AROMATIC POLYESTER POLYOL COMPOUND
A method for making an aromatic polyester polyol compound, wherein the method comprises reacting at esterification reaction conditions a reactive mixture comprising the following components: (i) an aromatic acid compound; (ii) an aliphatic diol compound; (iii) a dialkylol alkanoic acid compound; (iv) optionally, a hydrophobic compound, a polyhydroxy compound comprising at least three hydroxyl groups, or combinations thereof, and wherein the aromatic polyester polyol compound is liquid at 25° C. and has a hydroxy value ranging from about 30 to about 600.
1 . A method for making an aromatic polyester polyol compound, wherein the method comprises reacting at esterification reaction conditions a reactive mixture comprising the following components:
(i) an aromatic acid compound;
(ii) an aliphatic diol compound;
(iii) a dialkylol alkanoic acid compound of Formula I:
wherein R is hydrogen, C 1 to C 8 alkyl (straight-chain or branched), C 1 to C 8 hydroxyalkyl, C 1 to C 12 aromatic, or C 1 to C 12 cyclic aliphatic, and wherein R 1 , R 2 are each independently hydrogen, C 1 to C alkyl (straight-chain or branched); and
(iv) optionally, a hydrophobic compound, a polyhydroxy compound comprising at least three hydroxyl groups, or combinations thereof; and
wherein the aromatic polyester polyol compound is liquid at 25° C. and has a hydroxy value ranging from about 30 to about 600.
2 . The method according to claim 1 , wherein at least one of R 1 and R 2 is hydrogen.
3 . The method according to claim 1 , wherein R is hydrogen, ethyl, methyl, hydroxymethyl, C 1 to C 3 alkyl, or phenyl.
4 . The method according to claim 1 , wherein Component (iii) comprises 2,2-bis(hydroxymethyl)propionic acid (DMPA); 2,2-bis(hydroxymethyl)butanoic acid (DMBA); 2,2-bis(hydroxymethyl)pentanoic acid (DMPTA); 2,2-bis(hydroxymethyl)hexanoic acid (DMHA); 2,2,2-trimethylol acetic acid (TMAA); and 2,2-bis(hydroxymethyl)phenylacetic acid and 2,2-bis(hydroxymethyl) tolylacetic acid; or combinations thereof.
5 . The method according to claim 1 , wherein the aromatic polyester polyol compound has a bio-renewable and/or recycled content of at least 10% by weight based on the total weight of the aromatic polyester polyol.
6 . (canceled)
7 . The method according to claim 1 , wherein the viscosity of the aromatic polyester polyol compound ranges from about 200 to about 150,000 centipoises at 25° C.
8 . The method according to claim 1 , wherein the acid value of the aromatic polyester polyol compound ranges from about 0.1 mg of KOH/g to about 10 mg of KOH/g.
9 . The method according to claim 1 , wherein the viscosity of the aromatic polyester polyol compound is lower than a corresponding polyol compound made to the same hydroxy number, aromatic content, and calculated functionality but without the use of Component (iii).
10 . The method according to claim 1 , wherein the aromatic polyester polyol compound comprises an average functionality ranging from about 1.5 to about 3.5, an average hydroxyl number ranging from about 30 to about 600, and an acid number ranging from about 0.1 to about 10, and has a resulting viscosity ranging from 200 to about 50,000 centipoises at about 25° C.
11 . The method according to claim 1 , wherein the esterification reaction conditions comprise reacting the reactive mixture at a temperature ranging from about 50° C. to about 300° C. for a period ranging from about 1 hour to about 24 hours.
12 . The method according to claim 1 , wherein the reactive mixture further comprises (vi) an esterification catalyst compound and wherein the esterification catalyst compound comprises about 0.001 to about 0.2% by weight based on the weight of the reactive mixture.
13 . An aromatic polyester compound, wherein the aromatic polyester polyol compound is the reaction product of a reactive mixture comprising the following components:
(i) an aromatic acid compound;
(ii) an aliphatic diol compound;
(iii) a dialkylol alkanoic acid compound of Formula I:
wherein R is hydrogen, C 1 to C 8 alkyl (straight-chain or branched), C 1 to C 8 hydroxyalkyl, C 1 to C 12 aromatic, or C 1 to C 12 cyclic aliphatic, and wherein R 1 , R 2 are each independently hydrogen, C 1 to C 8 alkyl (straight-chain or branched); and
(v) optionally, a hydrophobic compound, a polyhydroxy compound comprising at least three hydroxyl groups, or combinations thereof; and
wherein the aromatic polyester polyol compound is liquid at 25° C. and has a hydroxy value ranging from about 30 to about 600.
14 . The aromatic polyester polyol compound according to claim 13 , wherein at least one of R 1 and R 2 is hydrogen.
15 . The aromatic polyester polyol compound according to claim 13 , wherein R is hydrogen, ethyl, methyl, hydroxymethyl, C 1 -C 3 alkyl, or phenyl.
16 . The aromatic polyester polyol compound according to claim 13 , wherein Component (iii) comprises 2,2-bis(hydroxymethyl)propionic acid (DMPA); 2,2-bis(hydroxymethyl)butanoic acid (DMBA); 2,2-bis(hydroxymethyl)pentanoic acid (DMPTA); 2,2-bis(hydroxymethyl)hexanoic acid (DMHA); 2,2,2-trimethylol acetic acid (TMAA); and 2,2-bis(hydroxymethyl)phenylacetic acid and 2,2-bis(hydroxymethyl) tolylacetic acid; or combinations thereof.
17 . The aromatic polyester polyol compound according to claim 13 , wherein the aromatic polyester polyol has a bio-renewable content and/or recycled content of at least 10% by weight based on the total weight of the aromatic polyester polyol.
18 . (canceled)
19 . The aromatic polyester polyol compound according to claim 13 , wherein the viscosity of the aromatic polyester polyol compound ranges from about 200 to about 150,000 centipoises at 25° C.
20 . The aromatic polyester polyol compound according to claim 13 , wherein the acid value of the aromatic polyester polyol compound ranges from about 0.1 mg of KOH/g to about 10 mg of KOH/g.
21 . The aromatic polyester polyol compound according to claim 13 , wherein the viscosity of the aromatic polyester polyol compound is lower than a corresponding polyol compound made to the same hydroxy number, aromatic content, and calculated functionality but without the use of Component (iii).
22 . The aromatic polyester polyol compound according to claim 13 , wherein the aromatic polyester polyol comprises an average functionality ranging from about 1.5 to about 3.5, an average hydroxyl number ranging from about 30 to about 600, and an acid number ranging from about 0.1 to about 10, and has a resulting viscosity ranging from 200 to about 50,000 centipoises at about 25° C.
23 . A polyurethane foam composition comprising:
(a) an isocyanate compound;
(b) an aromatic polyester polyol compound that is the esterification reaction product of the following components:
(i) an aromatic acid compound;
(ii) an aliphatic diol compound;
(iii) a dialkylol alkanoic acid compound of Formula I:
wherein R is hydrogen, C 1 to C 8 alkyl (straight-chain or branched), C 1 to C 8 hydroxyalkyl, C 1 to C 12 aromatic, or C 1 to C 12 cyclic aliphatic, and wherein R 1 , R 2 are each independently hydrogen, C 1 to C 8 alkyl (straight-chain or branched); and
(iv) optionally, a hydrophobic compound, a polyhydroxy compound comprising at least three hydroxyl groups, or combinations thereof; and
wherein the aromatic polyester polyol compound is liquid at 25° C. and has a hydroxy value ranging from about 30 to about 600; and
(c) optionally, a blowing agent; and
(d) optionally, auxiliary compounds and additives.