Patent Application
20210130562
This invention relates to polyurethane foams that exhibit reduced levels of formaldehyde and acetaldehyde emissions, and to methods for producing such polyurethane foams.
Emissions from polymeric materials are a concern in many applications, especially when people or animals are exposed to the polymeric material within an enclosed space. Materials used in workspace, home and vehicular environments are a particular concern. Vehicle manufacturers are imposing stricter limits on the emissions from polymeric materials that are used in the passenger cabins of cars, trucks trains and aircraft. Aldehyde emissions, especially formaldehyde and acetaldehyde, are a particular cause of concern.
Polyurethane foams are used in many office, household and vehicular applications. They are used, for example, in appliance applications and as cushioning for bedding and furniture. In automobiles and trucks, polyurethanes are used as seat cushioning, in headrests, in dashboards and instrument panels, in armrests, in headliners, and other applications. These polyurethanes often emit varying levels of formaldehyde and acetaldehyde.
Scavengers are sometimes used to reduce aldehyde emissions from various types of materials. In the polyurethane field, there is, for example, WO 2006/111492, which describes adding antioxidants and hindered amine light stabilizers (HALS) to polyols to reduce aldehydes. WO 2009/114329 describes treating polyols with certain types of aminoalcohols and treating polyisocyanates with certain nitroalkanes, in order to reduce aldehydes in the polyols and polyisocyanates, respectively, and in polyurethanes made from those materials. JP 2005-154599 describes the addition of an alkali metal borohydride to a polyurethane formulation for that purpose. U.S. Pat. No. 5,506,329 describes the use of certain aldimine oxazolidine compounds for scavenging formaldehyde from polyisocyanate-containing preparations, and describes nitroalkanes and aminoalcohols as formaldehyde scavengers in textile and plywood applications.
These approaches provide limited benefit, in part because aldehydes present in polyurethane foam are not always carried in from the raw materials used to make the foam. Formaldehyde and acetaldehyde in particular can form during the curing step or when the foam is later subjected to UV light, elevated temperatures or other conditions. Because of the cellular structure of these foams, aldehydes generated in this way often can escape easily into the atmosphere and so can present an exposure concern. Therefore, simply treating the starting materials is not always an adequate solution to the emission of aldehydes from polyurethane foams.
Another problem is that measures that are effective against formaldehyde emissions are not always effective against acetaldehyde emissions, and vice versa. For example, applicants have found that whereas the antioxidants described in WO 2006/111,492 are effective in reducing acetaldehyde emissions, they can actually cause an increase in formaldehyde emissions. Applicants have further found that the presence of HALS often leads to an increase in formaldehyde emissions, acetaldehyde emissions or both. Nonetheless, it is often desirable to include HALS materials in the foam formulation to provide for light stability (apart from any impact on aldehyde emissions). Therefore, a method for overcoming the negative effects of antioxidants and HALS materials on formaldehyde emissions, while preserving their desired benefits of acetaldehyde reduction and light stability, is wanted.
In other arenas, U.S. Pat. No. 6,646,034 and US Publication No. 2011-0034610 describe adding various formaldehyde scavengers, such as organic compounds having amino or imino groups, including certain aminoalcohol compounds and acetoacetamide, to a polyacetal resin. US Publication No. 2010-0124524 describes a method for scavenging airborne formaldehyde with certain amine-functional scavengers. USP 5,599,884 describes removing formaldehyde from amino resins using acetoacetamide, among other materials.
An inexpensive and effective method to reduce both formaldehyde and acetaldehyde emissions from polyurethane foams is highly desired. Preferably, this method does not result in a significant change in the properties or performance of the polyurethane.
This invention is a method for producing a polyurethane foam comprising forming a reaction mixture that contains an aromatic polyisocyanate, at least one isocyanate-reactive material having an average functionality of at least 2 and an equivalent weight of at least 200 per isocyanate-reactive group, at least one blowing agent, at least one surfactant and at least one catalyst, and curing the reaction mixture to form the foam in the presence of:
(i) at least one aminoalcohol, preferably having the structure:
The invention is also a process for reducing formaldehyde and acetaldehyde emissions from a polyurethane foam, comprising: a) mixing a aminoalcohol compound (i) and at least one antioxidant (ii) with at least one isocyanate-reactive material having an average functionality of at least 2 and an equivalent weight of at least 200 per isocyanate-reactive group and then b) combining the mixture from step a) with at least one organic polyisocyanate and curing the resulting combination in the presence of at least one blowing agent, at least one surfactant, at least one catalyst and at least one antioxidant to form a polyurethane foam.
The invention is also a polyurethane foam made in either of the foregoing processes.
The invention provides an inexpensive and practical method by which one can produce polyurethane foams that emit very low levels of both formaldehyde and acetaldehyde, preferably a polyurethane foam of which exhibits formaldehyde and acetaldehyde emissions each no greater than 1 μg/100 mm by 80 mm by 50 mm test piece.
Aminoalcohol compounds are known, for example, see US Publication Nos. 2009/0227758 and 2010/0124524, all of which are incorporated herein in their entirety.
In one embodiment (referred to as embodimentl), suitable aminoalcohol compounds (i) include those having the structure:
or salt thereof, wherein
RA is a bond or is C(R7R8);
R1 is H, OH or C1-C6 alkyl;
R2 is H, OH or C1-C6 alkyl;
R3, R4, R5, and R6 are independently H, or C1-C6 alkyl;
R7 and R8 are independently H, OH or C1-C6 alkyl;
wherein alkyl in R1-R8 is optionally independently substituted with OH, NR9R19, C1-C6 alkyl, or phenyl, wherein R9 and R19 are independently H or C1-C6 alkyl,
and
provided that if neither R7 nor R8 is OH, then at least one of R1 and R2 is OH.
Preferably in embodiment 1, R1 is H (embodiment 2).
Preferably in embodiments 1 and 2, RA is a bond and R2 is OH (embodiment 3). Further preferably in this embodiment, R1, R3, and R4 are each H, R5 is H or optionally substituted C1-C6 alkyl, and R6 is optionally substituted C1-C6 alkyl, preferably C1-C3 alkyl, more preferably methyl.
Preferably in embodiments 1-3, R1, R3, and R4 are each H and R5 and R6 are independently optionally substituted C1-C6 alkyl, more preferably one of R5 and R6 is unsubstituted and the other is substituted with OH.
Preferably in embodiments 1-3, R1, R3, and R4 are each H and R5 and R6 are independently optionally substituted C1-C6 alkyl, more preferably both of R5 and R6 are substituted with OH.
Preferably in embodiment 1, R1 is OH (embodiment 4). More preferably within this embodiment, RA is a bond and R2, R3, R4, and R5 are each H, and R6 is optionally substituted C1-C6 alkyl, preferably unsubstituted C1-C3 alkyl, more preferably methyl.
Particularly preferred aminoalcohols according to embodiments 1-4 are 2-amino-1-butanol, 2-amino-2-ethyl-1,3-propanediol, 2-amino-2-methyl-1-propanol, 2-amino-1-methyl-1,3-propanediol, 2-amino-2(hydroxymethyl)propane-1,3-diol or tris (hydroxymethyl) aminomethane, N-isopropylhydroxylamine, ethanolamine, diethanolamine, N-methylethanolamine, N-butylethanolamine, monoisopropanolamine, diisopropanolamine, mono-sec-butanolamine, di-sec-butanolamine, and salts thereof. An especially preferred formaldehyde scavenger is tris (hydroxymethyl) aminomethane. These aminoalcohols are available from a variety of commercial sources, including ANGUS Chemical Company (Buffalo Grove, Ill., USA), The Dow Chemical Company (Midland, Mich., USA), or can be readily prepared by techniques well known in the art. The formula I compounds can be used in the form of salts. Suitable salts include hydrochloride, acetate, formate, oxalate, citrate, carbonate, sulfate, and phosphate.
The process of the invention is performed in the presence of at least one antioxidant (ii). Examples of suitable antioxidants include, for example:
1) Phenolic compounds such as 2,6-di-tert-butyl-4-methylphenol, 2-tert-butyl-4,6-dimethylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-n-butylphenol, 2,6-di-test-butyl-4-isobutylphenol, 2,6-dicyclopentyl-4-methylphenol, 2-(a-methylcyclohexyl)-4,6-dimethylphenol, 2,6-dioctadecyl-4-methylphenol, 2,4,6-tricyclohexylphenol, 2,6-di-tert-butyl-4-methoxymethylphenol, nonylphenols which are linear or branched in the side chains, for example 2,6-di-nonyl-4-methylphenol, 2,4-dimethyl-6-(1′-methylundec-1′-yl)phenol, 2,4-dimethyl-6-(1′-methylheptadec-1′-yl)phenol, 2,4-dimethyl-6-(1′-methyltridec-1′-yl)phenol, 2,4-dioctylthiomethyl-6-tert-butylphenol, 2,4-dioctylthiomethyl-6-methylphenol, 2,4-dioctylthiomethyl-6-ethylphenol, 2,6-di-dodecylthiomethyl-4-nonylphenol, 2,6-di-tert-butyl-4-methoxyphenol, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylhydroquinone, 2,6-diphenyl-4-octadecyloxyphenol, 2,6-di-tert-butylhydroquinone, 2,5-di-tert-butyl-4-hydroxyanisole, 3,5-di-tert-butyl-4-hydroxyanisole, 3,5-di-tert-butyl-4-hydroxyphenyl stearate, bis(3,5-di-tert-butyl-4-hydroxyphenyl) adipate, 2,2′-methylenebis(6-tert-butyl-4-methylphenol), 2,2′-methylenebis(6-tert-butyl-4-ethylphenol), 2,2′-methylenebis[4-methyl-6-(α-methylcyclohexyl)phenol], 2,2′-methylenebis(4-methyl-6-cyclohexylphenol), 2,2′-methylenebis(6-nonyl-4-methylphenol), 2,2′-methylenebis(4,6-di-tert-butylphenol), 2,2′-ethylidenebis(4,6-di-tert-butylphenol), 2,2′-ethylidenebis(6-tert-butyl-4-isobutylphenol), 2,2′-methylenebis[6-(α-methylbenzyl)-4-nonylphenol], 2,2′-methylenebis[6-(α,α-dimethylbenzyl)-4-nonylphenol], 4,4′-methylenebis(2,6-di-tert-butylphenol), 4,4′-methylenebis(6-tert-butyl-2-methylphenol), 1,1-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butane, 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-methylphenol, 1,1,3-tris(5-tert-butyl-4-hydroxy-2-methylphenyl)butane, 1,1-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)-3-n-dodecylmercaptobutane, ethylene glycol bis[3,3-bis(3′-tert-butyl-4′-hydroxyphenyl)butyrate], bis(3-tert-butyl-4-hydroxy-5-methyl-phenyl)dicyclopentadiene, bis[2-(3′-tert-butyl-2′-hydroxy-5′-methylbenzyl)-6-tert-butyl-4-methylphenyl]terephthalate, 1,1-bis-(3,5-dimethyl-2-hydroxyphenyl)butane, 2,2-bis(3,5-di-tert-butyl-4-hydroxyphenyl)propane, 2,2-bis-(5-tert-butyl-4-hydroxy2-methylphenyl)-4-n-dodecylmercaptobutane, 1,1,5,5-tetra(5-tert-butyl-4-hydroxy-2-methylphenyl)pentane, 1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene, 1,4-bis(3,5-di-tert-butyl-4-hydroxybenzyl)-2,3,5,6-tetramethylbenzene, 2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)phenol, esters of 13-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid with mono- or polyhydric alcohols, e.g. with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1,6-hexanediol, 1,9-nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N′-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hydroxymethyl-1-phospha-2,6,7-trioxabicyclo[2.2.2]octane, esters of β-(5-tert-butyl-4-hydroxy-3-methylphenyl)propionic acid with mono- or polyhydric alcohols, e.g. with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1,6-hexanediol, 1,9-nonanediol, ethylene glycol, 2 0 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N′-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hydroxymethyl-1-phospha-2,6,7-trioxabicyclo[2.2.2]octane; 3,9-bis [2-{3-(3 -tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy}-1,1-dimethylethyl]-2,4,8,10-tetraoxaspiro[5.5]-undecane, esters of β-(3,5-dicyclohexyl-4-hydroxyphenyl)propionic acid with mono- or polyhydric alcohols, e.g. with methanol, ethanol, octanol, octadecanol, 1,6-hexanediol, 1,9-nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N′-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hydroxymethyl-l-phospha-2,6,7-trioxabicyclo[2.2.2]octane, esters of 3,5-di-tert-butyl-4-hydroxyphenyl acetic acid with mono- or polyhydric alcohols, e.g. with methanol, ethanol, octanol, octadecanol, 1,6-hexanediol, 1,9-nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N′-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, and 4-hydroxymethyl-l-phospha-2,6,7-trioxabicyclo[2.2.2]octane. 2) Aminic antioxidants such as N,N′-di-isopropyl-p-phenylenediamine, N,N′-di-sec-butyl-p-phenylenediamine, N,N′-bis(1,4-dimethylpentyl)-p-phenylenediamine, N,N′-bis(1-ethyl-3methylpentyl)-p-phenylenediamine, N,N′-bis(1-methylheptyl)-p-phenylenediamine, N,N′-dicyclohexyl-p-phenylenediamine, N,N′-diphenyl-p-phenylenediamine, N,N′-bis(2-naphthyl)-p-phenylenediamine, N-isopropyl-N′-phenyl-p-phenylenediamine, N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine, N-(1-methylheptyl)-N′-phenyl-p-phenylenediamine, N-cyclohexyl-N′-phenyl-p-phenylenediamine, 4-(p-toluenesulfamoyl)diphenylamine, N,N′-dimethyl-N,N′-di-sec-butyl-p-phenylenediamine, diphenylamine, N-allyldiphenylamine, 4-isopropoxydiphenylamine, N-phenyl-1-naphthylamine, N-(4-tert-octylphenyl)-1-naphthylamine, N-phenyl-2-naphthylamine, octylated diphenylamine, for example p,p′-di-tert-octyldiphenylamine, 4-n-butyl-aminophenol, 4-butyrylaminophenol, 4-nonanoylaminophenol, 4-dodecanoylaminophenol, 4-octadecanoylaminophenol, bis(4-methoxyphenyl)amine, 2,6-di-tert-butyl-4-dimethylaminomethylphenol, 2,4′-diaminodiphenylmethane, 4,4′-diaminodiphenylmethane, N,N,N′,N′-tetra-methyl-4,4′-diaminodiphenylmethane, 1,2-bis[(2-methylphenyl)aminolethane, 1,2-bis(phenylamino)propane, (o-tolyl)biguanide, bis14-(1′,3′-dimethylbutyl)phenyl]amine, tert-octylated N-phenyl-1-naphthylamine, a mixture of mono- and dialkylated tert-butyl/tert-octyldiphenylamines, a mixture of mono- and dialkylated nonyldiphenylamines, a mixture of mono- and dialkylated dodecyldiphenylamines, a mixture of mono- and dialkylated isopropyl/isohexyldiphenylamines, a mixture of mono- and dialkylated tert-butyldiphenylamines, and the like.
3) Thiosynergists such as dilauryl thiodipropionate or distearyl thiodipropionate.
4) Phosphites and phosphonites such as triphenyl phosphite, diphenylalkyl phosphites, phenyldialkyl phosphites, tris(nonylphenyl) phosphite, trilauryl phosphite, trioctadecyl phosphite, distearylpentaerythritol diphosphite, tris(2,4-di-tert-butylphenyl) phosphite, diisodecyl pentaerythritol diphosphite, bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite, bis(2,4-di-cumylphenyl)pentaerythritol diphosphite, bis(2,6-di-tert-butyl-4-methylphenyl)pentaerythritol diphosphite, diisodecyloxypentaerythritol diphosphite, bis(2,4-di-tert-butyl-6-methylphenyl)pentaerythritol diphosphite, bis(2,4,6-tris(tert-butylphenyl)pentaerythritol diphosphite, tristearyl sorbitol triphosphite, tetrakis(2,4-di-tert-butylphenyl) 4,4′-biphenylene diphosphonite, 6-isooctyloxy-2,4,8,10-tetra-tert-butyl-12H-dibenz[d,g]-1,3,2-dioxaphosphocin, bis(2,4-di-tert-butyl-6-methylphenyl)methyl phosphite, bis(2,4-di-tert-butyl-6-methylphenyl)ethyl phosphite, 6-fluoro-2,4,8,10-tetra-tert-butyl-12-methyl-dibenz[d,g]-1,3,2-dioxaphosphocin, 2,2′,2″-nitrilo-[triethyltris(3,3′,5,5′-tetra-tert-butyl-1,1′-biphenyl-2,2′-diyl)phosphite], 2-ethylhexyl(3,3′,5,5′-tetra-tert-butyl-1,1′-biphenyl-2,2′-diyl)phosphite, and 5-butyl-5-ethyl-2-(2,4,6-tri-tert-butylphenoxy)-1,3,2-dioxaphosphirane.
5) Benzofuranones and indolinones such as those disclosed in U.S. Pat. No. 4,325,863; U.S. Pat. No. 4,338,244; U.S. Pat. No. 5,175,312; U.S. Pat. No. 5,216,052; U.S. Pat. No. 5,252,643; DE-A-4316611; DE-A-4316622; DE-A-4316876; EP-A-0589839 or EP-A-0591102, including for example 3-[4-(2-acetoxyethoxy)phenyl]-5,7-di-tert-butylbenzofuran-2-one, 5,7-di-tert-butyl-3-(4-(2-stearoyloxyethoxy)phenyl)benzofuran-2-one, 3,3′-bis[5,7-di-tert-butyl-3-(4-[2-hydroxyethoxylphenyl)benzofuran-2-one], 5,7-di-tert-butyl-3-(4-ethoxyphenyl)benzofuran-2-one, 3-(4-acetoxy-3,5-dimethylphenyl)-5,7-di-tert-butylbenzofuran-2-one, dimethyl-4-pivaloyloxyphenyl)-5,7-di-tert-butylbenzofuran-2-one, 3-(3,4-dimethylphenyl)-5,7-di-tert-butylbenzofuran-2-one, 3-(2,3-dimethylphenyl)-5,7-di-tert-burylbenzofuran-2-one, as well as
6) tocophenols, hydroxylated thiodiphenyl ethers, O-, N- and S-benzyl compounds, hydroxybenzylated malonates, triazine compounds, benzylphosphonates, acylaminophenols, amides of β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid, ascorbic acid (vitamin C), 2-(2′-hydroxyphenyl)benzotriazoles, 2-hydroxybenzophenones, esters of substituted and unsubstituted benzoic acids, acrylates, nickel compounds, oxamides, 2-(2-hydroxyphenyl)-1,3,5-triazines, hydroxylamines, nitrones, and esters of β-thiodipropionic acid, as described, for example, in U.S. Pat. No. 6,881,774, incorporated herein by reference.
Preferred antioxidants include:
In some embodiments, a HALS (hindered amine light stabilizer) compound is present. The HALS compound can be used, for example, in conjunction with an antioxidant as described in any of 1)-5) above, or in conjunction with any of mixtures a)-h) above. Suitable HALS compounds include bis(1-octyloxy)-2,2,5,5-tetramethyl-4-piperidinyl) sebacate (TINUVIN™ 123 from BASF), n-butyl-(3,5-di-tert-butyl-4-hydroxylbenzyl)bis-(1,2,2,6-pentamethyl-4-piperidinyl)malonate (TINUVIN 144 from BASF), dimethyl succinate polymer with 4-hydroxy-2-2,6,6-tetramethyl-l-piperidinethanol (TINUVIN 622 from BASF), bis(1,2,2,6,6-pentamethyl-4-piperidinyl) sebacate (TINUVIN 765 from BASF) and bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate (TINUVIN 770 from BASF) and the like.
To produce the foam, at least one polyisocyanate is reacted with at least one isocyanate-reactive compound that has a functionality of at least 2 and an equivalent weight of at least 200 per isocyanate-reactive group. “Functionality” refers to the average amount of isocyanate-reactive groups per molecule; the functionality may be as much as 8 or more but preferably is from 2 to 4. The isocyanate groups may be, for example, hydroxyl, primary amino or secondary amino groups, but hydroxyl groups are preferred. The equivalent weight may be up to 6000 or more, but is preferably from 500 to 3000 and more preferably from 1000 to 2000. This isocyanate-reactive compound may be, for example, a polyether polyol, a polyester polyol, a hydroxyl-terminated butadiene polymer or copolymer, a hydroxyl-containing acrylate polymer, and the like. A preferred type of isocyanate-reactive compound is a polyether polyol, especially a polymer of propylene oxide or a copolymer of propylene oxide and ethylene oxide. A copolymer of propylene oxide and ethylene oxide may be a block copolymer having terminal poly(oxyethylene) blocks and at least 50% primary hydroxyl groups. Another suitable copolymer of propylene oxide and ethylene oxide may be a random or pseudo-random copolymer, which may also contain terminal poly(oxyethylene) blocks and at least 50% primary hydroxyl groups.
Polyester polyols that are useful as the isocyanate-reactive compound include reaction products of polyols, preferably diols, with polycarboxylic acids or their anhydrides, preferably dicarboxylic acids or dicarboxylic acid anhydrides. The polycarboxylic acids or anhydrides may be aliphatic, cycloaliphatic, aromatic and/or heterocyclic and may be substituted, such as with halogen atoms. The polycarboxylic acids may be unsaturated. Examples of these polycarboxylic acids include succinic acid, adipic acid, terephthalic acid, isophthalic acid, trimellitic anhydride, phthalic anhydride, maleic acid, maleic acid anhydride and fumaric acid. The polyols used in making the polyester polyols preferably have an equivalent weight of about 150 or less and include ethylene glycol, 1,2- and 1,3-propylene glycol, 1,4- and 2,3-butane diol, 1,6-hexane diol, 1,8-octane diol, neopentyl glycol, cyclohexane dimethanol, 2-methyl-1,3-propane diol, glycerine, trimethylol propane, 1,2,6-hexane triol, 1,2,4-butane triol, trimethylolethane, pentaerythritol, quinitol, mannitol, sorbitol, methyl glycoside, diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol, dibutylene glycol and the like. Polycaprolactone polyols such as those sold by The Dow Chemical Company under the trade name “Tone” are also useful.
Mixtures of two or more isocyanate-reactive compounds having a functionality of at least 2 and an equivalent weight of at least 200 per isocyanate-reactive group can be used if desired.
The isocyanate-reactive compound(s) may contain dispersed polymer particles. These so-called polymer polyols contain, for example, particles of vinyl polymers such as styrene, acrylonitrile or styrene-acrylonitrile, particles of a polyurea polymer, or polymers of a polyurethane-urea polymer.
In addition, such isocyanate-reactive compounds can be used in admixture with one or more crosslinkers and/or chain extenders. For purposes of this specification, “crosslinkers” are compounds having at least three isocyanate-reactive groups per molecule and an equivalent weight per isocyanate-reactive group of below 200. “Chain extenders” for purposes of this invention have exactly two isocyanate-reactive groups per molecule and have an equivalent weight per isocyanate-reactive group of below 200. In each case, the isocyanate-reactive groups are preferably hydroxyl, primary amino or secondary amino groups. Crosslinkers and chain extenders preferably have equivalent weights of up to 150 and more preferably up to about 125.
Examples of crosslinkers include glycerin, trimethylolpropane, trimethylolethane, diethanolamine, triethanolamine, triisopropanolamine, alkoxylates of any of the foregoing that have equivalent weights of up to 199, and the like. Examples of chain extenders include alkylene glycols (e.g., ethylene glycol, propylene glycol, 1,4-butane diol, 1,6-hexanediol and the like), glycol ethers (such as diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol and the like), ethylene diamine, toluene diamine, diethyltoluene diamine and the like, as well as alkoxylates of any of the foregoing that have equivalent weights of up to 199, and the like.
Examples of suitable polyisocyanates include, for example, m-phenylene diisocyanate, 2,4- and/or 2,6-toluene diisocyanate (TDI), the various isomers of diphenylmethanediisocyanate (MDI), the so-called polymeric MDI products (which are a mixture of polymethylene polyphenylene polyisocyanates in monomeric MDI), carbodiimide-modified MDI products (such as the so-called “liquid MDI” products which have an isocyanate equivalent weight in the range of 135-170), hexamethylene-1,6-diisocyanate, tetramethylene-1,4-diisocyanate, cyclohexane-1,4-diisocyanate, hexahydrotoluene diisocyanate, hydrogenated MDI (H12 MDI), isophorone diisocyanate, naphthylene-1,5-diisocyanate, methoxyphenyl-2,4-diisocyanate, 4,4′-biphenylene diisocyanate, 3,3′-dimethyoxy-4,4′-biphenyl diisocyanate, 3,3′-dimethyldiphenyl methane-4,4′-diisocyanate, 4,4′,4″-triphenylmethane diisocyanate, hydrogenated polymethylene polyphenylpolyisocyanates, toluene-2,4,6-triisocyanate and 4,4′-dimethyldiphenylmethane-2,2′,5,5′-tetraisocyanate. Any of the foregoing that are modified to contain urethane, urea, uretonimine, biuret, allophonate and/or carbodiimide groups may be used.
Preferred isocyanates include TDI. Most preferred isocyanates include MDI and/or polymeric MDI, as well as derivatives of MDI and/or polymeric MDI that contain urethane, urea, uretonimine, biuret, allophanate, and/or carbodiimide groups.
The blowing agent may be a chemical (exothermic) type, a physical (endothermic type) or a mixture of at least one of each type. Chemical types typically react or decompose to produce a carbon dioxide or nitrogen gas under the conditions of the foaming reaction. Water and various carbamate compounds are examples of suitable chemical blowing agents. Physical types include carbon dioxide, various low-boiling hydrocarbons, hydrofluorocarbons, hydroflurochlorocarbons, ethers and the like. Water is most preferred blowing agent, either by itself or in combination with one or more physical blowing agents.
Suitable surfactants are materials that help to stabilize the cells of the foaming reaction mixture until the materials have cured. A wide variety of silicone surfactants as are commonly used in making polyurethane foams can be used in making the foams with the polymer polyols or dispersions of this invention. Examples of such silicone surfactants are commercially available under the tradenames TEGOSTABTM (Evonik Industries/Goldschmidt and Co.), NIAXTM (GE OSi Silicones) and DABCOTM (Air Products and Chemicals).
Suitable catalysts include those described by U.S. Pat. No. 4,390,645, which is incorporated herein by reference. Representative catalysts include:
(a) tertiary amines, such as trimethylamine, triethylamine, N-methylmorpholine, N-ethylmorpholine, N,N-dimethylbenzylamine, N,N-dimethylethanolamine, N,N,N′,N′-tetramethyl-1,4-butanediamine, N,N-dimethylpiperazine, 1,4-diazobicyclo-2,2,2-octane, bis(dimethylaminoethyl)ether, bis(2-dimethylaminoethyl) ether, morpholine,4,4′-(oxydi-2,1-ethanediyl)bis, tri(dimethylaminopropyl)amine, pentamethyldiethylenetriamine and triethylenediamine and the like; as well as so-called “low emissive” tertiary amine catalysts that contain one or more isocyanate-reactive groups such as dimethylaminepropylamine and the like;
(b) tertiary phosphines, such as trialkylphosphines and dialkylbenzylphosphines;
(c) chelates of various metals, such as those which can be obtained from acetylacetone, benzoylacetone, trifluoroacetyl acetone, ethyl acetoacetate and the like with metals such as Be, Mg, Zn, Cd, Pd, Ti, Zr, Sn, As, Bi, Cr, Mo, Mn, Fe, Co and Ni;
(d) acidic metal salts of strong acids, such as ferric chloride, stannic chloride, stannous chloride, antimony trichloride, bismuth nitrate and bismuth chloride;
(e) strong bases, such as alkali and alkaline earth metal hydroxides, alkoxides and phenoxides;
(f) alcoholates and phenolates of various metals, such as Ti(OR)4, Sn(OR)4 and Al(OR)3, wherein R is alkyl or aryl, and the reaction products of the alcoholates with carboxylic acids, beta-diketones and 2-(N,N-dialkylamino)alcohols;
(g) salts of organic acids with a variety of metals, such as alkali metals, alkaline earth metals, Al, Sn, Pb, Mn, Co, Ni and Cu including, for example, sodium acetate, stannous octoate, stannous oleate, lead octoate, metallic driers, such as manganese and cobalt naphthenate; and
(h) organometallic derivatives of tetravalent tin, trivalent and pentavalent As, Sb and Bi and metal carbonyls of iron and cobalt.
The amounts of the various ingredients except for the polyisocyanate are conveniently expressed in parts by weight per 100 parts (“pph”) by weight of the isocyanate-reactive material(s) having at least two isocyanate-reactive groups and equivalent weight of at least 200 per isocyanate-reactive group.
The aminoalcohol compound (i) is present in an effective amount, such as from 0.005 to 5 parts by weight based on the total weight of the reactive mixture, preferably from 0.01 to 0.5 and more preferably from 0.025 to 0.25 parts by weight.
The antioxidant(s) (ii) is present in an effective amount, such as from 0.005 to 5 parts by weight based on the total weight of the reactive mixture, preferably from 0.01 to 0.5 and more preferably from 0.025 to 0.25 parts by weight.
Preferably, the amount of the aminoalcohol (i) and antioxidant (ii) combined is from 0.005 to 5 parts by weight based on the total weight of the reactive mixture, preferably from 0.01 to 0.5 and more preferably from 0.025 to 0.25 parts by weight.
Crosslinkers and/or chain extenders are typically present in small amounts (if at all). A preferred amount is from 0 to 5 pph of crosslinkers and/or chain extenders. A more preferred amount is from 0.05 to 2 pph and a still more preferred amount is from 0.1 to 1 pph of one or more crosslinkers.
Blowing agents are present in amounts sufficient to provide the desired foam density. When water is the blowing agent, a suitable amount is generally from 1.5 to 6 pph, preferably from 2 to 5 pph.
Catalysts are typically present in small amounts, such as up to 2 pph and generally up to 1 pph. A preferred amount of catalyst is from 0.05 to 1 pph.
Surfactants are typically present in amounts up to 5 pph, more typically from 0.1 to 2 pph and preferably from 0.25 to 1.5 pph.
The amount of polyisocyanate that is present is expressed as the “isocyanate index”, which is 100 times the ratio of isocyanate groups to isocyanate-reactive groups in the foam formulation. The isocyanate index is typically from about 70 to 150. A preferred isocyanate index is from 80 to 125 and a more preferred isocyanate index is from 80 to 115. In some embodiments, the isocyanate index is from 90 to 115 or from 95 to 115.
Other ingredients may be present during the foaming step, including, for example, fillers, colorants, odor masks, flame retardants, biocides, antistatic agents, thixotropic agents and cell openers.
Polyurethane foam is made in accordance with this invention by forming a reaction mixture containing the various ingredients and curing the reaction mixture. Free-rise process such as continuous slabstock production methods can be used. Alternatively, molding methods can be used. Such processes are well known. Generally, no alternation of conventional processing operations is needed to produce polyurethane foam in accordance with this invention (other than the inclusion of the beta-diketo amine compound together with the antioxidant(s)).
The various ingredients may be introduced individually or in various subcombinations into a mix head or other mixing device where they are mixed and dispensed into a region (such as a trough or other open container, or a closed mold) where they are cured. It is often convenient to supply the aminoalcohol compound in the form of a solution in water or other suitable solvent. Alternatively (or in addition), the aminoalcohol compound may be mixed with the isocyanate-reactive compound(s) beforehand. It is often convenient, especially when making molded foam, to form a formulated polyol component that contains the isocyanate-reactive compound(s), including crosslinkers and/or chain extenders as may be used, the aminoalcohol compound(s), the antioxidant(s) and optionally the catalyst(s), surfactant(s) and blowing agent(s). This formulated polyol component is then contacted with the polyisocyanate (as well as any other ingredients that are not present in the formulated polyol component) to produce the foam.
It is preferred to blend the aminoalcohol compound with the isocyanate reactive compound(s) that have at least two isocyanate-reactive groups per molecule and an equivalent weight of at least 200 per isocyanate-reactive group, prior to forming the polyurethane foam and to maintain that blend at approximately room temperature or a higher temperature (but below the boiling temperature of the aminoalcohol compound and below the temperature at which the polyol degrades) for a period of at least 30 minutes prior to making the foam.
Some or all of the various components may be heated prior to mixing them to form the reaction mixture. In other cases, the components are mixed at ambient temperatures (such as from 15-40° C.). Heat may be applied to the reaction mixture after all ingredients have been mixed, but this is often unnecessary.
The product of the curing reaction is a flexible polyurethane foam. The foam density may be from 20 to 200 kg/m3. For most seating and bedding applications, a preferred density is from 24 to 80 kg/m3. The foam may have a resiliency of at least 50% on the ball rebound test of ASTM 3574-H. Foams produced in accordance with this invention are useful, for example, in cushioning applications such as bedding and domestic, office or vehicular seating, as well as in other vehicular applications such as headrests, dashboards instrument panels, armrests or headliners.
Polyurethane foams made in accordance with the invention are characterized in having low formaldehyde and low acetaldehyde emissions. A suitable method for measuring formaldehyde and acetaldehyde emissions is as follows: The polyurethane foam sample is crushed to open the cells. The crushed foam is cut into 100 mm x 80 mm x 50 mm samples, which are immediately covered with aluminum foil and kept in this manner for 3 to 14 days at about 25° C. A polyvinyl fluoride (PVF) gas bag is used for aldehyde emission test. Before testing, the gas bags are heated in oven at 95° C. overnight, and washed with pure nitrogen three times before put foam samples in gas bag. A blank gas bag is employed as blank sample during the analysis. After the foam samples are put into gas bag, the gas bag is filled with nitrogen gas, and then heated in the oven for 2 hours at 65° C. After heating, the nitrogen gas from the gas bags are captured in a dinitrophenylhydrazine (DNPH) cartridge. The DNPH cartridge is then washed with solvent and the eluent is analyzed for aldehydes such as formaldehyde and acetaldehyde by liquid chromatography. Preferably, the formaldehyde and acetaldehyde emissions each are no greater than 70% of comparable sample, more preferably no greater than 50% of comparable sample, as measured according to this method. In one embodiment, the polyurethane foam made by the process of the present invention exhibits formaldehyde and acetaldehyde emissions each no greater than 1 μg for a 100mm by 80 mm by 50 mm test piece.
The following examples are provided to illustrate the invention, but are not intended to limit the scope thereof. All parts and percentages are by weight unless otherwise indicated.
For Examples 1 to 4 formulated A-side (comprising isocyanate and other additives) and B-side (polyol blend comprising polyols and other additives) are made from the components listed herein below, amounts are given in grams (g).
Polyol formulations are neat (i.e., without an aminoalcohol (AA) and/or an antioxidant (AO)) or prepared by mixing with an aminoalcohol or an aminoalcohol and an antioxidant for 3 minutes at 3000 rpm to make sure the aminoalcohol and antioxidant is well mixed with polyol. The polyols are stored at room temperature for 0 to 2 weeks before foaming experiment. After foaming, the foam samples are immediately covered with aluminum foil and kept at room temperature before being analyzed by a gas bag method.
In Table 1:
“Polyol-1” is a glycerine initiated propylene oxide and 15 percent ethylene oxide capped polyol having a hydroxyl number of 27.5 and an equivalent weight of 2040 available as VORANOL™ CP 6001 Polyol from The Dow Chemical Company;
“Polyol-2” is a grafted polyether polyol containing 40 wt% copolymerized styrene and acrylonitrile solids and an OH number of 22 mg KOH/g available as SPECFLEX™ NC-701 from The Dow Chemical Company;
“DEOA” is diethanolamine, a crosslinker, available from SCR Co., Ltd.;
“Glycerine” is a crosslinker available from SCR Co., Ltd.;
“TEDA” is a 33 percent triethylene diamine in dipropylene glycol curing catalyst is available as DABCO 33 LV from Air Products;
“TA/G” is a tertiary amine/glycol mixture available as C225 from Momentive Co., Ltd.;
“B 8727” is an organosilicone surfactant available TEGOSTAB B8727 LF2 by Evonik Industries/Goldschmidt Chemical Corporation;
“AO-1” is a butylated hydroxytoluene (BHT) and amine-free liquid heat stabilizer blend available as IRGASTAB™ PUR 68 from BASF (China) Co., Ltd;
“AO-2” is hindered phenolic primary antioxidant comprising a benzenepropanoic acid, 3,5-bis (1,1-dimethyl-ethyl)-4-hydroxy-C7-C9 branched alkyl esters available as IRGANOXTM 1135 from BASF (China) Co., Ltd;
“AO-3” is sterically hindered primary phenolic antioxidant stabilizer available as IRGANOX 1076 from BASF (China) Co., Ltd:
“AO-4” is a 1:1:1 mixture of AO-1, AO-2, and AO-3;
“AA-1” is 2-amino-2(hydroxymethyl)propane-1,3-diol available from SCR Co., Ltd.;
“MDI” is a 3.2 functional polymeric MDI with 30.4% NCO and an isocyanate equivalent weight of 138 available as PAPITM 27 Isocyanate from The Dow Chemical Company;
“TDI” is toluene diisocyanate having a functionality of 2 with an isocyanate equivalent weight of 87, available as VORANATE T-80 Type I TDI from The Dow Chemical Company; and
“TM-20” is a mixture of 20% of MDI and 80% TDI by weight.
The compositions of Examples 1 to 4 are shown in Table 1.
Examples 1 to 4 are foamed by mixing an aliquot of 100 g of the polyol (B-side) with 28 g of TM-20 (A-side) to prepare the foam sample. After foaming, the foam sample is packaged with aluminum foil before analysis. The gas bag analysis is conducted within 7 days after the foam sample is prepared.
1dissolved in 6 g water and added to polyol
Aldehydes emitted from the foam samples are analyzed by the following gas bag method: Sample Preparation. The foam samples (30 g, cut into cubicles) are put into a 10 L Tedlar gas bag (Delin Co. ltd, China) for analysis. The gas bag is washed with pure nitrogen three times before analysis, and a blank gas bag is employed as blank during the analysis. After the foam sample is put into the gas bag, the gas bag is filled with about 7 L of nitrogen gas, and then heated in the oven for 2 hours at 65° C. The nitrogen gas in the gas bag is then pumped out by an air pump for VOCs and carbonyls analysis.
Analytical Method. For the aldehyde test, a DNPH cartridge (CNWBOND DNPH-Silica cartridge, 350 mg, Cat. No. SEEQ-144102, Anple Co., Ltd.) is employed to absorb the carbonyls emitted from the gas bag. The sampling speed is 330 mL/min and the sampling time is 13 min. After absorption, the DNPH cartridge is eluted with 3 g (precisely weight) of ACN, and the ACN solution is analyzed by HPLC to quantify the carbonyls in the sample. The standard solution with six DNPH derivatives (TO11A carbonyl-DNPH mix, Cat. No. 48149-U, 15 ppm for each individual compound, Supelco Co., Ltd) is diluted by acetonitrile and the final solution (0.794 ppm wt/wt) is restored in a 2 ml vial for instrument calibration at −4° C. (refrigerator). The 0.794 ppm (wt/wt) standard solution prepared is injected into the HPLC system as a one point external standard for quantification of carbonyls in the sample. The first two peaks are identified as formaldehyde and acetaldehyde according to the standard specification.
The response factor is calculated for each derivative according the formula below:
where:
The concentration of the aldehyde-DNPH derivative in the sample solution is calculated based on the formula below:
where:
The HPLC conditions are shown in Table 2:
The gas bag analysis results for aldehydes reduction for Examples 1 to 4 are shown in Table 3.
As can be seen by the data presented in Table 3, the examples of the present invention are effective as aldehyde scavenger in polyol/foam product. Further, it is shown that the aminoalcohol compound shows a synergic effect with antioxidants to abate aldehydes in polyol/foam product.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2017/073764 | 2/16/2017 | WO | 00 |
