Lightly cross-linked polyurethane hydrogels based on poly(alkylene ether) polyols
First Claim
1. A water swellable, lightly crosslinked, hydrogel polymer of the isocyanato terminated prepolymer comprising the reaction product of:
- i. a poly(alkyleneoxy) polyol having an average molecular weight up to about 25,000 wherein the alkyleneoxy group contains from two to four carbon atoms, andii. an organic diisocyanate,said prepolymer lightly crosslinked with an equivalent amount of a crosslinking agent of the group;
iii. water or organic polyamine;
wherein said poly(alkyleneoxy) polyol is a mixture of a major amount of a poly(ethyleneoxy) diol having an average molecular weight of from about 4,000 to about 25,000, and a minor amount of a higher polyol of the group poly(alkyleneoxy) triol or poly(alkyleneoxy) tetrol or aliphatic polyhydroxyl compound of the formula Cn H2n+2-m (OH)m wherein n has a value of 3 to 6 and m has a value of 3 to 4, or mixtures thereof, said triol or tetrol having an average molecular weight of from about 92 to 5,000, wherein the mole ratio of diol to higher polyol in said mixture is from about 6;
1 to 40;
1;
wherein the equivalents ratio of isocyanato groups to hydroxyl groups is from about 1.2;
1 to about 1.6;
1;
wherein the organic polyamine is a primary or secondary diamine or triamine; and
wherein the equivalents of reactive crosslinking groups in said crosslinking agent used is equivalent to the number of equivalents of isocyanato groups present in said prepolymer.
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Abstract
Polyurethane hydrogels of high water swellability comprising lightly crosslinked polymers of isocyanate terminated prepolymers which are the reaction production of (i) poly(alkyleneoxy) polyols with (ii) organic diisocyanates that has been lightly crosslinked with (iii) water or an organic polyamine.
The use of fibrous materials as absorbents for moisture is a well known, widespread practice. In this application many of the natural and synthetic fibers have been used and extensive efforts have been made to improve the absorption properties of the materials. One of the major deficiencies of the natural and synthetic materials heretofore used has been the tendency for them to release the absorbed moisture when pressure has been applied to the moisture containing material. The fact that pressure causes the absorbed fluid to be expelled from the fibers is known as reversible absorption. For many applications, however, irreversible absorption is desired, for example, in surgical dressings, diapers, bed pads, catamenials, and the like, whereby the absorbed moisture is retained in the absorbent material under an applied pressure.
Within the past few years recent innovations have resulted in the production of materials having such irreversible absorption properties; these materials are now known as hydrogels. In most instances they have been produced in powder or particulate form and even, in some instances, in film form. An especially interesting characteristic of the hydrogel polymers is that when in contact with water they absorb it and swell to a certain point and stop and the final swollen polymer is still similar in shape to its initial unswollen shape. Many of the hydrogels have the ability to absorb many times their original weight in water without becoming soggy or deformed. In general, the hydrogels are used in conjunction with other materials as supports. Among the U.S. patents that have issued in this field are U.S. Pat. Nos. 3,669,103; 3,589,364; 3,694,301; 3,670,731; and 3,164,565. This is but an exemplary listing and should not be considered complete.
Water swellable, lightly crosslinked, hydrogel polymers of an isocyanato terminated prepolymer comprising the reaction product of (i) poly(alkyleneoxy) polyol having an average molecular weight up to about 25,000 with (ii) organic diisocyanate wherein said prepolymer is lightly crosslinked with (iii) a crosslinking agent that is water or an organic polyamine, the amount of crosslinking agent used being an equivalent amount based on the number of equivalents of isocyanato groups present in the prepolymer.
The poly(alkyleneoxy) polyols that are used in producing the hydrogel polymers of the present invention are those having a molecular weight up to about 25,000. These polyols can be diols, triols or tetrols, with the molecular weight of the polyol varying depending upon which is used.
The suitable diols are the poly(ethyleneoxy) glycols which have a molecular weight of from about 4,000 to 25,000, preferably from about 6,000 to 20,000. These diols are well known and many are commercially available. Minor amounts, preferably up to about 35 weight percent of a poly(propyleneoxy) glycol or a poly(butyleneoxy) glycol can also be present. The polyols can be block or random copolymers containing mixtures of ethyleneoxy, propyleneoxy, or butyleneoxy units.
The triols and tetrols that can be used are those having a molecular weight of from about 92 to 5,000, preferably from about 500 to 1,500. These can be the poly(alkyleneoxy) polyols wherein the alkyleneoxy group contains 2 to 4 carbon atoms and they can be homopolymers or block or random copolymers having three or four reactive hydroxyl groups. One can also use the aliphatic polyhydroxyl compounds of the formula Cn H2n+2-m (OH)m wherein n is an integer having a value of from 3 to 6 and m has a value of 3 or 4.
Illustrative of the suitable polyols are poly(ethyleneoxy) diol, poly(propyleneoxy) diol, poly(butyleneoxy) diol, copoly(ethyleneoxy-propyleneoxy) diol, poly(ethyleneoxy) triol, poly(ethyleneoxy) tetrol, poly(propyleneoxy) triol, copoly(ethyleneoxy-propyleneoxy) triol, copoly(ethyleneoxy-butyleneoxy) triol, glycerine, sorbitol, 1,2,6-hexanetriol, trimethylolpropane, pentaerythritol, dipentaerythritol, and the like. The alkylene adducts of the mono or polyamines such as ethylamine, ethanolamine, diethanolamine, ethylene-diamine, propylenediamine, isopropanolamine, hexamethylenediamine, and the like. Mixtures thereof can be used if desired. In addition, one can include some polycaprolactonepolyol, or conventional polyester polyol.
The hydrogels can be produced by reacting the poly(alkyleneoxy) diol with an organic diisocyanate to form an isocyanato terminated prepolymer which is then lightly crosslinked with a crosslinking agent that is a mixture of an organic diamine and an organic triamine. In another embodiment, the hydrogels can be produced by reacting a mixture of poly(alkyleneoxy) diols and poly(alkyleneoxy) triols and/or tetrols with an organic diisocyanate to form the prepolymer which is then lightly crosslinked with a crosslinking agent that is water, an organic diamine, or a mixture thereof. When a mixture of polyols is used in producing the hydrogels the mole ratio of the diol to the higher polyols is at least about 6:1 and can be as high as about 40:1. Preferably this mole ratio is from about 15:1 to about 30:1, and more preferably from about 20:1 to about 25:1. It has been observed that the mole ratio of diol to higher polyol has an effect on water uptake; the higher the mole ratio, the higher the water uptake.
Any of the known organic diisocyanates can be used in the reaction with the polyol to produce the isocyanato terminated prepolymer. These isocyanates are well known to those skilled in the polyurethane art and illustrative thereof one can mention, tolylene diisocyanate, phenylene diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, methylenebis(4-phenylisocyanate), 4,4'"'"'-methylene bis(cyclohexylisocyanate), 4,4'"'"'-methylene bis(o-tolylene isocyanate), dimer acid diisocyanate, 4,4'"'"'-methylene bis(phenyleneisocyanate), 2,2,4-trimethylpentane diisocyanate, aniline-formaldehyde polyisocyanates having an average of from about two to about three isocyanato groups per molecule.
In producing the isocyanato terminated prepolymer one reacts an excess of the isocyanate with the polyol. The ratio of isocyanato groups to hydroxyl is from about 1.2 to 1.6 equivalents of isocyanato per equivalent of hydroxyl. An equivalent amount of isocyanato sufficient to react with any water present in the reactants can also be added. It has been observed that at lower ratios the hydrogel polymer becomes too soluble, while at ratios above 1.6:1 the water uptake of the hydrogel decreases. In this reaction any of the known catalysts can be used such as dibutyltin dilaurate, stannous octoate, triethylenediamine, lead octoate, bis(dimethylamino) ethyl ether, and the like. The catalyst is present at a concentration of from about 0.001 to about 1 percent by weight. The conventional catalytic amounts are employed.
Production of the isocyanato terminated prepolymer is carried out in the presence of an inert organic solvent such as benzene, toluene, trichloroethane, trichloroethylene, bis(2-chloroethyl) ether, methyl ethyl ketone, ethylene dichloride, ethyl acetate, xylene, and the like.
The temperature at which the prepolymer is produced can vary from about 50°C. to about 170°C. and is not critical to the reaction. The time required to carry the reaction the completion will vary depending upon the particular reactants and catalyst used, the size of the batch and other factors known to those skilled in the art. The reaction for the preparation of the prepolymer is preferably carried out under anhydrous conditions and under an inert gas atmosphere.
The product obtained in this first step is an isocyanato terminated prepolymer that is soluble in the organic solvent used in carrying out the reaction. This solution has a solids content dependent upon the amount of materials initially charged. For ease in further handling it is preferred that the solids content be not greater than about 40 weight percent, preferably from 25 to 35 weight percent. The solution viscosity should range from about 15,000 to about 200,000 centipoises.
To produce the hydrogel polymer from the above isocyanato terminated prepolymer, one reacts this prepolymer with a crosslinking agent to effect a light degree of crosslinking. The term lightly crosslinked hydrogel polymer signifies a hydrogel that contains not more than an average of about one crosslink unit per 50,000 average molecular weight of the hydrogel. Preferably there is an average of about one crosslink unit for each 100,000 to 300,000 hydrogel molecular weight and more preferably about one crosslink unit for each 150,000 to 250,000 hydrogel molecular weight. As previously indicated, the suitable crosslinkers are water or the organic polyamines, such as the primary or secondary diamines or triamines. The polyamines can be any of the known aliphatic or aromatic polyamines such as ethylene diamine, diethylene triamine, propylene diamine, hexamethylene diamine, methylene bis(aniline), tolylene diamine, isophorone diamine, trimethylpentane diamine, aniline-formaldehyde adduct polyamines, and the like. The amount of crosslinking agent used is an amount sufficient to react with all of the terminal isocyanato groups and to effect a light crosslinking. The desired concentration of crosslinker is that wherein the equivalents of reactive crosslinking groups in the crosslinking agent used is equivalent to the number of equivalents of isocyanato groups present in the prepolymer. This amount should be sufficient to react with all of the isocyanato groups and crosslink the polymer but it should not be an amount which would result in end-capping of the isocyanato groups rather than crosslinking.
113 Citations
45 Claims
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1. A water swellable, lightly crosslinked, hydrogel polymer of the isocyanato terminated prepolymer comprising the reaction product of:
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i. a poly(alkyleneoxy) polyol having an average molecular weight up to about 25,000 wherein the alkyleneoxy group contains from two to four carbon atoms, and ii. an organic diisocyanate, said prepolymer lightly crosslinked with an equivalent amount of a crosslinking agent of the group; iii. water or organic polyamine; wherein said poly(alkyleneoxy) polyol is a mixture of a major amount of a poly(ethyleneoxy) diol having an average molecular weight of from about 4,000 to about 25,000, and a minor amount of a higher polyol of the group poly(alkyleneoxy) triol or poly(alkyleneoxy) tetrol or aliphatic polyhydroxyl compound of the formula Cn H2n+2-m (OH)m wherein n has a value of 3 to 6 and m has a value of 3 to 4, or mixtures thereof, said triol or tetrol having an average molecular weight of from about 92 to 5,000, wherein the mole ratio of diol to higher polyol in said mixture is from about 6;
1 to 40;
1;
wherein the equivalents ratio of isocyanato groups to hydroxyl groups is from about 1.2;
1 to about 1.6;
1;
wherein the organic polyamine is a primary or secondary diamine or triamine; and
wherein the equivalents of reactive crosslinking groups in said crosslinking agent used is equivalent to the number of equivalents of isocyanato groups present in said prepolymer. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45)
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Specification
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- Resources
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Current AssigneeUnion Carbide Corporation (Dow, Inc.)
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Original AssigneeUnion Carbide Corporation (Dow, Inc.)
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InventorsMatthews, Virgil Edison, Knopf, Robert John
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Primary Examiner(s)Cockeram, H. S.
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Application NumberUS05/480,568Time in Patent Office609 DaysField of Search260/77.5 AN, 260/77.5 AP, 260/2.5 AD, 260/2.5 AY, 260/77.5 AM, 11/33.8 JB, 161/159US Class Current528/60CPC Class CodesA61L 15/60 Liquid-swellable gel-formin...C08G 18/4833 Polyethers containing oxyet...C08G 2210/00 Compositions for preparing ...C08L 75/04 PolyurethanesY10S 428/904 Artificial leatherY10S 521/905 Hydrophilic or hydrophobic ...
