consisting of alkyl or alkenyl moieties containing from 1 up to about 20 carbon atoms, and more preferably between 1 and about 10 carbon atoms. The alkyl or alkenyl group may be a primary, secondary, or tertiary group, although when it is tertiary there is the risk that cure time may be too long to be commercially acceptable. Secondary alkyl or alkenyl groups are preferred, and among these the secondary butyl group is particularly preferred. Examples of alkyl groups which may be used in the practice of this invention include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, and eicosyl moieties. Examples of alkenyl groups are the unsaturated counterparts of the aforementioned alkyl groups. As stated previously, secondary alkyl or alkenyl groups, i.e., those branched at the carbon atom bound to the nitrogen atom, and secondary alkyl groups in particular, are preferred in the practice of this invention. Representative of such groups are 2-propyl, 2-butyl, 2-pentyl, 3-pentyl, 2-hexyl, 3-hexyl, and so forth.

By "partially alkylated" is meant that the number-average of alkyl groups of the polyamine curing agents of this invention is less than (n+2). In the context of the prior description, this means that on the average something under 100% of the R groups are different from hydrogen. Stated differently, as an example the term "67% alkylated" means that on the average 67%, or two-thirds, of the amino groups in the polyamine are alkylated, i.e., have an alkyl or alkenyl group attached thereto. The degree of alkylation has a profound effect on curing time, and since the latter is an important, sometimes determinative characteristic for RIM elastomers it is the index most often used to establish the extent of alkylation. Cure time will depend not only on the average number of alkyl groups per molecule of polyamine, but also will depend on the nature of such groups, their distribution among the various amino groups in the molecule, the presence of other components if a blend of chain extending agents is used, and the nature of other chain extenders in such a blend. For example, in general it will be found that cure times as a function of R increase in the order, R=H<primary alkyl<secondary alkyl<tertiary alkyl. Therefore, all other things being equal a polyamine with only primary alkyls may be more highly alkylated than one with only secondary or tertiary alkyl groups and still exhibit comparable cure times.

The position of the alkyl group also affects curing time in that the amino group on the terminal benzene ring is more reactive than amino groups of internal rings. Thus, if one or both of the terminal amino groups are preferentially alkylated the resulting amine will have a longer cure time than if the internal amino groups are comparably alkylated. Finally, if a partially alkylated polyamine of this invention is used in a blend with, e.g., chain extender polyols the cure time may be expected to be less sensitive to the degree of alkylation, nature of the alkyls, and their distribution among the various amino groups in the molecule.

In view of the foregoing it should be clear that the alkylated polyamines of this invention can be expected to manifest an enormous range of cure time in RIM. This variability presents distinct advantages in permitting the end user to tailor the polyamine to his particular needs. Since the properties of the resulting elastomer also will vary with the polyamines of this invention, and since many partially alkylated polyamines may be chosen with the same cure time, the end user generally also will have a broad choice of our polyamines depending on the performance characteristics sought for the final product.

The polyamines of this invention may be as little as about 5% alkylated and may be as great as 100% alkylated. Where the polyamines are greater than about 67% alkylated cure times may be too long to be acceptable in RIM. However, since catalysts which increase reaction rate up to 4-5 orders of magnitude are known even such highly alkylated polyamines may be used as a component in RIM manufacture with suitable catalysts in their formulation. The polyamines generally will be at least 5% alkylated, more often at least 10% alkylated, and the range of alkylation between about 33% and about 67% may be the one most often practiced.

The alkylated polyamines of this invention typically are prepared by conventional alkylation procedures performed on the precursor primary amine. Largely because of steric factors the terminal amino groups often are preferentially alkylated. Most usually the extent of alkylation will be determined by the relative molar proportions of alkylating agent and polyamine.

As previously stated n is an integer from 1 to about 10, but for ease of preparation and availability polyamines where n is 1 or 2 are materials of choice. Whatever the value of n, the terminal amino groups may be at either the 2, 3, or 4 position in the polyamine. However, it is desirable that at least 1 of the terminal amino groups be at the 4 position, and even more desirable that both occupy the 4-position. A major advantage arises from the ease of synthesis of such materials, although it is not to be implied that there are no differences in such materials as curing agents. Analogously, polyamines where y is 3 are preferred because of their relative availability.

In the preparation of the alkylated polyamines of this invention the reaction mixture almost invariably contains significant amounts of the di(aminophenyl)methane which is largely dialkylated, i.e., amines of the general formula above where n=0 and R.sub.1, R.sub.3 each is an alkyl or alkenyl group. The average functionality, <f>, of an alkylated polyamine mixture is the average number of amino groups per molecule and may be defined as,

where m.sub.i =moles fraction of component i, and a.sub.i =number of amino groups in component i where a.sub.i =n+2. Mixtures of alkylated polyamines with a functionality as low as 2.3 may be used in the practice of this invention, although normally the average functionality will be above 2.5.

It follows from the definition above that,

What this says is that the average value of n in any polyamine mixture is the average functionality minus two. For example, a polyamine mixture of average functionality 2.7 results from a mixture of 0.3 mole fraction diamine and 0.7 mole fraction triamine. However, it also results from a mixture of 0.4 mole fraction diamine, 0.5 mole fraction triamine, and 0.1 mole fraction tetramine and many, many other combinations. What must be emphasized here is that where reference is made to the "polyamines of this invention" or to a "chain extender polyamine" or to "P" such reference incorporates mixtures containing the aforedescribed diamines where the average functionality of the mixture may be as low as 2.3, but more often is greater than 2.5.

Defining an equivalent of polyamine or polyol as an amount which furnishes as many amino groups or hydroxyl groups, resp., as there are isocyanate groups in the first polyisocyanate stream, from about 0.70 to about 1.3 equivalents total of the backbone polyamine or backbone polyol and our polyamine are used in curing, with the range from about 0.85 to about 1.05 more frequently used, and from about 0.90 to about 1.0 being the more usual one. Since each molecule of our polyamine has at least 3 amino groups, none of which are tertiary, the polyamines of this invention may act both as chain extenders and as crosslinkers. As elaborated upon below the curing mix may contain other materials, including other isocyanate-reactive components such as chain extender polyols and polyamines, in addition to, or partly replacing, the polyamines of this invention, although the presence of such materials may not be necessary to the success of this invention.

As stated above, catalysts may need to be used to decrease the reaction time in order to obtain a mixture which sets sufficiently rapidly in the mold to conform to the process requirements of RIM. Organic tin compounds are probably most frequently used and include such materials as the tin(II) salts of carboxylic acids such as tin(II) acetate, tin(II) octoate, tin(II) ethylhexoate and tin(II) laurate, as well as such materials as the dialkyl tin salts of carboxylic acids as exemplified by dibutyltindiacetate, dibutyltindilaurate, dibutyltinmaleate, and dioctyltindiacetate. Such tin salts may be used either alone or as a complex with amidines such as amino pyridines, amino pyrimidines, hydrazino pyridines, and tetrahydropyrimidines.

Catalysts based on metals such as lead, iron, mercury, cobalt and manganese also have been used, and include compounds such as cobalt (III) acetylacetonate, cobalt naphthoate, manganese naphthoate, lead oleate, zinc naphthenate and zirconium naphthenate. Other catalysts which may be used include tertiary amines such as triethylamine, tributylamine, N-methylmorpholine, 1,4-diaza-bicyclo-(2,2,2)-octane, N-methyl-N'-dimethylaminoethylpiperazine, N,N-dimethylbenzylamine, N,N-dimethylcyclohexylamine, and 1,2-dimethylimidazole.

Other catalysts such as silaamines and basic nitrogen compounds such as tetraalkyl ammonium hydroxide, alkali metal hydroxides such as sodium hydroxide, and alkali metal alcoholates such as sodium methylate also have been used as catalysts. These catalysts are generally used in an amount from about 0.01 to about 10% by weight, preferably from about 0.05 to about 1.0% by weight, based on the quantity of polyisocyanate and the quantity of materials reacting with the polyisocyanate.

The second stream also may contain materials such as blowing agents and surfactants. Among suitable blowing agents are water and readily volatile organic substances or dissolved inert gases such as acetone, ethylacetate, methanol, ethanol, halogen substituted alkanes including methylene chloride, chloroform, vinylidene chloride, monofluorotrichloromethane, chlorodifluoromethane, and dichlorofluoromethane, butane, hexane, heptane, diethyl ether, nitrogen, air, carbon dioxide, etc. Examples of surfactants include the sodium salts of sulfonates or of fatty acids, amine salts of fatty acids, alkali metal or ammonium salts of sulfonic acids, polyether siloxanes, and the like. The second component also may contain pigments, dyes, flame retardants, stabilizers, plasticizers, fungicides and bactericides, and fillers.

As previously noted the blend of backbone polyamine or polyol and the chain extender amines of our invention may also contain one or more chain extender polyols or a second chain extender polyamine. The chain extender polyols used in this branch of our invention are polyhydric alcohols with more than two reactive hydroxyl groups per molecule, i.e., more than two hydroxyl groups per molecule must react with the terminal isocyanate groups of the polyisocyanate. Normally this means the polyols are at least trihydric, but since some trihydric alcohols may have one or more hydroxyl groups unreactive under the reaction conditions of curing, it is not invariably true that a trihydric alcohol will suffice. In particular, phenolic hydroxyl moieties, and hydroxyl groups attached to a tertiary carbon atom, usually will be unreactive in curing polyisocyanates, whereas the hydroxyl moiety associated with primary and secondary alcohols will be reactive. With the use of polyols having more than two reactive hydroxyls per molecule it is clear that such materials act as both cross-linkers and chain extenders, although for convenience we refer to such materials as chain extender polyols. Among the polyols which may be used are included 1,1,1-tri(hydroxymethyl)propane, otherwise known as 2,2-di(hydroxymethyl)-1-butanol, 1,1,1-tri(hydroxymethyl)ethane, N,N,N',N'-tetrakis(2-hydroxypropyl)ethylene diamine, 2,4,6-tris(N-methyl-N-hydroxymethylaminomethyl)phenol, 1,2,6-hexanetriol, 1,2,4-butanetriol, pentaerythritol, mannitol, sorbitol, triglycols, castor oils, triisopropanolamine, and N,N,N',N'-tetrakis(hydroxyethyl)ethylene diamine. Chain extender polyols commonly are used at a level between about 20 and about 50 equivalents percent based on the polyamines of our invention subject to the constraints on the ratios r.sub.1 and r.sub.2 ; vide supra.

Where the blend of backbone polyamine or polyol and the polyamines of our invention contains a second chain extender polyamine, the latter generally is a diamine where both amino groups are primary amino groups, and even more frequently is an aromatic primary diamine. Such materials include 1-methyl-3,5-diethyl-2,4-diaminobenzene, 1-methyl-3,5-diethyl-2,6-diaminobenzene, toluene diamine, 1,3,5-triethyl-2,6-diaminobenzene, 3,3'-dichloro-4,4-diaminodiphenylmethane (MOCA) and the like. When used in a blend with the polyamines of this invention the second chain extender polyamine constitutes the major portion of the blend, viz., from about 80 to about 99 equivalents percent of the mixture of the polyamines of this invention and the second chain extender polyamine is the latter.

The process of reaction injection moldings has been described above and will not be repeated here. Solidification of the reaction mixture after injection into the mold usually takes place so rapidly that the mold may be opened within about 15-30 seconds to afford material with sufficient green strength to be handled. Post curing of the elastomer is optional and will depend on the desired properties of the end product, the various components used, etc. Where post curing is desired it generally will be performed in a range between about 100.degree. C. and about 150.degree. C. for a time between about 1 and about 24 hours.

Typical Rim Formulation. A typical RIM machine for polyurethane and polyurea RIM may be employed without modification. In the A-side (or the isocyanate) reservoir of the RIM machine is added the isocyanate to be used: In this case, a low molecular weight MDI-ether prepolymer. In the B-side reservoir are added the polyol, the polyamines of this invention, and any other co-cures or additives compatible with the polyol and polyamine. In polyurea RIM, the polyol would be replaced with a polyamine in order to form the backbone of the polyurea with the isocyanate. Both the A- and B-sides are cycled through their respective heat exchangers where both are brought up to 70.degree. C. Both sides are flowed to their respective metering pumps which are loaded for the shot. The ratio of the two (which determines the stoichiometry of the final polymer) and the shot size have been predetermined. The pistons of the metering pumps are engaged and the shot forced into the mixing head and through to the mold which is attached to the mixing head and is heated to between 70.degree. and 100.degree. C. After about 30 to 60 seconds, the mold is opened, the part ejected, the mold and the mixing head cleaned, and a new shot readied. The part be post-cured from 30 minutes to 17 hours depending on the type of polymer made and the components used. Several representative formulations and RIM conditions are summarized below.