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US4444920A Expired / Lapsed US ⏱️ 0.0 years remaining

Aromatic polyols made from alkylene glycols and waste streams from the manufacture of dimethyl terephthalate containing methyl p-formylbenzoate

Assignee: Dow Chemical Co
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Filing: 1983-03-18
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Granted: 1984-04-24
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Expires: 2003-03-18
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Abstract

Abstract Mixtures of aromatic polyols containing ester functionalities suitable for use in rigid foams prepared by reacting a dimethyl terephthalate waste stream containing methyl p-formylbenzoate over a metal alkoxide catalyst and subsequently transesterifying the product with a polyalkylene glycol in the presence of heat are described. These novel polyols may be blended with conventional polyols to yield excellent rigid foams, thus serving as useful polyol extenders. These low hydroxyl number extender polyols unexpectedly have a low relative viscosity.

Inventors

  • 👤 Michael E. Brennan

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 15:25
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/42; C08G18/4244; C08G18/4247; C08G18/4205; C08G18/4208; C08G18/4225; C08G2115/00; C08G2115/02

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 71 words
A mixture of aromatic polyols having hydroxyl and ester functionalities for use in preparing rigid foams, being produced by the process comprising (a) reacting a dimethyl terephthalate waste stream which contains from about 40 to 60 mole percent of methyl p-formylbenzoate over a metal alkoxide catalyst and (b) subsequently transesterifying the product from step (a) with a polyalkylene glycol by applying heat in the range from about 150° to 250° C.
Claim 2
Dependent Claim 71 words
A mixture of aromatic polyols having hydroxyl and ester functionalities for use in preparing rigid foams, being produced by the process comprising (a) reacting a dimethyl terephthalate waste stream which contains from about 40 to 60 mole percent of methyl p-formylbenzoate over a metal alkoxide catalyst and (b) subsequently transesterifying the product from step (a) with a polyalkylene glycol by applying heat in the range from about 150° to 250° C.
Claim 3
Dependent Claim 36 words
The mixture of aromatic polyols of claim 1 in which the dimethyl terephthalate production waste stream also contains one or more of the compounds from the group consisting of dimethyl terephthalate, p-methyltoluate, methylbenzoate and p-toluic acid.
Claim 4
Dependent Claim 28 words
The mixture of aromatic polyols of claim 1 in which the metal in the metal alkoxide catalyst is selected from Groups IA and IIIA of the Periodic Table.
Claim 5
Dependent Claim 46 words
The mixture of aromatic polyols of claim 1 in which the metal alkoxide catalyst is dissolved or suspended in methanol and is selected from the group consisting of sodium alkoxide and aluminum alkoxide where the alkyl group present therein has from one to four carbon atoms.
Claim 6
Dependent Claim 23 words
The mixture of aromatic polyols of claim 1 in which the catalyst concentration in step (a) ranges from 1 to 10 weight percent.
Claim 7
Dependent Claim 37 words
The mixture of aromatic polyols of claim 1 in which the alkylene glycol has the formula ##STR3## where R is hydrogen or lower alkyl of 1 to 4 carbon atoms and n is from 1 to 10.
Claim 8
Dependent Claim 17 words
The mixture of polyols of claim 1 in which the alkylene glycol is a glycol waste stream.
Claim 9
Dependent Claim 31 words
The mixture of polyols of claim 1 in which the reactions are conducted at a temperature between about 25° to 250° C. and at a pressure between one atmosphere and subatmospheric.
Claim 10
Dependent Claim 23 words
The mixture of polyols of claim 1 in which the average hydroxyl number of the resultant mixture is between about 100 and 500.
Claim 11
Dependent Claim 26 words
The mixture of aromatic polyols of claim 1 in which the amount of alkylene glycol employed is 1-5 equivalents based on the dimethyl terephthalate waste stream.
Claim 12
Dependent Claim 133 words
A mixture of aromatic polyols having hydroxyl and ester functionalities for use in preparing rigid foams, being produced by the process comprising (a) reacting a waste stream from the manufacture of dimethyl terephthalate which contains dimethyl terephthalate and from about 40 to 60 mole percent of methyl p-formylbenzoate over a catalyst selected from the group consisting of sodium alkoxide and aluminum alkoxide where the alkyl group is from one to four carbon atoms and (b) subsequently transesterifying the product from step (a) with an alkylene glycol residue containing one or more alkylene glycols having the formula ##STR4## where R is hydrogen or lower alkyl of 1 to 4 carbon atoms and n is from 1 to 10, by heating the mixture at a temperature in the range from about 150° to 250° C.
Claim 13
Dependent Claim 133 words
A mixture of aromatic polyols having hydroxyl and ester functionalities for use in preparing rigid foams, being produced by the process comprising (a) reacting a waste stream from the manufacture of dimethyl terephthalate which contains dimethyl terephthalate and from about 40 to 60 mole percent of methyl p-formylbenzoate over a catalyst selected from the group consisting of sodium alkoxide and aluminum alkoxide where the alkyl group is from one to four carbon atoms and (b) subsequently transesterifying the product from step (a) with an alkylene glycol residue containing one or more alkylene glycols having the formula ##STR4## where R is hydrogen or lower alkyl of 1 to 4 carbon atoms and n is from 1 to 10, by heating the mixture at a temperature in the range from about 150° to 250° C.
Claim 14
Dependent Claim 23 words
The mixture of aromatic polyols of claim 11 in which the catalyst concentration in step (a) ranges from 1 to 10 weight percent.
Claim 15
Dependent Claim 31 words
The mixture of polyols of claim 11 in which the reactions are conducted at a temperature between about 25° to 250° C. and at a pressure between one atmosphere and subatmospheric.
Claim 16
Dependent Claim 23 words
The mixture of polyols of claim 11 in which the average hydroxyl number of the resultant mixture is between about 100 and 500.
Claim 17
Dependent Claim 26 words
The mixture of aromatic polyols of claim 11 in which the amount of alkylene glycol employed is 1-5 equivalents based on the dimethyl terephthalate waste stream.
Claim 18
Independent Claim 70 words
A method for making a mixture of aromatic polyols having hydroxyl and ester functionalities for use in preparing rigid foams comprising (a) reacting a dimethyl terephthalate waste stream which contains from 40 to 60 mole percent of methyl p-formylbenzoate over a metal alkoxide catalyst and (b) subsequently transesterifying the product from step (a) with a polyalkylene glycol by heating the mixture to a temperature between about 150° and 250° C.
Claim 19
Independent Claim 70 words
A method for making a mixture of aromatic polyols having hydroxyl and ester functionalities for use in preparing rigid foams comprising (a) reacting a dimethyl terephthalate waste stream which contains from 40 to 60 mole percent of methyl p-formylbenzoate over a metal alkoxide catalyst and (b) subsequently transesterifying the product from step (a) with a polyalkylene glycol by heating the mixture to a temperature between about 150° and 250° C.
Claim 20
Dependent Claim 77 words
The method of claim 16 in which (a) the metal alkoxide catalyst is selected from the group consisting of sodium alkoxide and aluminum alkoxide where the alkyl group has from one to four carbon atoms, and (b) the alkylene glycol is an alkylene glycol residue having at least one alkylene glycol with the formula ##STR5## where R is hydrogen or lower alkyl of 1 to 4 carbon atoms and n is from 1 to 10 carbon atoms.
Claim 21
Dependent Claim 163 words
A rigid polyurethane foam obtained by reacting in the presence of a blowing agent and a catalyst of polyurethane formation, an organic polyisocyanate and a polyol blend comprising (a) from about 5 to 100 percent by weight of a mixture of aromatic polyols having ester functionalities which is the reaction product from (1) reacting a dimethyl terephthalate waste stream which contains from about 40 to 60 mole percent of methyl p-formylbenzoate over a metal alkoxide catalyst and (2) subsequently transesterifying the product from step (1) with a polyalkylene glycol by applying heat in the range from about 150° to 250° C., and (b) from about 95 to 0 percent by weight of a nitrogen-containing polyol which is the reaction product from (1) reacting one mole of phenol or nonylphenol with one to two moles of diethanolamine and formaldehyde to give a Mannich reaction product, and (2) subsequently reacting one mole of the Mannich reaction product with 2 to 3 moles of propylene oxide.
Claim 22
Dependent Claim 163 words
A rigid polyurethane foam obtained by reacting in the presence of a blowing agent and a catalyst of polyurethane formation, an organic polyisocyanate and a polyol blend comprising (a) from about 5 to 100 percent by weight of a mixture of aromatic polyols having ester functionalities which is the reaction product from (1) reacting a dimethyl terephthalate waste stream which contains from about 40 to 60 mole percent of methyl p-formylbenzoate over a metal alkoxide catalyst and (2) subsequently transesterifying the product from step (1) with a polyalkylene glycol by applying heat in the range from about 150° to 250° C., and (b) from about 95 to 0 percent by weight of a nitrogen-containing polyol which is the reaction product from (1) reacting one mole of phenol or nonylphenol with one to two moles of diethanolamine and formaldehyde to give a Mannich reaction product, and (2) subsequently reacting one mole of the Mannich reaction product with 2 to 3 moles of propylene oxide.
Claim 23
Dependent Claim 24 words
The rigid polyurethane foam of claim 18 in which the polyol blend has an average hydroxyl number in the range from 100 to 500.

References Cited (Backward Citations)

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-04-24 1987-10-24 1988-04-24 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-04-24 1991-10-24 1992-04-24 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-04-24 1995-10-24 1996-04-24 $7700.00 Window Closed / Lapsed

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