CA2482741A1 - Polyetherurethaneurea elastomers and thin-walled articles prepared therefrom - Google Patents

Abstract

The present invention provides polyetherurethaneurea (PEUU) elastomers having an excellent combination of elastic properties including low modulus, high elongation, high tensile strength and a high degree of retained stress. Thin-walled films made from these elastomers may be fashioned into items such as medical gloves, scientific gloves, condoms, etc.

Description

Mo-6576 POLYETHERURETHANEUREA ELASTOMERS AND
THIN WALLED ARTICLES PREPARED THEREFROM
FIELD OF THE INVENTION
The present invention relates in general to elastomers, and more specifically, to a polyetherurethaneurea (PEUU) elastomer and to thin-walled elastic articles prepared therefrom. The polyetherurethaneurea (PEUU) elastomer of the present invention exhibits a high degree of retained stress and the thin walled films made therefrom may provide items such as medical gloves, scientific gloves and condoms.
BACKGROUND OF THE INVENTION
Natural rubber latex (NRL) is the material of choice in many applications requiring soft, thin-walled elastic articles, such as medical gloves, scientifc gloves and condoms. NRL articles typically are made by dipping a mandrel, pre-coated with a coagulant, into an aqueous rubber emulsion. To produce NRL gloves which are adequately strong, but which do not have pinholes, the dipped NRL gloves must be about 0.18 to about 0.20 mm thick. Although gloves made from NRL possess an excellent combination of flexibility, high elongation at break, tensile strength and a low degree of creep, in recent years the use of NRL has come under attack due to increased instances of allergic reactions. These allergic reactions are thought to be caused by proteins and vulcanization accelerator residues present in NRL.
Generally a high level of retained stress (> 80°/~) is desired in applications such as surgical gloves so that the article holds its shape and conforms to the fingers throughout prolonged usage. NRL exhibits very low stress relaxation characteristics (typically > 90°~ retained stress). In contrast, virtually all synthetic materials such as nitrite rubber, polyvinylchloride (PVC), etc. exhibit poor retained stress characteristics.
Nitrite rubber is the most widely used synthetic rubber for examination and fVlo-6576 - 2 -clean room gloves (not for surgical gloves). However, its modulus is relatively high and its retained stress characteristics are greatly inferior to those of NRL.
In the past, natural rubber thread was the only material available to provide elasticity to fabrics. Polyurethaneurea eiastomers in the form of fibers and films have found wide acceptance in the textile industry. Those elastomers, called "spandex" ('°~lastane°° is used in Furope), are long chain synthetic polymers containing at least 85% by weight of segmented polyurethane. Spandex, originally developed in the 1950x, has numerous advantages over rubber filaments. The most important of these is its higher modulus. Typically, for a given denier, spandex has at least twice the recovery, or retractive power, of rubber. This allows the manufacture of stretch garments containing less elastic fiber and lighter in weight.
Additional advantages over natural rubber include the ability to produce spandex having much finer deniers, higher tensile strength and abrasion resistance, and in many cases, higher resilience.
Additionally, spandex exhibits improved resistance to many cosmetic oils, to solvents, such as those used in dry cleaning, and a high resistance to oxidation and ozone. Furthermore, unlike rubber filaments, spandex fibers can be dyed relatively easily with certain classes of dye-stuffs.
However, two areas where spandex fibers are inferior to rubber filaments are elongation and mechanical dynamic properties. Spandex fibers typically break at elongations of 500% whereas rubber filaments have elongations at break of 500 to 700%. in addition, rubber exhibits much lower hysteresis than spandex fibers. Hysteresis is a measure of the energy loss during stretching and retraction of an elastic material. A
large energy loss implies heat generation, which can lead to discomfort in wear.
The preparation of polyurethanelurea elastomers by the polyaddition process from high molecular weight, substantially linear polyhydroxy compounds, polyisocyanates and chain lengthening agents Mo-6576 - 3 -that have reactive hydrogen atoms by reaction in highly polar organic solvents is known in the art. The fiormation of fibers, filaments, threads, and films from these solvent-borne polyurethane elastomers is also known. Reference in this regard may be made to U.S. Pat. Nos.
3,483,167 and 3,384,623, which illustrate the preparation of spandex fibers from isocyanate-terminated polymeric diols.
In commercial practice, the preferred polymeric diol for spandex production is poiytetramethylene ether glycol (PTMEG). However, PTMEG-derived prepolymers have high viscosities, and solution viscosities of chain-extended elastomers prepared therefrom are also very high. As a result, the solids content of spandex spinning solutions must generally be kept low, and removal of solvent from the polymer solution becomes the rate-limiting step in spandex fiber production.
It has been known for some time that, in principle, polyoxypropylene glycol could also be used to prepare spandex fibers. U.S. Pat.
No. 3,180,854, for example, discloses a polyurethanelurea fiber based on a 2;000 Da molecular weight polyoxypropylene glycol. However, spandex based on polyoxypropylene glycols of 2,000 Da molecular weight or lower has inferior percent sets. Higher molecular weight polyoxypropylene glycols made by conventional processes contain high percentages of terminal unsaturation or monofunctional hydroxyl-containing species ~eemonOl~~). The mono) is theorized to act as a chain terminator, limiting the formation of the required high molecular weight polymer during the chain extension reaction and thus yielding products generally inferior in comparison to PTMEG derived elastomers. However, the role of monol as a chain terminator may be over-simplified, as severaB patents, e.g. U.S.
Pat. Nos. 3,384,623 and 4,098,772, disclose preparation of elastomers with enhanced physical properties by purposeful addition of monol to polyurethane elastomer fiormulations.
The properties of polyoxypropylene-derived spandex are generally inferior to those based on PTMEG, and therefore, polyoxypropylene glycols have not been utilized commercially in spandex production. (See, Mo-6576 - 4 -e.g., the POLYURETHANE HANDBOOK {Gunther Oertei, Ed., Carl Hanser Verlag Pub., Munich 1985, p. 578: '°Polypropylene glycols have so far been used as soft segments only in experimental products since they produce inferior elastanes°'.) The majority of polyoxyalkylene polyether poiyols are polymerized through base catalysis. For example, polyoxypropylene diols are prepared by the base-catalyzed oxypropylation of a difunctionai initiator such as propylene glycol. During base-catalyzed oxypropylation, a competing rearrangement of propylene oxide to allyl alcohol continually introduces an unsaturated, monofunctional, oxyalkylatable species into the reactor. The oxyalkylation of this monofunctional species yields allyl-terminated polyoxypropylene monols. The rearrangement is .discussed in BLOCK
AND GRAFT POLYMERIZATION, Vol. 2, Ceresa, Ed., John Wiley & Sons, pp. 17-21. Unsaturation is measured in accordance with ASTM D-2849-69 "Testing Urethane Foam Polyol Raw Materials," and expressed as milliequivalents of unsaturation per gram of polyol {meq/g).
Due to this continual creation of allyl alcoho9 and its subsequent oxypropylation, the average functionality of the polyol mixture decreases and the molecular weight distribution broadens. Base-catalyzed polyoxyalkylene polyols contain considerable quantities of lower molecular weight, monofunctionai species. fn polyoxypropylene diols of 4,000 Da molecular weight, the content of monofunctional species may be between and 40 mole %. In such cases, the average functionality is lowered to about 1.6 to 1.7 from the nominal, or theoretical functionality of 2Ø In 25 addition, base-catalyzed polyols have a high polydispersity, MW /Mr, due to the presence of the substantial, low molecular weight fractions.
Lowering unsaturation and the attendant high mono) fraction in polyoxypropylene polyols has been touted as a means of providing polyurethane elastomers with improved properties. Often, formulations 30 must be chosen to balance conflicting properties. For example, increases in tensile strength are often accompanied by a decrease in elongation.

Mo-6576 - 5 -In the early 1960's, double metal cyanide catalysts such as zinc hexacyanocobaltate complexes were developed to lower polyol unsaturation. Such complexes are disclosed in U.S. Patents 3,427,256;
3,427,334; 3,427,335; 3,829,505; and 3,941,849. Although the unsaturation level was lowered to approximately 0.018 meqlg, the cost of these catalysts coupled with the need for lengthy and expensive catalyst removal steps prevented commercialization of processes for the production polyoxyalkylene poiyols using these catalysts.
Other alternatives to basic catalysts such as cesium hydroxide and rubidium hydroxide are disclosed in U.S. Patent 3,393,243. Barium and strontium oxide and hydroxide catalysts (disclosed in U.S. Patents 5,010,187 and 5,114,619) enabled modest improvements with respect to unsaturation levels. However, catalyst expense, and in some cases, toxicity, and the modest level of improvement attributable to these catalysts, mitigated against their commercialization. Catalysts such as calcium naphthenate and combinations of calcium naphthenate with tertiary amines have proven to be useful in preparing polyols with unsaturation levels as low as 0.016 meqlg, and more generally in the range of from 0.02 to 0.04 meqlg. (See, e.g., U.S. Patents 4,282,387;
4,687,851; and 5,010,117.) In the 1980's, use of double metal cyanide complex (DMC) catalysts was revisited. Improvements in catalytic activity and catalyst removal methods encouraged commercial use of DMC catalyzed polyols having low unsaturation levels (in the range of from 0.015 to 0.018 meq/g) for a brief time. However, base catalysis continued to be the primary method used to produce polyoxypropylene polyols. Basic pH catalysts continue to be the catalysts that are primarily used in commercial polyoxyalkylene polyol production processes.
Recent advances in DMC catalysts and polyoxyalkylation processes have enabled the practical preparation of ultra-low unsaturation polyoxypropylene polyols. High molecular weight polyols, for example those in the 4,000 Da to 8,000 Da molecular weight range, typically exhibit Mo-6576 - 6 -unsaturation in the range of 0.004 to 0.007 meq/g if catalyzed by these DMC catalysts. At those levels of unsaturation, the amount of monofunctional species is only 2 mole % or less. Moreover, gel permeation chromatography {GPC) analysis shows those polyols to be virtually monodisperse, often exhibiting polydispersities less than 1.10. A
number of such polyols are commercialized, by the assignee of the present invention, as ACCLAIM polyols. These ultra-!ow unsaturation polyols have been found to be quantitatively different than both conventional polyols and low unsaturation polyols.
Smith et al., in U.S. Pat. No. 5,340,902, disclose spandex fibers prepared from polyoxypropyler9e diols having low unsaturation, less than 0.03 meqlg. Use of low unsaturation polyoxypropylene diofs is stated therein to allow preparation of fibers with properties superior to PTMEG
derived spandex fibers. However, all the examples of Smith et al. appear to be prophetic, and no physical properties are disclosed.
In the substantially contemporaneous publication co-authored by Smith: A.T. Chen et al., '°Comparison of the Dynamic Properties of Polyurethane Elastomers Based on Low Unsaturation Polyoxypropylene Glycols and Poly(tetramethylene oxide) Glycols," POLYURETHANES
WORLD CONGRESS 1993, Oct. 10-13, 1993, pp. 388-399, conventional, base-catalyzed polyoxypropylene diols having normal (high) levels of unsaturation produced polyurethanelurea cast efastomers with physical properties virtually indistinguishable from those prepared from low unsaturation diols, as demonstrated by an actual comparison of physical properties of PTMEG-derived elastomers with those from conventional polyoxypropylene diols and low unsaturation polyoxypropylene diols. In Shore A 90 cast elastomers, PTMEG-MDI prepolymer-derived, butanediol-extended polyurethane elastomers had slightly lower modulus and elongation than low unsaturation polyoxypropylene diol-derived elastomers, however tensile strength of the PTMEG elastomers was considerably higher. For pofyurethanelurea cast elastomers, a direct comparison was not possible, as the only PTMEG example used a 1,000 Mo-6576 - 7 -Da PTMEG whereas both low unsaturation polyoxypropylene diol examples employed approximately 2,000 Da molecular weight diols. The PTMEG example had considerably higher physical properties with the exception of elongation, which was lower as expected due to the lower soft segment molecular weight. However, these results must be viewed with caution, as cast and one shot elastomers cannot be directly compared with spandex elastomers.
GB 2316948 A, in the name of Aisaffar, teaches that polyurethanes made with aromatic isocyanates exhibit unacceptably high modulus (too stiff) and low retained stress (too much creep). As those skilled in the art are aware, films and articles made with aromatic isocyanates tend to yellow excessively. Therefore, Aisaffar prefers to use aliphatic isocyanates. Aliphatic isocyanates are much more expensive than aromatics and thus make it more difficult to compete against natural rubber latex, which is quite inexpensive. Although Alsaffar uses low mono) polyols, there is no mention of using such polyols in combination with a low molecular weight glycol. Alsaffar also prefers 1,4-butanediol as the chain extender.
Dreibelbis, et al. in U.S. Pat. Nos. 5,391,343 and 5,728,340, disclose polyether-based or polyester-based polyurethaneureas in solutions of organic solvent at a 12 to 20% concentration. These polyurethanes are said to be particularly suited for use in a mandrel-dipping process for producing thin-walled elastic articles, such as surgical gloves, which are more resistant to puncture and tear than conventional surgical gloves made from rubber latex. The '343 patent also discloses using polyethers, but specifically those based on THF or from a mixture of THF and 3-methyltetrahydrofuran. The polyether polyols employed by Dreibelbis, et al. are expensive.
U.S. Pat. No. 5,708,118, issued to Seneker, et al. teaches spandex-type segmented polyurethanelurea eiastomers having exceptional elongation, hysteresis, recovery, and other physical properties which are prepared by the amine chain extension of an isocyanate-terminated Mo-6576 - 8 -prepolymer prepared by the reaction of a stoichiometric excess of isocyanate with a polyol blend comprising a low molecular weight diol having a molecular weight below 750 Da with a high molecular weight glycol which may be a 1,500 Da to 20,000 Da molecular weight, ultra-low unsaturation polyoxypropylene glycoP with an unsaturation of less than about 0.010 meqlg.
Snow, et al., in U.S. Pat. No. 6,017,997, disclose a waterborne dispersion of a polyurethane polymer which is said to be useful as a flm having improved mechanical properties. More particularly, the film is said to have properties comparable to rubber; including, a percentage elongation greater than 700°/~; a tensile strength greater than 3,500 psi; a 100% modules below 450 psi; a 300% modules below 700 psi; and, a 500% modules below 1,500 psi. The film of Snow et al. can be prepared in the absence of a solvent, thus making it attractive for a variety of protection products for medical and industrial applications such as gloves, condoms, catheters, and the like. The polymer is said to be useful as coatings for textiles, such as backcoatings, fabric or fiber saturants, finishes, or transfer coatings, or other textile and non-textile applications where good elastomeric properties would be useful. Snow et al. make no mention of blending a high molecular weight low monol PPG polyol with a low molecular weight glycol. Also, the invention of Snow et al. has 100%
modules values of less than 450 psi (or 3.1 mPa) and elongations of greater than 700%.
A need exists, therefore, in the art for an elastomer that will provide the desired properties of natural rubber latex (NRL) including low modules, high elongation, high tensile strength and a high degree of retained stress without the drawbacks associated with NRL, such as allergic reactions.
SUMMARY OF THE INVENTI~N
Accordingly, the present invention provides polyetherurethaneurea (PEUU) elastomers made in an aprotic solvent such as dimethylacetamide (DMAc) which have film properties comparable, or superior, to natural Mo-6576 _ g rubber latex (NRL). A key feature of the polyetherurethaneurea (PEUU) elastomers of the present invention is the low degree of stress relaxation i.e. the elastomers exhibit a high degree of retained stress.
These and other advantages and benefits of the present invention will become apparent from the Detailed Description of the Invention herein below.
DETAILED DESCRIPTION OF THE IN~IENT(ON
The present invention will now be described for purposes of illustration and not limitation. Except in the operating examples, or where otherwise indicated, all numbers expressing quantities, percentages, functionalities and so forth in the specification are to be understood as being modified in all instances by the term "about."
The term "NCO content" herein refers to the isocyanate group content of the prepolymer, before chain extension. The term "molecular weight" means number average molecular weight unless indicated otherwise. The number average molecular weights for the po(yether glycols are each determined from the hydroxyl number of the polyether glycol as measured by the imidazole-pyridine catalyst method described by S. L. Wellon et al., '°Determination of Hydroxyl Content of Polyurethane Poiyols and Other Alcohois°', ANALYTICAL CHEMISTRY, Vol. 52, No.
8, pp. 1374-1376 (July 1980). The molecular weights and equivalent weights given herein in Da (Daltons) are number average molecular weights and number average equivalent weights, respectively, unless specified otherwise.
The present invention provides pofyetherurethaneurea (PEUU) elastomers having an excellent combination of elastic properties including low modulus (for ease of donning & movement by the wearer of articles made therefrom), high elongation, high tensile strength and a high degree of retained stress. The polyetherurethaneurea (PEUU) elastomers of the present invention cannot be made with conventional base-catalyzed PPG
polyols due to those polyois containing high levels of monohydroxy impurities ("monol") leading to low strength and low elongation. The thin Mo-6576 -10 walled film made from these elastomers may find use in items including, but not limited to, medical gloves, scientific gloves and condoms. As the comparative examples in the present disclosure show, this combination of mechanical properties is difficult to achieve using polytetramethylene ether glycol (PTMEG) polyols, which tend to yield very high modules flms.
Although the modules can be lowered by reducing the IVCO:OH ratio of the prepolymer, in PTMEG-based systems this occurs at the expense of an unacceptably high prepolymer viscosity. The 5d0% modules of PTMEG-based films is usually quite high due to the tendency of PTMEG to strain crystallize.
The polyetherurethaneurea (PEUU) elastomers of the present invention may be prepared by a prepolymer process. In such processes, a polyol component, herein called the isocyanate-reactive component, is reacted with an excess of diisocyanate, to yield an isocyanate-terminated prepolymer having a relatively low free isocyanate group content.
Isocyanate contents are preferably from 1 to 2% and more preferably from 1.2 to 2%. The prepolymers may be chain extended in solution to form the final elastorner, which may be made into a film by methods known in the art, although the elastomers may be spun into fiber or extruded or cast into sheets, etc.
As those skilled in the art are aware, spandex-type elastomers prepared by the chain extension of an isocyanate-terminated prepolymer in aprotic solvent cannot be compared with those elastomers prepared by one-shot or quasi-prepolymer processes, as both of the latter introduce a significant amount of randomness in the polymer structure. The unusual strength and elongation properties of spandex-type elastomers have been theorized to be due to the uniform distribution of hard segments within the polymer matrix. Isocyanate-terminated prepolymers cannot be chain extended with aliphatic diamines neat due to the high reactivity of the ~0 diamines utilized.
Those skilled in the art are aware of the processes used to prepare spandex polymers and reference may be made, in this regard, to U.S. Pat.

Mo-6576 -11 -Nos. 3,384,623; 3,483,167; and 5,340,902, which are herein incorporated in their entireties by reference thereto.
Both aliphatic and aromatic di- and polyisocyanates may be used to prepare the prepolymers preferred in the present invention. Diisocyanates are preferred, however, it is within the scope of the invention to include a minor amount, i.e., not more than approximately 20 mole %, of a tri- or higher-functionality isocyanate. Preferred isocyanates include, but are not limited to, linear aliphatic isocyanates such as 1,2-ethylene diisocyanate, 1,3-propylene diisocyanate, 1,4-butylene diisocyanate, 1,6-hexylene diisocyanate, 1,8-octyiene diisocyanate, 1,5-diisocyanata-2,2,4-trimethylpentane, 3-oxo-1,5-pentane diisocyanate, and the like, cycloaliphatic diisocyanates such as isophorone diisocyanate, the cyclohexane diisocyanates, preferably 1,4-cyclohexane diisocyanate, fully hydrogenated aromatic diisocyanates such as hydrogenated tetramethylxylyiene diisocyanate, hydrogenated toluene diisocyanates, and hydrogenated methylene diphenylene diisocyanates and aromatic diisocyanates such as the toluene diisocyanates, particularly the 2,4-isomer, the methylene diphenylene diisocyanates, particularly 2,4' and 4,4'-methylene diphenylene diisocyanate (2,4'- and 4,4'-MDI, respectively), tetramethylxylylene diisocyanate, and the like. Other aromatic diisocyanates include the polymethylene polyphenylene polyisocyanates having functionalities greater than two. Also preferred are modified diisocyanates prepared by reacting one or more diisocyanates with themselves, or with a iow molecular weight isocyanate reactive compound to form urea-modified, urethane-modified, carbodiimide-modified, allophanate-modified, uretonimine-modified, biuret-modified, and other modified isocyanates, many of which are commercially available. More than one isocyanate may be used. Most particularly preferred is 4,4°-MDI.
An important part of the polyetherurethaneurea (PEUU) elastomer of the present invention is the isocyanate-reactive component used to prepare the isocyanate-terminated prepolymer. This component is a combination of one or more high molecular weight, ultra-low monol diols Mo-6576 -12 -and a glycol such as tripropylene glycol, dipropylene glycol, propylene glycols, diethylene glycol, triethyiene glycol, 1,3-propane diol, pentane diol, polyprapylene glycols such as PPG-425 and polytetramethylene ether glycols such as PTMEG-250 and PTMEG-650.
The high molecular weight, ultra-low unsaturated polyoxypropylene glycol and the low molecular weight diol are blended in proportion such That the number average molecular weight of the blend is between 2,000 Da and 9,000 Da and more preferably between 2,300 Da and 3,700 Da.
The number average molecular weight may be an amount ranging between any combination of these values, inclusive of the recited values.
The molecular weight of the high molecular weight, ultra-low monol diol, is preferably at least 4,000 Da, more preferably 6,000 Da, and most preferably 8,000 Da. The glycol makes up the remainder of the isocyanate-reactive component. The unsaturation of the high molecular weight polyol component is critical. Preferably, the high molecular weight poloxypcopylene glycol has an unsaturation of less than 0.010 meqlg, more preferably less than 0.007 meqlg, and most preferably 0.005 meqlg or lower.
As used herein, the term °°ultra-low mono) diol'°
means a polymer glycol prepared by oxyalkylating a dihydric initiator with an alkylene oxide in the presence of a catalyst such that the total unsaturation of the polyol product is less than 0.010 meqlg. Preferably, the catalyst is a double metal cyanide catalyst, such as those disclosed in tJ.S. Pat. I~os.
5,470,813 and 5,482,J08, the entire contents of which are incorporated herein by reference. Through the use of the catalysts disclosed in those references, polyols having the desired unsaturation levels in the range of 0.004 to 0.008 may be obtained.
Following preparation of the isocyanate-reactive component, the mixture may be reacted with an excess of the desired diisocyanate, under a nitrogen atmosphere at slightly elevated temperature, i.e., between 50°C
and 100°C more preferably between 60°C and 90°C. The reaction of the isocyanate with the isocyanate-reactive component may be catalyzed, but Mo-6576 -13 -it is generally preferred that the reaction take place without catalysis. The reaction proceeds until the isocyanate content becomes constant. The isocyanate-terminated prepolymer thus produced may be dissolved in a polar aprotic solvent such as dimethyl acetamide (DMAc), dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), N-methyl pyrrolidone (NMP), or the like, and chain-extended with the chain extender component described below Ethylene diamine (EDA) makes up one part of the chain extender component used to make the polyetherurethaneurea (PEUU) elastomer of the present invention. The other portion is preferably an aliphatic, asymmetric co-diamine such as, isophorone diamine (IPDA), 1,2-diaminopropane (PDA) and 2-methylpentamethylenediamine (available as DYTEK A from DuPont), xylene diamine and 1,3-diaminocyclohexane.
The ethylene diamine (EDA) may be at least 40 mole % and up to as much as 100 mole % of the chain extender component, more preferably 50 to 90 mole % and most preferably 60 to 80 mole %. The aliphatic, asymmetric co-diamine may be between 60 to 0 mole % of the chain extender component, more preferably 50 to 10 mole °/~, and most preferably 40 to 20 mole %. The EDA and aliphatic, asymmetric co-diamine may be present in the in an amount ranging between any combination of these values, inclusive of the recited values.
E)CAMPLES
Measurine Methods The properties of the polyetherurethaneurea (PEUU) elastomeric materials produced in the Examples were determined as follows:
(1 ) Tensile strength, percent elongation and Mod 100 were determined by ASTM D 412.

(2) Retained stress was determined by extending the film to a given percent elongation (in this case 100%). It was held at this elongation for a fixed length of time. The stress on the film was Mo-6576 - 14 -monitored as a function of time and normalized to the stress at time zero as follows:
Retained stress = (Stress Via. time, t)*100 (Stress @ t=0) The following materials were employed in making the polyetherurethaneurea (PEUU) elastomers of the examples:
Polyol A 2,000 molecular weight, ultra-tow mono! diol, available from Bayer Polymers LLC as ACCLAIM Polyol 2200;
Polyol B 4,000 molecular weight, ultra-low mono! diol, unsaturation of 0.0034 meqlg, available from Bayer Polymers LLC as ACCLAIM Polyol 4200;
Polyol C 4,000 molecular weight, conventional polypropylene glycol (PPG), unsaturation of 0.072 meqlg Polyol D 8,000 molecular weight, ultra-!ow mono! diol, having an unsaturation of 0.0049 meqlg, available from Bayer Polymers LLC as ACCLAIM Polyol 8200;
IPDA isophorone diamine, from Sigma-Aldrich;
PDA 1,2-diaminopropane, from Sigma-Aldrich;
DYTEK A 2-methylpentamethylenediamine, from DuPont;
TPG tripropylene glycol, from Sigma-Aldrich; and PTMEG 2000 MW polytetramethyiene ether glycol, available as PoIyTHF-2000 from BASF.
The general procedure used to make the polyetherurethaneurea (PEUU) elastomers of the present invention is similar to that used to make spandex polymer solutions. Briefly, a prepolymer was made by reacting an excess of 4,4'-MDI with the appropriate poiyol(s). The prepolymer was characterized by the NCO:OH ratio (equivalents of isocyanate reacted per equivalent of hydroxyl groups) and the percent NCO (wt. % of NCO groups which remained after all the hydroxyl groups have reacted, i.e., free NCO
group content). A catalyst such as DABCO T-12 (dibutyltin dilaurate) may be used to accelerate the hydroxyl-isocyanate reaction. After the hydroxyl Mo-G576 -15 -groups were fully reacted, the prepolymer was chain extended using a mixture of ethylene diamine (EDA) and one or more aliphatic_aliphatic, asymmetric co-diamines in an aprotic solvent such as dimethylacetamide (DMAc), dimethylformamide (DMF) or N-methyl-2-pyrrolidone (NMP). The percent polymer in solvent is herein referred to as the percent solids. As those skilled in the art are aware, in actual production, the percent solids must be kept at the level required to give the appropriate viscosity for the dipping of formers used to produce thin-walled articles such as gloves, condoms, etc.
The data presented herein is for thin films. Briefly, films were cast onto glass plates from the polymer solution. The films were dried and cut with a die into 0.25 in. wide strips. Tests were run on a constant-rate-of extension type tensile testing machine with a Toad capacity of 50N
(11.2 lb.). Pneumatically operated clamps gripped the samples. To avoid tearing at the grips, the films were sandwiched between two pieces of self fusing jacketing tape (Okonite Co., No. 35).
Various additives may be added to the polymer solution such as anti-oxidants, UV stabilizers, anti-tack agents, and dyes or pigments.

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Mo-6576 -17 -Retained stress after extension at 100% elongation for 8 minutes is denoted as RS (8 min.). As can be appreciated by reference-to Table I, Comparative Examples C-1 and C-2 show high modules of films made with PTMEG or the 2,000 molecular weight ultra-low monol PPG diol (4.42 and 3.83 MPa, respectively). This makes the polyetherurethaneurea (PEUU) elastomers made with PTMEG and the 2,000 molecular weight ultra-low monol PPG diol unsuitable as latex replacements. In C-5 and C-6, one can see that these formulations also gave modules values above the target of 2 MPa (3.39 and 2.57 MPa, respectively). It should be noted however, that the modules of C-6 was substantially lower than that of C-5.
This is consistent with an 8,000 molecular weight ultra-low monol diol being employed as the polyol component in C-6. A 4,000 molecular weight ultra-low monol diol was employed as the polyoi component in C-5.
The NCO contents of the prepolymers used in C-5 and C-f were both 2.46% and thus outside the scope of this invention. Example 7 exhibits the desired features of low modules, high tensile strength and high retained stress.
Examples C-10 and C-11 Table II illustrates the large effect of monol on the mechanical properties of films made with a low free NCO group content prepolymer.
Example C-10 was made with a 4,000 molecular weight ultra-low monol polyol component had high elongation and retained stress. Conversely, Example C-11 displayed very low tensile strength and elongation. In addition, the solution viscosity was too low for practical dipping of formers.
The low properties and viscosity are indicative of low overall polymer molecular weight. These results demonstrate the importance of the polyols having an ultra-low monol content to produce films and articles with the requisite characteristics.

Mo-6576 -18 -Table 11 Exam le_ Number C-10 C-11 -Pol of Pol ol_B Pol of C

Pol of MW 4,000 4,000 NCO/OH 1.70 1.70 loNCO 1.28 1.32 Prepolymer viscosity 1 g, 040 11, 560 at 50C (mPas) solids 22 22 Polymer solution viscosity17,080 125 at 50C mPas Mole ~ EDA 80 80 Mole % co-diamine PDA 20 20 Mod 100 MPa 1.37 1.57 Tensile Stren th MPa 18.5 3.0 ~ Elon ation at break 1,562 431 RS (8 min.) 84 ---Examples 12-14. C-15 and C-16 Table 111 shows the effect of the mole percent co-diamine level on modules and retained stress where DYTEK A was used as the co-diamine and the free NCO group content was 2.00°~. For the examples summarized in Table lll, an 8,000 molecular weight, ultra-low unsaturation polyoxypropylene glycol was blended with tripropylene glycol in proportion such that the number average molecular weight of the blend was 2,318 Da. Following preparation of the blend, the blend was reacted with an excess of 4,4'-MDI at 80°C in the presence of 35 ppm (based on the weight of polyols) of DABCO T-12 (dibutyltin dilaurate). The prepolymer was injected with rapid stirring into a jar containing dimethylacetamide (DMAc) and diamines such that the final polymer solutions had the percent solids and amine percentages listed in Table III. To maximize the polymer molecular weight and mechanical properties, no mono-amine terminators such as diethylamine were used. The ratio of equivalents of diamines to isocyanate was set as close as possible to 1.00. In addition, the jar contained sufficient anti-oxidant (GYANOX 1790) so that the polymer contained 0.5% anti-oxidant on a solvent-free basis.

Mo-6576 - 19 -Table 111 Ex. # 12 13 14 C-15 C-16 Polyols PolYol Pofyof Polyol Polyol Polyol D D D D D

TPG TPG TPG TPG TPG

Blend MW 2,318 2,318 2,318 2,318 25318 NCOIOH 1.65 1.65 1.65 1.65 1.65 %NCO 2.00 2.00 2.00 2.00 2.00 Prepolymer viscosity 27,110 27,110 27,110 27,350 27,350 at 50C (mPa~s) solids 22 22 22 22 22 Polymer solution 6 12,020 7,900 11,140 4,550 g30 viscosity ~
at 50C mPa~s Mole % EDA 100 75 50 25 0 Mole co-diamine --- 25 50 75 100 (DYTEK A

Mod 100 l 1.86 1.67 1.55 1.34 gg MPa .

Tensile Strength 45.'3 38.5 45.1 36.0 34.3 (MPa Elongation 1 255 1,119 1,175 1, 069 1,105 at break ' _ RS (8 min.) 87.3 79.4 ~ 66.6 As can be appreciated by reference to Tabie III, all of the formulations had the desired low 100% modulus, high tensile strengths, and elongations of greater than 1,000°~. One can see that Comparative Example C-16, which contained no EDA and 100% DYTEK A, had unacceptable retained stress.
Examples 17-19 Table IV shows the effect of the mole percent co-diamine level on modulus and retained stress where isophorone diamine (IPDA) was used as the co-diamine. For the examples summarized in Table IV, an 8,~00 molecular weight, ultra-low unsaturation polyoxypropylene glycol (ACCLAIM Polyol 8200) was blended with tripropylene glycol in proportion Mo-s57s - 20 -such that the number average molecular weight of the blend was 2,318 Da. Following preparation of the blend, the blend was reacted with an excess of 4,4'-MDI at 80°C in the presence of 35 ppm (based on the weight of polyols) of DABCO T-12 (dibutyltin dilaurate). The prepolymer was injected with rapid stirring into a jar containing dimethylacetamide (DMAc), and diamines such that the final polymer solutions had the percent solids and amine percentages listed in Table tV. To maximize the polymer molecular weight and mechanical properties, no mono-amine terminators such as diethylamine were used. The ratio of equivalents of diamines to isocyanate was set as close as possible to 1.00. In addition, the jar contained sufficient anti-oxidant (CYAN07C 1790) so that the polymer contained 0.5°!° anti-oxidant on a solvent-free basis.
Table IV
Example No. 17 18 1g _ Polyol Palyol Polyol Polyols D D D

TPG TPG TPG

Blend MiN 2,318 2,318 2 ,318 NCOIOH 1.65 1.65 _ _1.6_5 %NCO 2.00 2.00 2.00 Prepolymer viscosity at 27 27,110 27,110 mPas) , solids 22 22 22 Polymer solution viscosity6 180 5,360 at 830 2 50C mPas , , Mole /~ EDA 100 75 50 Mole ~ co-diamine IPDA --- 25 50 Mod 100 MPa 1.99 1.99 1.70 Tensile Strength (MPa) 45.3 42.4 45.4 /~ Elon ation at break 1,255 1,239 1,136 RS (8 min. 87 77 As can be appreciated by reference to Table iV, all of the formulations had the desired low 100°~ modulus, high tensile strengths and retained stress, and elongations of greater than 1,000%.

Mo-6576 - 21 -Examples 20-22 and C-23 Table V shows the effect of the mole percent co-diamine level on modulus and retained stress where DYTEK A was used as the co-diamine and the free NCO graup content was 1.60°/~. For the examples in Table V, an 8,000 molecular weight, ultra-low unsaturation polyoxypropylene glycol (ACCLAIM Polyol 8200) was blended with tripropylene glycol in proportion such that the number average molecular weight of the blend was 2,998 Da. Following preparation of the blend, the blend was reacted with an excess of 4,4'-MDI at 80°C in the presence of 35 ppm (based on the weight of polyols) of Dabco T-12 (dibutyltin dilaurate). The prepolymer was injected with rapid stirring into a jar containing dimethylacetamide (DMAc), and diamines such that the final polymer solutions had the percent solids and amine percentages listed in Table V. To maximize the polymer molecular weight and mechanical properties, no mono-amine terminators such as diethylamine were used. The ratio of equivalents of diamines to isocyanate was set as close as possible to 1.00. In addition, the jar contained sufficient anti-oxidant (CYANOX 1790) so that the polymer contained 0.5°!~ anti-oxidant on a solvent-free basis.
Table V
Exam le Number 20 21 22 C-23 r Polyols Polyol Polyoi Pofyol Poiyol D D D D
TPG TPG TPG TPG

Blend MW 2,998 2,998 2,998 2,998 NCOIOH 1.65 1.65 1.65 1.65 %NCO 1.60 1.60 1.59 1.60 Prepolymer viscosity 27,430 27,430 27,590 27,430 at 50C mPa~s) solids 22 22 22 22 Polymer solution 5,000 4,870 10,800 6,170 viscosit at 50C mPa~s Mole % EDA 100 67 50 34 Mole % co-diamine ~_ 33 50 66 (DYTEK A

Mod 100 MPa 1.67 1.50 1.31 1.20 Tensile Strength (MPa)36.2 31.5+ 28.3 33.9 Elon ation at break 1,427 1,410+ 1,201 1,295 RS 8 min. 89 87 84 73 Mo-6576 - 22 -As can be appreciated by reference to Table V, all of the formulations had the desired low 100% modulus, high tensile strengths and elongations of greater than 1,000%. Note that the 100% modulus decreases as the mole percent co-diamine increases. One can see that comparative C-23 which contained 34 mole % EDA and 66 mole °~
DYTEK A had unacceptably low retained stress at 8 minutes.
Examples 24 28 Table VI shows the effect of the mole percent co-diamine level on modulus and retained stress when 1,2-diaminopropane (PDA) was used as the co-diamine. For the examples in Table Vl, an 8,000 molecular weight, ultra-low unsaturation poiyoxypropylene glycol (ACCLAIM Polyof 8200) was blended with tripropylene glycol in proportion such that the number average molecular weight of the blend was 3,6f7 Da. Following preparation of the blend, the blend was reacted with an excess of 4,4'-MDI
at 80°C in the presence of 35 ppm (based on the weight of polyofs) of DABCO T-12 (dibutyltin diiaurate). The prepolymer was injected with rapid stirring into a jar containing dimethyiacetamide (DMAc), and diamines such that the final polymer solutions had the percent solids and amine percentages listed in Table Vi. To maximize the polymer molecular weight and mechanical properties, no mono-amine terminators such as diethylamine were used. The ratio of equivalents of diamines to isocyanate was set as close as possible to 1.00. In addition, the jar contained sufficient anti-oxidant (CYANOX 1790) so that the polymer contained 0.5°~ anti-oxidant on a solvent free basis.

Mo-6576 - 23 -Table VI
Exam le No. 24 25 26 27 28 Polyols Polyol Polyol Polyol Polyol Polyol D D D D D

TPG TPG TPG TPG TPG

Blend MW 3,667 3,667 3,667 3,667 3,667 NCOIOH 1.65 1.65 1.65 1.65 1.65 N CO 1. 34 1. 34 1.34 1.34 1.34 Prepolymer viscosity~at 32,060 32,060 32,060 32,060 32,060 50C mPa~s solids 22 22 22 22 22 Polymer solution 72 42,170 36,310 44,430 72,730 viscosity , at 50C mPa'S

Mole % EDA 70 60 50 40 30 Mole % co- 30 40 50 60 70 diamine (PDA

Mod 100 1 25 1.28 1.36 1.29 (MPa . .

Tensile Strength 32.4+ 27.9 31.3 25.6 22.6+

MPa Elongation 1 546 1,561 1,312 1,351+
470+ 1 at break , , RS 8 min.) 92 90 90 91 91 As can be appreciated by reference to Table VI, all the formulations had the desired low 100% modulus, high tensile strengths and retained stress and elongations of greater than 1,000%. The high tensile strengths are particularly surprising given the low NCO content (1.34%) of the prepolymer used to make these materials.
Examples 29-31 Table VII shows the effect of the mole percent co-diamine level on modulus and retained stress where D~TEK A was used as the co-diamine and the free NCO group content was 1.34%. For the examples in Table Vll, an 8,000 molecular weight, ultra-low unsaturation polyoxypropylene glycol (ACCLAIM Polyol 8200) was blended with tripropylene glycol in Mo-6576 - 24 -proportion such that the number average molecular weight of the blend was 3,667 Da. Following preparation of the blend, the blend was reacted with an excess of 4,4'-MDI at 80°C in the presence of 35 ppm (based on the weight of polyols) of DABCO T-12 (dibutyltin dilaurate). The prepolymer was injected with rapid stirring into a jar containing dimethylacetamide (DMAc), and diamines such that the final polymer solutions had the percent solids and amine percentages listed in Table VII.
To maximize the polymer molecular weight and mechanical properties, no mono-amine terminators such as diethylamine were used. The ratio of equivalents of diamines to isocyanate was set as close as possible to 1.00. In addition, the jar contained sufficient anti-oxidant (CYAN07C 1790) so that the polymer contained 0.5°~ anti-oxidant on a solvent-free basis.
Table VII
Ex. # _ 29 30 31 Polyols Polyol Polyol Polyol D D D
TPG TPG TPG

Blend MW 3,667 3,667 3,668 NCOIOH 1.65 1.65 1.65 %NCO 1.34 1.34 1.33 Prepolymer viscosity at 32, 060 32, 060 32, 050 mPaes solids 22 22 22 Polymer solution viscosity64,310 25,280 2,990 at 50C (mPa~s Mole lo EDA 70 60 . 50 Mole ~ co-diamine DYTEK 30 40 50 A

Mod 100 MPa 1.28 1.21 1.12 Tensile Strength (MPa) 33.4 27.5 22.2 Elon ation at break 1,314 1,136 1,702 RS (8 min.) 91 90 84 As can be appreciated by reference to Table VI(, all the formulations had the desired low 100% modulus, high tensile strengths and retained stress and elongations of greater than 1000%. Again, the high tensile strengths are particularly surprising given the low NCO content (1.34%) of the prepolymer used to make these materials.

Mo-6576 - 25 -The foregoing examples of the present invention are offered for the purpose of illustration and not limitation. It will be apparent to those skilled in the art that the embodiments described herein may be modified or revised in various ways without departing from the spirit and scope of the invention. The scope of the invention is to be measured by the appended claims.

Claims (54)

1. An amine-extended polyetherurethaneurea (PEUU) elastomer comprising the reaction product of:
a) an isocyanate-terminated prepolymer having a free NCO
group content of from about 1 to about 2%, which is the reaction product of, (i) a stoichiometric excess of at least one isocyanate, (ii) an isocyanate-reactive component containing a blend of a glycol and one or more ultra-low monol diols having a molecular weight of at least about 4,000 Da and an unsaturation of less than about 0.010 meq/g, and optionally, (iii) a catalyst;
with b) a mixture of at least about 40 mole % of ethylene diamine (EDA) and up to about 60 mole % of at least one aliphatic, asymmetric co-diamine, wherein reaction of a) and b) is carried out in a polar, aprotic solvent.

2. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the glycol is chosen from tripropylene glycol (TPG), dipropylene glycol (DPG), propylene glycol (PG), polypropylene glycol (PPG) and polytetramethylene ether glycol (PTMEG).

3. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the blend has a number average molecular weight of between about 2,000 Da and about 9,000 Da.

4. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the blend has a number average molecular weight of between about 2,300 Da and about 3,700 Da.

5. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the one or more ultra-low monol diols has a molecular weight of at least about 6,000 Da.

6. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the one or more ultra-low monol diols has a molecular weight of at least about 8,000 Da.

7. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the glycol is tripropylene glycol (TPG).

8. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the unsaturation of the one or more ultra-low monol diols is less than about 0.007 meq/g.

9. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the unsaturation of the one or more ultra-low monol diols is less than about 0.005 meq/g.

10. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the at least one isocyanate is chosen from 1,2-ethylene diisocyanate, 1,3-propylene diisocyanate, 1,4-butylene diisocyanate, 1,6-hexylene diisocyanate, 1,8-octylene diisocyanate, 1,5-diisocyanato-2,2,4-trimethylpentane, 3-oxo-1,5-pentane diisocyanate, isophorone diisocyanate, the cyclohexane diisocyanates, hydrogenated tetramethylxylylene diisocyanate, hydrogenated toluene diisocyanates, hydrogenated methylene diphenylene diisocyanates, toluene diisocyanates, the methylene diphenylene diisocyanates and the polymethylene polyphenylene polyisocyanates.

11. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the at least one isocyanate is 4,4'-methylene diphenylene diisocyanate (4,4'-MDI).

12. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the mixture b) contains about 50 to about 90 mole % of ethylene diamine (EDA) and about 10 to about 50 mole % of at least one aliphatic, asymmetric co-diamine.

13. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the mixture b) contains about 60 to about 80 mole % of ethylene diamine (EDA) and about 20 to about 40 mole % of at least one aliphatic, asymmetric co-diamine.

14. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the at least one aliphatic, asymmetric co-diamine is chosen from isophorone diamine (IPDA), 1,2-diaminopropane (PDA), 2-methylpentamethylenediamine, xylene diamine and 1,3-diaminocyclohexane.

15. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the at least one aliphatic, asymmetric co-diamine is 1,2-diaminopropane (PDA).

16. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the at least one aliphatic, asymmetric co-diamine is 2-methylpentamethylenediamine.

17. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the at least one aliphatic, asymmetric co-diamine is isophorone diamine (IPDA).

18. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1, wherein the polar, aprotic solvent is chosen from dimethyl acetamide (DMAc), dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), N-methyl pyrrolidone (NMP).

19. The amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1 further including one or more additives chosen from anti-oxidants, UV stabilizers, anti-tack agents, dyes and pigments.

20. A process for making an amine-extended polyetherurethaneurea (PEUU) elastomer comprising:
reacting a) an isocyanate-terminated prepolymer having a free NCO
group content of from about 1 to about 2 %, which is the reaction product of, (i) a stoichiometric excess of at least one isocyanate, (ii) an isocyanate-reactive component containing a blend of a glycol and one or more ultra-low monol diols having a molecular weight of at least about 4,000 Da and an unsaturation of less than about 0.010 meq/g, and optionally, (iii) a catalyst;
with b) a mixture of at least about 40 mole % of ethylene diamine (EDA) and up to about 60 mole % of at least one aliphatic, asymmetric co-diamine, in a polar, aprotic solvent, and collecting the reaction product.

21. The process according to Claim 20, wherein the glycol is chosen from tripropylene glycol (TPG), dipropylene glycol (DPG), propylene glycol (PG), polypropylene glycol (PPG) and polytetramethylene ether glycol (PTMEG).

22. The process according to Claim 20, wherein the blend has a number average molecular weight of between about 2,000 Da and about 9,000 Da.

23. The process according to Claim 20, wherein the blend has a number average molecular weight of between about 2,300 Da and about 3,700 Da.

24. The process according to Claim 20, wherein the one or more ultra-low monol diols has a molecular weight of at least about 6,000 Da.

25. The process according to Claim 20, wherein the one or more ultra-low monol diols has a molecular weight of at least about 8,000 Da.

26. The process according to Claim 20, wherein the glycol is tripropylene glycol (TPG).

27. The process according to Claim 20, wherein the unsaturation of the one or more ultra-low monol diols is less than about 0.007 meq/g.

28. The process according to Claim 20, wherein the unsaturation of the one or more ultra-low monol diols is less than about 0.005 meq/g.

29. The process according to Claim 20, wherein the at least one isocyanate is chosen from 1,2-ethylene diisocyanate, 1,3-propylene diisocyanate, 1,4-butylene diisocyanate, 1,6-hexylene diisocyanate, 1,8-octylene diisocyanate, 1,5-diisocyanato-2,2,4-trimethylpentane, 3-oxo-1,5-pentane diisocyanate, isophorone diisocyanate, the cyclohexane diisocyanates, hydrogenated tetramethylxylylene diisocyanate, hydrogenated toluene diisocyanates, hydrogenated methylene diphenylene diisocyanates, toluene diisocyanates, the methylene diphenylene diisocyanates and the polymethylene polyphenylene polyisocyanates.

30. The process according to Claim 20, wherein the at least one isocyanate is 4,4'-methylene diphenylene diisocyanate (4,4'-MDI).

31. The process according to Claim 20, wherein the mixture b) contains about 50 to about 90 mole % of ethylene diamine (EDA) and about 10 to about 50 mole % of at least one aliphatic, asymmetric co-diamine.

32. The process according to Claim 20, wherein the mixture b) contains about 60 to about 80 mole % of ethylene diamine (EDA) and about 20 to about 40 mole % of at least one aliphatic, asymmetric co-diamine.

33. The process according to Claim 20, wherein the at least one aliphatic, asymmetric co-diamine is chosen from isophorone diamine (IPDA), 1,2-diaminopropane (PDA) and 2-methyl-pentamethylenediamine, xylene diamine and 1,3-diaminocyclohexane.

34. The process according to Claim 20, wherein the at least one aliphatic, asymmetric co-diamine is 1,2-diaminopropane (PDA).

35. The process according to Claim 20, wherein the at least one aliphatic, asymmetric co-diamine is 2-methylpentamethylenediamine.

36. The process according to Claim 20, wherein the at least one aliphatic, asymmetric co-diamine is isophorone diamine.

37. The process according to Claim 20, wherein the polar, aprotic solvent is chosen from dimethyl acetamide (DMAc), dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), N-methyl pyrrolidone (NMP).

38. The process according to Claim 20 further including adding one or more additives chosen from anti-oxidants, UV stabilizers, anti-tack agents, dyes and pigments.

39. In a method of making one of a medical glove, a scientific glove and a condom, the improvement comprising including the amine-extended polyetherurethaneurea (PEUU) elastomer according to Claim 1.

40. One of a medical glove, a scientific glove and a condom made by the process according to Claim 39.

41. An isocyanate-terminated prepolymer having a free NCO group content of from about 1 to about 2 %, which is the reaction product of, (i) a stoichiometric excess of at least one isocyanate, (ii) an isocyanate-reactive component containing a blend of a glycol and one or more ultra low monol diols having a molecular weight of at least about 4,000 Da and an unsaturation of less than about 0.010 meq/g, and optionally, (iii) a catalyst.

42. The isocyanate-terminated prepolymer according to Claim 41, wherein the glycol is chosen from tripropylene glycol (TPG), dipropylene glycol (DPG), propylene glycol (PG), polypropylene glycol (PPG) and polytetramethylene ether glycol (PTMEG).

43. The isocyanate-terminated prepolymer according to Claim 41, wherein the blend has a number average molecular weight of between about 2,000 Da and about 9,000 Da.

44. The isocyanate-terminated prepolymer according to Claim 41, wherein the blend has a number average molecular weight of between about 2,300 Da and about 3,700 Da.

45. The isocyanate-terminated prepolymer according to Claim 41, wherein the one or more ultra-low monol diols has a molecular weight of at least about 6,000 Da.

46. The isocyanate-terminated prepolymer according to Claim 41, wherein the one or more ultra-low monol diols has a molecular weight of at least about 8,000 Da.

47. The isocyanate-terminated prepolymer according to Claim 41, wherein the glycol is tripropylene glycol (TPG).

48. The isocyanate-terminated prepolymer according to Claim 41, wherein the unsaturation of the one or more ultra low monol diols is less than about 0.007 meq/g.

49. The isocyanate-terminated prepolymer according to Claim 41, wherein the unsaturation of the one or more ultra low monol diols is less than about 0.005 meq/g.

50. The isocyanate-terminated prepolymer according to Claim 41, wherein the at least one isocyanate is chosen from 1,2-ethylene diisocyanate, 1,3-propylene diisocyanate, 1,4-butylene diisocyanate, 1,6-hexylene diisocyanate, 1,8-octylene diisocyanate, 1,5-diisocyanato-2,2,4-trimethylpentane, 3-oxo-1,5-pentane diisocyanate, isophorone diisocyanate, the cyclohexane diisocyanates, hydrogenated tetramethylxylylene diisocyanate, hydrogenated toluene diisocyanates, hydrogenated methylene diphenylene diisocyanates, toluene diisocyanates, the methylene diphenylene diisocyanates and the polymethylene polyphenylene polyisocyanates.

51. The isocyanate-terminated prepolymer according to Claim 41, wherein the at least one isocyanate is 4,4'-methylene diphenylene diisocyanate (4,4'-MDI).

52. The isocyanate-terminated prepolymer according to Claim 41 further including one or more additives chosen from anti-oxidants, UV
stabilizers, anti-tack agents, dyes and pigments.

53. In a method of making one of a medical glove, a scientific glove and a condom, the improvement comprising including the isocyanate-terminated prepolymer according to Claim 41.

54. One of a medical glove, a scientific glove and a condom made by the process according to Claim 53.