阅读说明：本技术 用于舒适应用的聚氨基甲酸酯泡沫 (Polyurethane foams for comfort applications ) 是由 Y·斯里瓦斯塔瓦 W·库恩斯 于 2018-12-13 设计创作，主要内容包括：通过使亲水性准预聚物、水和聚合物多元醇在硅酮表面活性剂和环氧乙烷/高碳环氧烷嵌段共聚物存在下反应来制得柔性聚氨基甲酸酯泡沫。所述泡沫合乎需要地展现低密度和压缩永久变形,并且具有良好的热特性和吸湿特性。所述泡沫适用于床上用品和其它“舒适”应用,其中所述泡沫暴露于体热且承载用户体重的至少一部分。所述热特性和吸湿特性有助于使用户感知到舒适。(Flexible polyurethane foams are made by reacting a hydrophilic quasi-prepolymer, water and a polymer polyol in the presence of a silicone surfactant and an ethylene oxide/homocarbosiloxane block copolymer. The foams desirably exhibit low density and compression set, and have good thermal and moisture absorption characteristics. The foam is suitable for bedding and other "comfort" applications in which the foam is exposed to body heat and bears at least a portion of the user's weight. The thermal and hygroscopic properties help to make the user feel comfortable.)

1. A flexible polyurethane foam comprising the reaction product of a reaction mixture comprising

a) An isocyanate functional quasi-prepolymer which is the reaction product of at least one hydroxyl terminated polymer of ethylene oxide and an excess of an organic polyisocyanate comprising at least 80% by weight of diphenylmethane diisocyanate wherein the diphenylmethane diisocyanate has at least 50% by weight of 4,4' -diphenylmethane diisocyanate, wherein the isocyanate functional quasi-prepolymer has an isocyanate content of from 5 to 15% by weight and contains from 30 to 70% by weight of ethylene oxide units, based on the weight of the isocyanate functional quasi-prepolymer,

b) the amount of water is controlled by the amount of water,

c) at least one polymer polyol comprising polymer particles dispersed in at least one base polyol,

d) at least one silicone surfactant, and

e) at least one ethylene oxide/homoalkylene oxide block copolymer, wherein

i) The quasi-prepolymer comprises 50 to 75% of the combined weight of components a-e;

ii) water comprises 15-41% of the combined weight of components a-e;

iii) said at least one polymer polyol comprises from 8 to 20% and said polymer particles comprise from 0.5 to 8% of the combined weight of components a-e;

iv) the at least one silicone surfactant comprises from 0.5 to 3% by combined weight of components a-e, and

v) the at least one ethylene oxide/homoalkylene oxide block copolymer comprises from 0.5 to 3 to 50 to 75 percent of the combined weight of components a-e.

2. The flexible polyurethane foam of claim 1, wherein the at least one polymer polyol comprises 9 to 15% of the combined weight of components a-e, and the polymer particles comprise 1.5 to 6% of the combined weight of components a-e.

3. A flexible polyurethane foam according to claim 1 or 2, wherein the polymer particles are particles of a copolymer of styrene and acrylonitrile.

4. The flexible polyurethane foam according to any one of the preceding claims, wherein the reaction mixture contains no more than 5 parts per million metal and no more than 100 parts per million amine compound by weight.

5. A flexible polyurethane foam according to any one of the preceding claims, wherein the silicone surfactant contains 25 to 70 wt% polysiloxane, 10 to 75 wt% polymerized ethylene oxide and 0 to 10 wt% polymerized propylene oxide, based on the weight of the silicone surfactant.

6. A flexible polyurethane foam according to any one of the preceding claims, wherein said ethylene oxide/homoalkylene oxide block copolymer contains from 40 to 90% ethylene oxide units and has a number average molecular weight of from 1,500 to 12,000.

7. A process for preparing a flexible polyurethane foam comprising

A. Forming a reaction mixture by mixing at least the following components a-e:

a) an isocyanate functional quasi-prepolymer which is the reaction product of at least one hydroxyl terminated polymer of ethylene oxide and an excess of an organic polyisocyanate comprising at least 80% by weight of diphenylmethane diisocyanate wherein the diphenylmethane diisocyanate has at least 50% by weight of 4,4' -diphenylmethane diisocyanate, wherein the isocyanate functional quasi-prepolymer has an isocyanate content of from 5 to 15% by weight and contains from 30 to 70% by weight of ethylene oxide units, based on the weight of the isocyanate functional quasi-prepolymer,

b) the amount of water is controlled by the amount of water,

c) at least one polymer polyol comprising polymer particles dispersed in at least one base polyol,

d) at least one silicone surfactant, and

e) at least one ethylene oxide/homoalkylene oxide block copolymer,

and

B. subjecting the reaction mixture formed in step A to conditions under which the isocyanate functional quasi-prepolymer and one or more of components b-e react to form the flexible polyurethane foam,

wherein the content of the first and second substances,

i) the quasi-prepolymer comprises 50 to 75% of the combined weight of components a-e;

ii) water comprises 15-41% of the combined weight of components a-e;

iii) said at least one polymer polyol comprises from 8 to 20% and said polymer particles comprise from 0.5 to 8% of the combined weight of components a-e;

iv) the at least one silicone surfactant comprises from 0.5 to 3% by combined weight of components a-e; and

v) the at least one ethylene oxide/homocarbosiloxane block copolymer comprises from 0.5 to 3% by weight of the combination of components a-e).

8. The method of claim 7, wherein the at least one polymer polyol comprises 9 to 15% and the polymer particles comprise 1.5 to 6% of the combined weight of components a-e.

9. The method of claim 7 or 8, wherein the polymer particles are particles of a copolymer of styrene and acrylonitrile.

10. The method of any one of claims 7-9, wherein the reaction mixture contains no more than 5 parts per million metal and no more than 100 parts per million amine compound by weight.

11. The method of any one of claims 7 to 10, wherein the silicone surfactant contains 25 to 70 weight percent polysiloxane, 10 to 75 weight percent polymerized ethylene oxide, and 0 to 10 weight percent polymerized propylene oxide, based on the weight of the silicone surfactant.

12. The method of any one of claims 7-11, wherein the ethylene oxide/homocarbosiloxane block copolymer contains 40 to 90% ethylene oxide units and has a number average molecular weight of 1,500 to 12,000.

13. The method of any one of claims 7-12, wherein the foam is dried to a constant weight after step B.

14. A cushion comprising the flexible polyurethane foam of any one of claims 1-6.

15. The cushion of claim 14, which is a pillow, mattress topper, mattress, comforter, furniture seat or back, automobile seat or back, bedding material, or an article of thermal clothing.

16. The cushion according to claim 14 or 15, wherein the flexible polyurethane foam has a density of 48 to 80kg/m when dried to a constant weight³And a compression set of 40% or less.

17. The cushion according to claim 14 or 15, wherein the flexible polyurethane foam has a density of 48 to 64kg/m when dried to a constant weight³And a compression set of 15% or less.

18. The cushion according to any one of claims 14 to 17, wherein the flexible polyurethane foam, when dried to constant weight, exhibits a specific heat of at least 1.5J/g ° K, a thermal conductivity of at least 0.05W/m ° K, a water absorption of 300% to 700%, and a moisture absorption time of 5 seconds or less, preferably 4 seconds or less.

Technical Field

The present invention relates to flexible polyurethane foams suitable for use in comfort applications such as pillows, mattresses, mattress toppers and seat cushions.

Background

Polyurethane foams are used in very large amounts to make cushioning materials, particularly for bedding and seating. A problem with these foams is that they do not conduct heat very efficiently. Thus, the heat released by the user is captured by the foam in the area immediately adjacent to the user's body. This results in a local temperature rise, which the user typically perceives as uncomfortable.

One way to address this problem is to make the foam more hydrophilic. The most commonly used polyurethane foams in these applications are to some extent hydrophobic materials that do not absorb too much moisture. The water vapour evaporated by the user is then captured in the vicinity of the user's body. This increases the local relative humidity and promotes local heat capture and discomfort for the person. The hydrophilic foam may absorb at least some of this water vapor and conduct it through the polymer mesh structure and out of the user. This dissipates heat and reduces the relative humidity adjacent the user's body, thereby improving perceived comfort.

Hydrophilic polyurethane foams for comfort applications are described in WO 2016/069437. The hydrophilic polyurethane foam is prepared by reacting 20 to 80 wt% of an aqueous component with correspondingly 80 to 20 wt% of a hydrophilic isocyanate-terminated prepolymer. The resulting foam has the benefits of high specific heat, high thermal conductivity, and high water absorption, all of which promote heat dissipation and comfort to a greater extent.

Disadvantageously, the density of the polyurethane foam examples of WO2016/069437 is higher than desired. The desired density is 5 pounds per cubic foot (80 kg/m)³) Or lower. In addition, low thermal conductivity is required.

Although lower densities can be achieved in various ways, lower density foams suffer from higher compression set than desired. Compression set is the permanent loss of foam height after compression of the foam. Higher compression set can cause sagging, formation of depressions, loss of foam height and shape, and other problems. Hydrophilic polyurethane foams are generally highly susceptible to higher compression set.

What is desired is a polyurethane foam suitable for comfort applications such as bedding and seat cushions. The foam should be able to dissipate heat and absorb moisture, but the foam density should be lower while also exhibiting lower compression set.

Disclosure of Invention

In one aspect, the present invention is a flexible polyurethane foam comprising the reaction product of a reaction mixture comprising

a) An isocyanate functional quasi-prepolymer which is the reaction product of at least one hydroxyl-terminated polymer of ethylene oxide and an excess of an organic polyisocyanate comprising at least 80% by weight of diphenylmethane diisocyanate, wherein the diphenylmethane diisocyanate has at least 50% by weight of 4,4' -diphenylmethane diisocyanate, wherein the isocyanate functional quasi-prepolymer has an isocyanate content of from 5 to 15% by weight and contains from 30 to 70% by weight of ethylene oxide units, based on the weight of the isocyanate functional quasi-prepolymer,

b) the amount of water is controlled by the amount of water,

c) at least one polymer polyol comprising polymer particles dispersed in at least one base polyol,

d) at least one silicone surfactant, and

e) at least one ethylene oxide/homoalkylene oxide block copolymer, wherein

i) The quasi-prepolymer comprises 50 to 75% of the combined weight of components a-e;

ii) water comprises 15-41% of the combined weight of components a-e;

iii) said at least one polymer polyol comprises from 8 to 20% and said polymer particles comprise from 0.5 to 8% of the combined weight of components a-e;

iv) the at least one silicone surfactant comprises from 0.5 to 3% by combined weight of components a-e, and

v) the at least one ethylene oxide/homocarbosiloxane block copolymer comprises from 0.5 to 3 percent by weight of the combination of components a-e.

The foams of the present invention have an excellent combination of properties including good heat and moisture conduction, low density and low compression set. This set of properties makes the foam particularly useful in bedding, seating and other "comfort" applications where the foam becomes exposed to body heat and/or to water vapor evaporating from the body of a human user. The foam or foam-containing article may support at least a portion of the weight of a human user in such applications.

The invention is also a process for preparing a flexible polyurethane foam comprising

A. Forming a reaction mixture by mixing at least the following components a-e:

a) an isocyanate functional quasi-prepolymer which is the reaction product of at least one hydroxyl-terminated polymer of ethylene oxide and an excess of an organic polyisocyanate comprising at least 80% by weight of diphenylmethane diisocyanate, wherein the diphenylmethane diisocyanate has at least 50% by weight of 4,4' -diphenylmethane diisocyanate, wherein the isocyanate functional quasi-prepolymer has an isocyanate content of from 5 to 15% by weight and contains from 30 to 70% by weight of ethylene oxide units, based on the weight of the isocyanate functional quasi-prepolymer,

b) the amount of water is controlled by the amount of water,

c) at least one polymer polyol comprising polymer particles dispersed in at least one base polyol,

d) at least one silicone surfactant, and

e) at least one ethylene oxide/homoalkylene oxide block copolymer,

and

B. subjecting the reaction mixture formed in step A to conditions under which the isocyanate functional quasi-prepolymer and one or more of components b-e react to form a flexible polyurethane foam,

wherein the content of the first and second substances,

i) the quasi-prepolymer comprises 50 to 75% of the combined weight of components a-e;

ii) water comprises 15-41% of the combined weight of components a-e;

iii) said at least one polymer polyol comprises from 8 to 20% and said polymer particles comprise from 0.5 to 8% of the combined weight of components a-e;

iv) the at least one silicone surfactant comprises from 0.5 to 3% by combined weight of components a-e; and

v) the at least one ethylene oxide/homocarbosiloxane block copolymer comprises from 0.5 to 3 percent by weight of the combination of components a-e.

Detailed Description

The quasi-prepolymer is the reaction product of an organic polyisocyanate comprising diphenylmethane diisocyanate (MDI) and a polyether containing oxyethylene groups. By "quasi-prepolymer" is meant that the reaction product is a mixture of free (unreacted) starting organic polyisocyanate and isocyanate-terminated prepolymer molecules formed in the reaction of the polyether and organic polyisocyanate molecules. The amount of free organic polyisocyanate may be, for example, at least 5%, at least 10%, at least 15% or at least 20% up to 50%, up to 35% or up to 30% or up to 25% of the total weight of the quasi-prepolymer.

In some embodiments, the number average isocyanate functionality of the organic polyisocyanate may be 1.95 to 2.15, preferably 1.95 to 2.05, and the isocyanate equivalent weight may be 123 to 128, preferably 124 to 126.

MDI represents at least 80% by weight of the organic polyisocyanate used to make the quasi-prepolymer. MDI may constitute at least 85%, at least 90% or at least 95% thereof, and may constitute up to 100% or up to 99% thereof. At least 50% by weight of the MDI is the 4,4' -isomer. In some embodiments, at least 60%, at least 70%, at least 75%, or at least 80% by weight of the MDI is the 4,4' -isomer. The 4,4' -isomer may constitute up to 100 wt.%, up to 99 wt.%, up to 98 wt.% of the MDI. The remainder of the MDI, if present, is made up of the 2, 4-isomer and/or the 2,2' -isomer. The 2,2' -isomer (if present) typically does not exceed 2% by weight of the MDI. The starting organic polyisocyanate used to make the quasi-prepolymer may contain up to 20 wt%, preferably up to 10 wt%, up to 5 wt% or up to 2 wt% of other isocyanate-containing compounds, but such other compounds may not be present. Such other organic polyisocyanates preferably have a molecular weight of 1000 or less, preferably 500 or less, and preferably contain 2 to 4 isocyanate groups per molecule. Examples of other organic isocyanates include polyphenylene polymethylene polyisocyanates having three or more rings, toluene diisocyanate, one or more aliphatic polyisocyanates, and the like, as well as isocyanate-containing compounds containing, for example, biuret, allophanate, urea, urethane, isocyanurate, and/or carbodiimide linkages.

The most preferred organic polyisocyanate used to make the quasi-prepolymer is an MDI product containing at least 60 wt.%, at least 70 wt.% or at least 80 wt.% 4,4'-MDI, up to 40 wt.%, preferably up to 30 wt.% or up to 20 wt.% 2,4' -MDI and 0 to 2 wt.% of other isocyanate compounds.

The polyethers used to prepare the quasi-prepolymers contain oxyethylene groups. It is preferably a hydroxyl-terminated homopolymer of ethylene oxide or a hydroxyl-terminated random or block copolymer of ethylene oxide and 1, 2-propylene oxide. The polyether may contain, for example, at least 50% by weight or at least 60% by weight of oxyethylene groups and up to 100% by weight of oxyethylene groups. Polyethers of particular interest are poly (ethylene oxide) homopolymers. The other is a random or block copolymer of ethylene oxide and 1, 2-propylene oxide containing from 50 to 95%, preferably from 60 to 95%, of oxyethylene groups and correspondingly from 5 to 50%, preferably from 5 to 40%, of 2-methyloxyethylene groups.

The polyether may nominally contain, for example, an average number of 2 to 4 hydroxyl groups per molecule. Preferred nominal average hydroxyl functionalities are from 2 to 3, and more preferred nominal average hydroxyl functionalities are from 2 to 2.5 or from 2 to 2.25. Nominal functionality refers to the number of oxyalkylatable groups on the initiator compound used to produce the polyether or polyethers. For the purposes of the present invention, a primary amino group is considered to contain 2 oxyalkylatable sites.

The equivalent weight of the polyether is preferably at least 300 or at least 450 and may for example be at most 6000, at most 3000 or at most 2000. An especially preferred equivalent weight range is 500 to 1800.

Mixtures of two or more polyethers as described above may be used to make the quasi-prepolymer.

When forming the quasi-prepolymer, a branching agent and/or chain extender is optionally present. Such branching or chain extending agents may have a hydroxyl equivalent weight of up to 250 or up to 125, and in the case of branching agents may have at least 3 hydroxyl groups per molecule, and in the case of chain extending agents may have exactly two hydroxyl groups per molecule. If these are present, they are advantageously present in an amount of at most 5, preferably at most 2, parts by weight per 100 parts by weight of polyether(s).

The equivalent weight and ethylene oxide content of the polyether(s) and the amount of organic polyisocyanate (and branching agent and chain extender (if present)) are selected together to produce a quasi-prepolymer having an isocyanate content of from 5 to 15% by weight of the quasi-prepolymer and an ethylene oxide content of from 30 to 75% by weight of the quasi-prepolymer. The isocyanate content may be at least 6% or at least 7%, and may be, for example, at most 12%, at most 10%, or at most 9%. The ethylene oxide content may be at least 40%, at least 50% or at least 55% and at most 70% or at most 65%.

The isocyanate content of the quasi-prepolymer can be determined using well known titration methods.

The ethylene oxide content of the quasi-prepolymer is preferably calculated from the ethylene oxide content of the polyether(s) and the weight of the reactive starting materials (i.e. the weight of the polyether(s) and organic polyisocyanate used to prepare the quasi-prepolymer) and the weight of any branching agent and/or chain extender that may be used.

The quasi-prepolymer is preferably prepared by mixing the starting organic polyisocyanate and the polyether(s) and subjecting the mixture to conditions under which a portion of the isocyanate groups react with the hydroxyl groups of the polyether(s) to form urethane linkages. The reaction is preferably carried out at elevated temperature (e.g., 60 to 180 ℃) and preferably under an inert atmosphere (e.g., nitrogen, helium, or argon). The reaction is generally continued until the prepolymer reaches a constant isocyanate content, which indicates that substantially all of the hydroxyl groups of the polyether have been consumed.

The quasi-prepolymer is preferably prepared in the substantial absence of a urethane catalyst (i.e., a catalyst for the reaction of isocyanate groups with hydroxyl groups to form urethanes). Specifically, the reaction mixture used to form the quasi-prepolymer preferably contains no more than 1 part per million by weight of metal and no more than 100 parts per million by weight of amine compound. The resulting quasi-prepolymer correspondingly contains similarly small amounts of such materials, if present. The one or more polyethers are preferably not amine initiated and do not additionally contain amine groups that exhibit activity as urethane catalysts.

The quasi-prepolymer is present in an amount of 50% to 75% by weight of the combination of components a-e. It may constitute at least 55% or at least 58% thereof, and may constitute at most 70% or at most 65% thereof.

Water comprises 15-41% of the combined weight of components a-e. Water may constitute at least 17%, at least 19% or at least 20% thereof, and may constitute at most 35% or at most 30% thereof.

The polymer polyol is a dispersion of a liquid base polyol containing polymer particles, the base polyol forming a continuous phase. Some or all of the polymer particles may be grafted to the base polyol. The polymer polyol may also include one or more stabilizers to which some or all of the polymer particles may be grafted.

The base polyol is one or more polyethers having a hydroxyl equivalent weight of at least 250. The hydroxyl equivalent weight can be at least 300, at least 350, at least 500, at least 800, at least 1000, or at least 1200, and can be, for example, at most 2500, at most 2000, or at most 1800. The base polyol may be a polymer or copolymer of propylene oxide. Homopolymers of propylene oxide and random and/or block copolymers of 50 to 99% by weight of propylene oxide and 1 to 50% of ethylene oxide are particularly suitable base polyols.

The nominal functionality of the base polyol may be from 2 to 6, especially from 2 to 4, and most preferably from 2 to 3. The "nominal functionality" of the base polyol refers to the average number of oxyalkylatable groups per molecule of the initiator compound or compounds used to make the base polyol. In some cases the actual functionality may be slightly lower than the nominal functionality.

A particularly preferred type of base polyol is prepared by homopolymerizing propylene oxide or randomly copolymerizing 75-99.9 weight percent propylene oxide and correspondingly 0.1 to 25 weight percent ethylene oxide onto a di-or trifunctional initiator, and optionally capping the resulting polyether with up to 30 weight percent (based on total product weight) ethylene oxide to form a base polyol having predominantly primary hydroxyl groups.

The dispersed polymer particles may comprise, for example, at least 1%, at least 5%, or at least 10% of the total weight of the polymer polyol, and may comprise, for example, up to 60%, up to 50%, up to 40%, up to 30%, or up to 20% of the total weight thereof.

In some embodiments, the dispersed polymer particles have a particle size of 100nm to 25 μm, more typically 250nm to 10 μm preferably at least 90% by volume of the dispersed polymer particles have a size within these ranges particle size is considered to be the diameter of a sphere of equivalent volume particle size measurements can be obtained by a laser diffraction method using equipment such as a Beckman-Coulter L X13320 laser diffraction particle size analyzer (Beckman-Coulter L X13320 laser diffraction particle size analyzer).

The dispersed polymer particles may be, for example, a polyurea, polyurethane and/or polyhydrazide or a polymer of one or more vinyl monomers. Suitable vinyl monomers include, for example, various polyolefins (e.g., polymers and copolymers of ethylene), various polyesters, various polyamides, various polycarbonates, various polymers and copolymers of acrylic and/or methacrylic acid esters, homopolymers or copolymers of styrene, homopolymers or copolymers of acrylonitrile, and the like. In some embodiments, the dispersed particles are styrene-acrylonitrile copolymer particles.

At least a portion of the dispersed polymer particles are preferably grafted to at least a portion of the base polyol molecules forming the continuous phase.

The dispersion of polyurea particles can be prepared by reacting a primary or secondary amine with a polyisocyanate in the presence of a base polyol. A process for producing polyurea dispersions is described, for example, in WO 2012/154831.

Dispersions of polyurethane particles can be prepared by reacting a low equivalent weight polyol or aminoalcohol with a polyisocyanate in the presence of a base polyol. Methods for producing such dispersions are described, for example, in US 4,305,857, WO 94/20558, WO 2012/154820.

Dispersions of polymerized vinyl monomers can be prepared by the in situ polymerization of such monomers in a base polyol. Such methods are described, for example, in USP 4,513,124, USP 4,588,830, USP 4,640,935 and USP 5,854,386. Alternatively, this type of dispersion may be formed in a melt-dispersion process, wherein a preformed vinyl polymer is melted and dispersed into the base polyol. This type of process is described in USP 6,613,827 and WO 2009/155427.

The one or more polymer polyols comprise at least 8% of the combined weight of components a-e. In some embodiments, the one or more polymer polyols comprise at least 9% thereof. The one or more polymer polyols comprise up to 20% and may comprise up to 18%, up to 15%, or up to 12% of the combined weight of components a-e.

The dispersed polymer particles comprise from 0.5% to 8% by combined weight of components a-e. The dispersed polymer particles may constitute at least 1%, at least 1.25% or at least 1.5% and at most 6%, at most 4%, at most 3% thereof.

The polymer polyol preferably contains no more than 5 parts per million or no more than 1 part per million metal and no more than 100 parts per million amine compound by weight. The base polyol or polyols are preferably not amine initiated and do not additionally contain amine groups that exhibit activity as urethane catalysts.

Suitable silicone surfactants are self-dispersible and/or water soluble. Among useful silicone surfactants are block copolymers having at least one polysiloxane block and at least one polyether block. Such block copolymers may be, for example, a-B or B-a-B type copolymers, wherein a represents a polysiloxane block and each B represents a polyether block. Such block copolymers may be of the pendant graft type structure, in which multiple polyether blocks are dependent on the polysiloxane block. Each polyether block is preferably a homopolymer or copolymer of ethylene oxide. The copolymer of ethylene oxide may be a copolymer of ethylene oxide and propylene oxide.

The silicone surfactant may contain, for example, 20 to 80 weight percent polysiloxane, 20 to 75 weight percent polymerized ethylene oxide, and 0 to 50 weight percent polymerized propylene oxide, based on the total weight of the silicone surfactant. More preferred silicone surfactants contain 20 to 80 weight percent polysiloxane, 20 to 75 weight percent polymerized ethylene oxide, and 0 to 20 weight percent polymerized propylene oxide. Even more preferred silicone surfactants contain 25 to 50 weight percent polysiloxane, 50 to 75 weight percent polymerized ethylene oxide, and 0 to 10 weight percent polymerized propylene oxide.

Suitable silicone surfactants are commercially available and include, for example, those available from Momentive (Momentive) toWater-soluble surfactants sold under the product name. This includes, for exampleL-7002, L-7200, L-7230, L-7600, L-7604, L-7605 and L7657 surfactants.

One or more silicone surfactants comprise 0.5 to 3% by combined weight of components a-e. The one or more silicone surfactants may comprise at least 0.75% or at least 1% thereof, and may comprise up to 2.5% or 2% thereof.

Block copolymers of ethylene oxide and homocarbocycloxanes contain one or more blocks of ethylene oxide and one or more blocks of polymerized homocarbocycloxanes. The homocyclic siloxane may be, for example, 1, 2-propylene oxide, 1, 2-butylene oxide, or mixtures thereof. Such block copolymers may contain, for example, 40 to 90 weight percent ethylene oxide units and have a number average molecular weight of 1500 to 12,000 (by gel permeation chromatography against polystyrene standards). Such block copolymers may have one or more hydroxyl groups, such as 1 to 4 hydroxyl groups or 2 to 4 hydroxyl groups. Examples of suitable block copolymers include Tergitol by The Dow Chemical Company^TMThose sold under the trade name Perkin (R), and Pluronics by BASF^TMThose sold under the trade name block copolymers.

The block copolymer of ethylene oxide and homocarbo siloxane preferably contains no more than 5 parts per million or no more than 1 part per million by weight of metal and no more than 100 parts per million of amine compound. It is preferably not initiated by an amine.

The reaction mixture may contain one or more optional ingredients in addition to components a-e as described above.

Among the suitable optional ingredients are one or more branching agents and/or chain extenders as previously described with respect to the preparation of quasi-prepolymers, but these may be omitted. If used, it is preferably present in an amount of up to 5 parts by weight or up to 2 parts by weight per 100 parts by weight of quasi-prepolymer.

Other suitable optional ingredients are additional isocyanate-reactive materials different from components a-e. If present, these preferably represent at most 5 parts by weight or at most 2 parts by weight per 100 parts by weight of quasi-prepolymer.

The reaction mixture may also contain various ingredients such as colorants, antioxidants, preservatives, biocides, fragrances, thickeners (such as xanthan gum (xanthan gum), various water-soluble cellulose ethers or polyacrylamides), mixing aids, wetting agents (when fillers are present), and the like. If present, these preferably represent up to 10% or up to 5% of the total weight of the reaction mixture.

Components a-e together preferably make up at least 90%, more preferably at least 95% or at least 98%, of the total weight of the reaction mixture, excluding any fillers.

The reaction mixture used for preparing the polyurethane foam is preferably substantially free of curing catalysts, i.e. catalysts for the reaction of isocyanate groups with water and/or alcohol groups. Specifically, the reaction mixture preferably contains no more than 5 parts per million, preferably no more than 1 part per million, of metal and no more than 100 parts per million of amine compound by weight.

In addition to components a to e, the reaction mixture may also contain one or more solid components, such as phase change agents, fillers and reinforcing materials. Examples of fillers include clays, diatomaceous earth, calcium carbonate, wollastonite, ground polymer particles, wood flour, cork flour, glass or other ceramic particles, and various types of natural and synthetic fibers, which may be woven, knitted or entangled as desired. Such solid components may constitute up to 75% of the total weight of the reaction mixture.

Polyurethane foams are prepared by combining the ingredients to form a reaction mixture and subjecting the resulting reaction mixture to conditions under which the isocyanate-functional quasi-prepolymer and one or more of components b-e react to form a flexible polyurethane foam.

The ingredients a-e may be combined in any order, but preferably the quasi-prepolymer is added or added simultaneously with the other ingredients to avoid premature reaction before the remaining ingredients can be added. Thus, for example, components b-e may be combined first, followed by addition of the quasi-prepolymer. Alternatively, components a-e may be combined all at once. It is also possible to form the components b to e in various sub-combinations, so that the sub-combinations are combined when the quasi-prepolymer is added. The optional isocyanate-reactive or water-soluble ingredients may be added with or separately from the water.

After mixing water with the quasi-prepolymer, curing occurs spontaneously, and thus a wide range of conditions is suitable for carrying out the reaction. The curing temperature may be as low as 0 ℃ or as high as, for example, 100 ℃. Temperatures close to room temperature or slightly elevated temperatures are well suited and generally preferred. Thus, the curing temperature may be at least 15 ℃ or at least 20 ℃ and at most 50 ℃,40 ℃ or 35 ℃. The curing reaction produces carbon dioxide gas, which forms cells and expands the reaction mixture as curing occurs.

The curing step may be carried out in an open container in which the expanding foam expands against the weight of the atmosphere and/or the weight of the film. Such free foaming process can be carried out by dispensing the reaction mixture into a tank where it foams and cures.

The curing step may instead be performed in a closed vessel (e.g., a closed mold) wherein expansion is constrained by the internal dimensions of the cavity to produce a foam having a size and shape corresponding to the size and shape of the mold cavity.

The amount of water in the reaction mixture is far in excess of the amount of isocyanate groups of the quasi-prepolymer. Because of this, cured foams typically contain a substantial amount of moisture, which may be at least partially in the form of the liquid contained in the cells of the foam. A drying step may be performed to remove some or all of this excess water.

Such a drying step may be performed, for example, by passing a drying gas through the foam, by leaving the foam to stand under a dry atmosphere, and/or by heating the foam to a temperature of, for example, 50 to 150 ℃. Drying may be carried out until any desired moisture content is achieved. In some embodiments, drying is performed until a constant foam weight is reached, indicating that all residual water is removed from the foam.

The foam density of the foams of the present invention may be, for example, from 40 to 144kg/m as measured according to ASTM D3574³. The invention has the obvious advantage that 80kg/m is easy to obtain³And lower foam density. In some embodiments, the foam density is from 48 to 80kg/m³Or 48 to 64kg/m³。

The foam of the present invention exhibits low compression set when dry in addition to low foam density.compression set is measured on a 5 × 5 × 2.54.54 cm skinless sample according to ASTM D-3774: D.thickness of the sample is measured with a micrometer.the sample is then placed between steel plates, its original thickness is compressed by 90% and aged at 70 ℃ under compression for 22 hours.the sample is then removed from the test equipment and allowed to recover at room temperature for 30 minutes before re-measuring its thickness the compression set is calculated as [ 100% × (original thickness-final thickness) ]/"original thickness.

When dried to constant weight as described above, the foams of the present invention can exhibit a specific heat of at least 1.5J/g.DEG.K (measured as described in WO 2016/069437). The specific heat can be at least 2J/g.DEG K, at least 2.1J/g.DEG K, at least 2.2J/g.DEG K, at least 2.5J/g.DEG K, or at least 2.7J/g.DEG K.

When dried to constant weight as described above, the foams of the present invention can exhibit a thermal conductivity of at least 0.03W/m ° K (measured as described in WO 2016/069437). The thermal conductivity can be at least 0.04W/m.DEG K, and can be, for example, 0.2W/m.DEG K or at most 0.1W/m.DEG K.

The inventive foam may exhibit a water absorption of 300% to 700% the water absorption is measured on a 5 × 5 × 2.54.54 cm skinless sample dried to constant weight and weighed.

In some embodiments, the foam exhibits a moisture absorption time of 5 seconds or less, preferably 4 seconds or less, the moisture absorption time is measured on a 5 × 5 × 2.54.54 cm skinless sample dried to constant weight, 3m L room temperature water is slowly dropped from a pipette onto the top surface of the foam sample, and the amount of time required for the foam to absorb water is recorded as the wicking time.

The ability of the foam to dissipate heat is sometimes indicated by comparing the surface temperature of the foam to the temperature of the surrounding air. After exposure to constant temperature air for a sufficient time to allow the foam to reach thermal equilibrium (e.g., for 24 hours), good heat dissipation may be indicated by the foam having a lower surface temperature than the surrounding air. When conditioned at room temperature for 24 hours, the surface temperature may be, for example, 0.1 to 3 ℃ lower than the ambient air. Preferably, the surface temperature is measured with an infrared thermometer.

The foams of the present invention are suitable for use in bedding, seating and other "comfort" applications. Comfort applications include those in which the foam becomes exposed to body heat or to water vapor evaporating from the body of a human user during use. In such applications the foam or foam-containing article typically supports at least a portion of the weight of a human user and is compressed during use. Examples of such comfort applications include pillows; mattress toppers, mattresses, comforters, furniture and/or car seats; bedding material; taken with heat insulation, etc.

The following examples are provided to illustrate the invention, but are not intended to limit its scope. All parts and percentages are by weight unless otherwise indicated.

Examples 1-2 and comparative samples A-F

A. Quasi-prepolymer formation

Quasi-prepolymers A-C were prepared in the following general manner from the ingredients as indicated in Table 1. The polyol or polyols were dried to a moisture content of less than 250ppm by heating the polyol to 100 ℃ overnight with stirring under nitrogen. A trace amount of benzoyl chloride was added to the dry polyol and stirred. Separately, the polyisocyanate(s) are heated to 50 ℃ and combined with the polyol(s). A urethane catalyst is not added to the resulting reaction mixture, which contains no more than 1 part per million by weight of metal and no more than 100 parts per million by weight of amine compound. The reaction mixture was heated at 75 ℃ under nitrogen until a constant isocyanate content was obtained. The quasi-prepolymer was then cooled to room temperature and stored under nitrogen.

NCO content was measured according to ASTM D5155. The ethylene oxide content of the quasi-prepolymer is calculated from the ethylene oxide content of the starting materials. The 4,4 '-content of the starting polyisocyanate is calculated from the 4,4' -content of the starting isocyanate. The values obtained are reported in table 1.

Polyol a is a 1000 molecular weight nominal difunctional homopolymer of ethylene oxide. It contains 100% oxyethylene groups. Polyol A can be used as Carbowax^TM1000 polyol is commercially available from the Dow chemical company.

Polyol B is a copolymer of ethylene oxide and propylene oxide having a nominal hydroxyl functionality of 2 and a number average molecular weight of about 2,400 g/mol. It contains 64% oxyethylene groups. Polyol B can be used as UCON^TMPC L-270 polyol is commercially available from the Dow chemical company.

Polyol C is a copolymer of ethylene oxide and propylene oxide having a nominal hydroxyl functionality of 3 and a number average molecular weight of about 5,000g/mol, which contains 75% oxyethylene groups polyol C can be referred to as VORANO L^TMCP-1421 polyol is commercially available from the Dow chemical company.

Polyol D is a homopolymer of propylene oxide. It has a nominal hydroxyl functionality of 2 and a number average molecular weight of about 2000 g/mol.

Isocyanate A is a mixture of 98% 4,4'-MDI and 2% 2,4' -MDI. It has an isocyanate content of 33.5%. Isocyanate A can be used as ISONATE^TM125M polyisocyanate is commercially available from the Dow chemical company.

Isocyanate B is a mixture of 50% 4,4'-MDI and 50% 2,4' -MDI. It has an isocyanate content of 33.5%. Isocyanate B can be used as ISONATE^TM50O, P polyisocyanate is commercially available from the Dow chemical company.

TABLE 1

B. Preparation of polyurethane foams

Polyurethane foams are prepared by separately reacting the aforementioned quasi-prepolymers with an aqueous phase. The aqueous phase contained the ingredients as set forth in table 2. In each case, the various constituents of the aqueous phase were first combined and the resulting aqueous phase was mixed with the quasi-prepolymer at room temperature in a high-speed laboratory mixer. The reaction mixture was poured into an open mold and allowed to foam and cure without the application of heat.

The silicone surfactant is a silicone/ethylene oxide block copolymer containing about 70% by weight polymerized ethylene oxide. Which is composed of a chart andl-7605.

The ethylene oxide/propylene oxide block copolymer was a triblock copolymer having 1750g/mol of an internal poly (propylene oxide) block and the internal poly (propylene oxide) block contained 80 weight percent of a terminal poly (ethylene oxide) block. Its nominal functionality is 2 hydroxyl groups per molecule.

The polymer polyol is a 20% by weight styrene-acrylonitrile particle dispersion in a base polyol. The base polyol is a block copolymer of propylene oxide and ethylene oxide having an average hydroxyl number of about 36, a nominal functionality of 3 and containing 20 weight percent ethylene oxide units. The particle size is generally between 300nm and 10 μm.

TABLE 2

^*Comparison

After curing, the foam was cured overnight at ambient conditions. The skin was removed and the foam was aged for 24 hours at ambient conditions prior to testing. The foam was evaluated for density and air flow rate according to ASTM D3574. Other samples (except comparative sample a) were dried to constant weight and compression set, moisture absorption, thermal conductivity, and specific heat were described above according to the test methods. The results are shown in table 3.

TABLE 3

^*Comparison was measured on undried foam samples.

Comparative sample a corresponds to example 1 of WO 2016/069537. This foam was made without polymer polyol and using silicone surfactant instead of ethylene oxide/propylene block copolymer. The foam has good properties overall, but about 109kg/m³Is higher than desired.

Comparative sample B demonstrates the effect of introducing a copolymer polyol into an aqueous phase containing a silicone surfactant but no ethylene oxide/propylene oxide block copolymer. These adjustments allow a reduction in density to about 75kg @³But a compression set higher than 47%.

In comparative sample C, the silicone surfactant of comparative sample B was replaced with an ethylene oxide/propylene oxide block copolymer. Foam density, air flow rate and compression set all have significant effects.

Example 2 is the same as comparative sample B and comparative sample C, except that both the silicone surfactant and the ethylene oxide/propylene oxide block copolymer are present in the aqueous phase. The density is reduced to less than 60kg/m³And compressThe permanent set is significantly reduced to 10%. At the same time, good moisture absorption is maintained and a higher air flow rate is obtained.

Example 1 demonstrates the effect of using a quasi-prepolymer with a slightly lower ethylene oxide content. The density was significantly lower than any of comparative samples a-C and the compression set was significantly reduced. Moisture absorption is retained. Example 1 represents a significant improvement over the comparative samples a-C.

Comparative sample D and comparative sample E demonstrate the effect of varying the amount of polymer polyol. Too little polymer polyol (D) or too much polymer polyol (E) results in a significant and undesirable increase in compression set. Too little polymer polyol also results in a significant increase in density.

Comparative sample F shows that a quasi-prepolymer containing oxyethylene groups is required. Quasi-prepolymers are not even capable of forming stable foams without the hydrophilic nature imparted by the oxyethylene groups.