Patent Application
20120016046
The present invention relates to viscoelastic polyurethane foam formulations, viscoelastic polyurethane foams formed from such formulations, and products formed from the viscoelastic polyurethane foams.
Flexible, viscoelastic polyurethane foam (also known as “dead” foam, “slow recovery” foam, or “high damping” foam) is characterized by slow, gradual recovery from compression. While most of the physical properties of viscoelastic foams resemble those of conventional foams, the resilience of viscoelastic foams is much lower, generally less than about 15%. Suitable applications for viscoelastic foam take advantage of its shape conforming, energy attenuating, and sound damping characteristics. For example, the foam can be used in mattresses to reduce pressure points, in athletic padding or helmets as a shock absorber, and in automotive interiors for soundproofing.
Because of the uses of products produced from viscoelastic flexible polyurethane foams, it is desirable that these products have flame retardant qualities.
In one embodiment, the present invention relates to a flexible viscoelastic polyurethane foam formulation comprising a) a flame retarding amount of i) one or more chlorinated phosphate esters, ii) one or more brominated flame retardants, iii) one or more phosphorous-based halogen-free flame retardants, or iv) combinations of i), ii) and/or iii), b) at least one isocyanate having a functionality of at least two; c) at least one polyalkyleneoxide diol wherein in the range of from about 50% to about 95% of the terminal OH groups of the diol are primary OH groups; and, optionally, d) one or more i) surfactants, ii) antioxidants, iii) diluents, iv) chain extenders or cross linkers, v) synergists, preferably melamine; vi) plasticizers, vii) catalysts, viii) water, ix) alternative blowing agents like methylene chloride, x) pigments, xi) cell-openers, xii) other ancillary chemicals used by those skilled in the art of making flexible polyurethane foam.
In another embodiment, the present invention relates to a method for forming a flexible viscoelastic polyurethane foam comprising bringing together in the presence of one or more catalysts: a) a flame retarding amount of i) one or more chlorinated phosphate esters, ii) one or more brominated flame retardants, iii) one or more phosphorous-based halogen-free flame retardants or iv) combinations of i), ii) and/or iii), b) at least one isocyanate having a functionality of at least two; c) at least one polyalkyleneoxide diol wherein in the range of from about 50% to about 95% of the terminal OH groups of the diol are primary OH groups; and, optionally, d) one or more i) surfactants, ii) antioxidants, iii) diluents, iv) chain extenders or cross linkers, v) synergists, preferably melamine; vi) plasticizers, vii) water, viii) alternative blowing agents like methylene chloride, ix) pigments, x) cell-openers xi) other ancillary chemicals used by those skilled in the art of making flexible polyurethane foam.
In another embodiment, the present invention relates to a flexible viscoelastic polyurethane foam formulation derived or derivable from: a) a flame retarding amount of i) one or more chlorinated phosphate esters, ii) one or more brominated flame retardants, iii) one or more phosphorous-based halogen-free flame retardants or iv) combinations of i), ii) and/or iii), b) at least one isocyanate having a functionality of at least two; c) at least one polyalkyleneoxide diol wherein in the range of from about 50% to about 95% of the terminal OH groups of the diol are primary OH groups; and, optionally, d) one or more i) surfactants, ii) antioxidants, iii) diluents, iv) chain extenders or cross linkers, v) synergists, preferably melamine; vi) plasticizers, vii) catalysts, viii) water, ix) alternative blowing agents like methylene chloride, x) pigments, xi) cell-openers, xii) other ancillary chemicals used by those skilled in the art of making flexible polyurethane foam.
In other embodiments, the present invention relates to articles made from the flexible viscoelastic polyurethane foam formulations of the present invention.
As stated above, common technology used to manufacture viscoelastic polyurethane foams relies on defects in the polyurethane network structure, i.e. “dangling chains”. Currently, the creation of defects in the foam is obtained through the use of formulations designed to have a shortage of isocyanate groups. By proceeding in this fashion, the foam producers insures that, after the reaction between the isocynate and polyol, some hydroxy groups borne by the polyol molecules remain unreacted in the foam thus formed. The unreacted hydroxy groups are the “dangling chains” that create the desired “slow recovery” characteristics of the viscoelastic polyurethane foams. More recent viscoelastic foam technologies have been developed that are based on the use of polyol blends containing a large proportion of mono-functional (i.e. monols). After reaction completion, these monols act as dangling materials and impart the foam with the desired visco-elastic properties. Such monols containing polyol blends do allow the use of higher concentration of isocyanate, sometimes approaching the 100 isocyanate index. The inventors hereof have discovered, however, that by using specific diols, such as those described herein, and the flame retardants described herein, a flexible viscoelastic polyurethane foam or foam formulation can be produced without creating dangling chains, i.e. without using a formulation designed to insure a shortage of isocynate groups, sometimes called a 100 isocyanate index. This is a particularly desired quality of the foams of the present invention because upon burning, these dangling chains induce a severe dripping making it extremely difficult, in some instances bordering impossible, even with large loadings of flame retardants and synergists, to meet fire standards like BS5852 crib 5 where the weight loss occurring during burning is a test criteria. In addition, adding large loadings of solid flame retardant synergist like melamine eliminates the foam's desired slow recovery behavior without bringing significant flame retardance improvement, nor meeting consistent positive results in fire standard tests like BS5852 crib 5.
Isocyanates suitable for use in the present invention include any isocyanate used in the production of flexible polyurethane foams. These isocyanates, most preferred diisocyanates, are well known components of polyurethane foams and polyurethane foam formulations and include any compounds which possess at least one free cyanate reactive group, and most preferably two, although more may be utilized. Such compounds may also be aliphatic or aromatic in nature. Non-limiting examples of isocyanates suitable for use in the present invention include aromatic, aliphatic, and cycloaliphatic polyisocyanates and combinations thereof such as m-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, mixtures of 2,4- and 2,6-toluene diisocyanate, hexamethylene diisocyanate, tetramethylene diisocyanate, cyclohexane-1,4-diisocyanate, hexahydrotoluene diisocyanate (and isomers), naphthalene-1,5-diisocyanate, 1-methoxyphenyl-2,4-diisocyanate, 4,4′-diphenylmethane diisocyanate, 4,4′-biphenylene diisocyanate, 3,3′-dimethoxy-4,4′-biphenyl diisocyanate, 3,3′-dimethyl-4,4′-biphenyl diisocyanate and 3,3′-dimethyldiphenylmethane-4,4′-diisocyanate; the triisocyanates such as 4,4′,4″-triphenylmethane triisocyanate, and toluene 2,4,6-triisocyanate; and the tetraisocyanates such as 4,4′-dimethyldiphenylmethane-2,2′,5,5′-tetraisocyanate and polymeric polyisocyanates such as polymethylene polyphenylene polyisocyanate. Crude polyisocyanates may also be used in the compositions of the present invention, such as crude toluene diisocyanate obtained by the phosgenation of a mixture of toluene diamines or crude diphenylmethane isocyanate obtained by the phosgenation of crude diphenylmethanediamine. These crude isocyanates are disclosed in U.S. Pat. No. 3,215,652.
The most prominently utilized isocyanates, and thus the most preferred types for this invention (though not required), are toluene diisocyanate (“TDI”), diphenylmethane diisocyanate (“MDI”) or methylene diisocyanate (others, such as aliphatic isocyanates may be utilized, as well as other aromatic types). The polyol is generally reacted with a slight excess of isocyanate (hydroxyl OH groups on isocyanate NCO groups ratio of from 1:0.85 to 1:1.40) to produce a soft flexible foam product; the greater the ratio, the harder the produced foam).
The diols suitable for use in the present invention can be either polyether or polyester diols. The diols used in the practice of the present invention are those wherein in the range of from about 50% to about 95% of the OH groups of the diol are primary OH groups. In preferred embodiments, the diols are those wherein in the range of from about 65% to about 90%, more preferably in the range of from about 70% to about 85%, of the OH groups of the diol are primary OH groups.
The diols suitable for use herein can also be described as having a number average molecular weight of greater than 1000 g/mole, preferably in the range of from about 1000 g/mole to about 4000 g/mole, more preferably in the range of from about 1500 g/mole to about 3000 g/mole.
Preferred diols are polyoxyalkylene diols. In some embodiments, the polyoxyalkylene diols can have any desired arrangement of polyoxyalkylene units. For example, the polyoxyalkylene diols can be Propylene Oxide (“PO”)-based homopolymers, block Ethylene Oxide (“EO”)-PO copolymers, random EO/PO copolymers, PO-based polyols that are “capped” or “tipped” with a mixture EO and PO to achieve a desired primary hydroxyl content, or any other desired configuration. In a particularly preferred embodiment, the polyalkylkene diol used in the practice of the present invention is a PO-based polyol tipped with EO to achieve the desired primary hydroxyl content. In some embodiments, the polyalkylene diols used in the practice of the present invention are those having a percentage of EO added as a “tip” on total PO+EO added during manufacturing in the range of from about 1% to about 20%, preferably of from about 5% to about 15%, more preferably from about 9% to 13%.
The viscoelastic formulations of the present invention also contain a flame retardant, in some embodiments a flame retarding amount of a flame retardant, selected from i) one or more chlorinated phosphate esters, ii) one or more brominated flame retardants, iii) one or more phosphorous-based halogen-free flame retardants or iv) combinations of i), ii) and/or iii). By a flame retarding amount, it is meant that amount sufficient to meet or exceed the test standards set forth in BS5852 flammability test. Generally, depending on the foam density, this is in the range of from about 5 to about 50 parts per hundred parts of polyol(s) (“php”) of the flame retardant additive. In preferred embodiments, a flame retarding amount is to be considered in the range of from about 10 to about 35 php more preferably in the range of from about 12 to about 25 php.
Chlorinated Phosphate esters suitable for use herein can be selected from any chlorinated phosphate esters, which are conventionally used in the art of making flexible, flame retarded polyurethane foams.
Specific examples of suitable chlorinated phosphate esters used in exemplary embodiments are: tris(1,3-dichloropropyl)phosphate; also known as TDCP, tris(2-chloropropyl)phosphate, also known as TCPP or TMCP, 2,2-bis(chloromethyl)1,3 propylene bis[di(2-chloroethyl)phosphate], also known as V6, tris(2-chloroethyl)phosphate, also known as TCEP.
In these embodiments, the chlorinated phosphate esters used in the present invention typically contain in the range of from about 5 to about 15wt % organic phosphorous, based on the total weight of the phosphate ester. Preferably, the organic phosphorus content is in the range of from about 6 to about 13wt %, on the same basis, and in more preferred embodiments the organic phosphorous content is in the range of from about 7 to about 12 wt %, on the same basis.
In these embodiments, the chlorinated phosphate esters used in the present invention typically contain in the range of from about 20 to about 60wt % chlorine, based on the total weight of the phosphate ester. Preferably, the chlorinated phosphate esters contain in the range of from about 30 to about 50wt %, of chlorine, on the same basis.
Bromine containing flame retardants suitable for use in the of the invention can be either reactive or non reactive, i.e. they react or not with the isocyanate and can be selected from any of those used in the art of making flame retarded polyurethane foams.
Specific examples of suitable brominated flame retardants used in exemplary embodiments are reactive bromine containing diester/ether diol of tetrabromophtalic anhydride. A commercial example of this class of products is Saytex® RB-79.
In these embodiments, the brominated flame retardants for use in the present invention typically contain in the range of from about 10 to about 70 wt % bromine, based on the total weight of the brominated flame retardant. Preferably, the bromine content is in the range of about 25 to about 60wt %, on the same basis. In more preferred embodiments, the bromine content of the brominated flame retardant is in the range of about 35 to about 55wt %, based on the total weight of the brominated flame retardant.
Phosphorous-based halogen free flame retardants suitable for use in the invention can be reactive non reactive, i.e. they react or not with the isocyanate, and can be selected from any of those used in the art of making flame retarded polyurethane foams. Typical classes of suitable phosphorous-based halogen free flame retardants for use in the invention are phosphates, phosphonates, phosphites, phosphinates as well as aminoalkyl compounds thereof.
In these embodiments, the phosphorous-based halogen-free flame retardants typically contain in the range of from about 5 to about 40 wt % phosphorous, based on the total weight of the phosphorous-based halogen-free flame retardant. Preferably, the phosphorous content is in the range of about 10 to about 30 wt %, on the same basis.
The viscoelastic foam formulations of the present invention can include, and in some embodiments do include, one or more i) surfactants, ii) antioxidants, iii) diluents, iv) chain extenders or cross linkers, v) synergists, preferably melamine; vi) plasticizers, vii) catalysts, viii) water, ix) alternative blowing agents like methylene chloride, x) pigments, xi) cell-openers, xii) other ancillary chemicals used by those skilled in the art of making flexible polyurethane foam. In some embodiments, one or more i) surfactants, ii) antioxidants, iii) diluents, iv) chain extenders or cross linkers, v) synergists, preferably melamine; vi) plasticizers, vii) catalysts, viii) water, ix) alternative blowing agents like methylene chloride, x) pigments, or xi) cell-openers. These optional components are well known in the art and the amount of these optional components is conventional and not critical to the instant invention.
Usable chain extenders and/or cross-linkers are diols and/or triols with molecular weights lower than 250 and particularly between 50 and 200. Usable diols are aliphatic, cycloaliphatic or aromatic types, e.g., ethylene glycol, diethylene glycol, dipropylene glycol, and 1,4 butanediol. Usable triols include, for example, trimethylolpropane and glycerine.
Examples of suitable surfactants are emulsifiers such as sodium salts of castor oil sulfates or fatty acids; fatty acid salts with amines, e.g., diethylamine oleate and diethanolamine stearate; salts of sulfonic acids, e.g., alkali metal or ammonium salts of dodecylbenzenedisulfonic acid and ricinoleic acid; foam stabilizers such as siloxaneoxyalkylene copolymers and other organopolysiloxanes, ethoxylated alkylphenols, ethoxylated fatty alcohols and castor oil. Other suitable surfactants are organosilicone surfactants.
Suitable plasticizers include dioctyl phthalate, distearyl phthalate, diisodecyl phthalate, dioctyl adipate, tricresyl phosphate, triphenyl phosphate, and the like.
Viscoelastic foams of the present invention can be prepared by combining viscoelastic foam formulations, a)-c), using Isocyanate index greater than 95%, along with any optional components i)-xii), with one or more catalysts and one or more blowing agents, or the individual components combined in the presence of one or more catalysts and one or more blowing agents, thereby producing viscoelastic foams that meet or exceed the requirements of BS5852. In some embodiments, the level of toluene di-amine present in the viscolelastic foam is less than 5 ppm, based on the total foam weight.
Blowing agents suitable for use herein include water, a volatile hydrocarbon, halocarbon, or halohydrocarbon, or mixtures of two or more such materials, preferably water. Catalysts suitable for use herein can be categorized as gel catalysts (e.g. stannous or tin salts), blow catalysts (e.g. amine catalysts), or “balanced” gel/blow catalysts. Gel catalysts promote the reaction between the reactive hydrogen atoms, particularly of the hydroxyl groups, and the isocyanates. Blow catalysts promote the reaction of the reactive hydrogen of water and the pluri-isocyanate. Non-limiting examples of suitable catalysts include amine catalysts, tin-based catalysts, bismuth-based catalysts or other organometallic catalysts, and the like. Examples of suitable tertiary amines as blowing catalyst include, e.g., bis(dimethylaminoethyl) ether and pentamethyldiethylentriamine. Examples of gel catalysts include 1,4-diaza(2,2,2)bicyclooctane; tetramethyldipropylentriamine; and tris(dimethylaminopropyl)hydrotriazine.
The above description is directed to several embodiments of the present invention. Those skilled in the art will recognize that other means, which are equally effective, could be devised for carrying out the spirit of this invention. It should also be noted that preferred embodiments of the present invention contemplate that all ranges discussed herein include ranges from any lower amount to any higher amount.
The following examples will illustrate the present invention, but are not meant to be limiting in any manner.
In the following examples, the components indicated in the examples were combined to form foams that were subjected to BS 5852 Crib 5 tests, and the results are reported in the examples. The components were combined under standard atmospheric conditions.
In the following examples, the components used were: Polyol 56 OH value: Caradol SC56-02, available from the Shell Chemicals Company; Polyol 200 OH value: Yukol 1030 available from SK Oxichemicals; Amine 2 catallyst: Dabco® 33 LV available from Air Products; Amine 1 catalyst: Dabco® A1 available from from Air Products or Niax A1 available from GE; Stannous Octoate: Dabco® T9 available from Air Products; and Silicone: Niax L 650 from GE or B 8229 from Degussa.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US08/71678 | 7/31/2008 | WO | 00 | 2/5/2010 |
| Number | Date | Country | |
|---|---|---|---|
| 60954500 | Aug 2007 | US |
