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US4523025A Expired / Lapsed US ⏱️ 0.0 years remaining

Polymer polyols from partially reacted polyamines

Assignee: Dow Chemical Co
•
Filing: 1983-10-21
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Granted: 1985-06-11
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Expires: 2003-10-21
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Abstract

Abstract A polymer polyol made by the reaction of a partially reacted polyamine with an organic polyisocyanate in a polyether polyol solvent of about 3,000 to 8,000 molecular weight is disclosed. Preferably, the polyisocyanate is reacted with a partially alkoxylated polyoxyalkylenediamine. This polymer polyol may be used in the manufacture of flexible polyurethane foams with improved properties. The polymer polyols are more stable than those made by other procedures.

Inventors

  • 👤 Michael Cuscurida
  • 👤 Howard P. Klein

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 13:48
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/48; C08G18/50; C08G18/5021; C08G18/08; C08G18/0838; C08G18/0842; C08G18/0847; C08G18/0852; C08G18/0857; C08G18/5036; Y; Y10; Y10T; Y10T428/00; Y10T428/24; Y10T428/24479; Y10T428/24496; Y10T428/24504; Y10T428/24512

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 208 words
A polymer polyol made by the process comprising a. reacting (1) a compound selected from the group consisting of compounds of the formulae ##STR3## where R is an alkyl group of from 1 to 4 carbon atoms, n ranges from 1 to 35, y ranges from 1 to 5 and where I is a trifunctional initiator selected from the group consisting of glycerine, trimethylolpropane and triethanolamine with (2) a compound selected from the group consisting of alkylene oxides having 2 to 8 carbon atoms to give an adduct where the tertiary amine content of the resulting adduct is less than 90%, and b. subsequently reacting (1) the adduct from step a. with (2) An organic polyisocyanate selected from the group consisting of toluene diisocyanate, diphenylmethane diisocyanate, isophorone diisocyanate and methylene biscyclohexylisocyanate in the presence of (3) a polyether polyol solvent having a molecular weight of about 3,000 to 8,000 a hydroxyl number between about 20 and 60 and a hydroxyl functionality of from about 2 to about 4 such that the ratio of equivalents of the adduct to equivalents of polyisocyanate is from about 1:1 to 2:1 and the combined weight of the adduct and the polyisocyanate is about 5 to 25 wt% of the polyether polyol solvent.
Claim 2
Dependent Claim 208 words
A polymer polyol made by the process comprising a. reacting (1) a compound selected from the group consisting of compounds of the formulae ##STR3## where R is an alkyl group of from 1 to 4 carbon atoms, n ranges from 1 to 35, y ranges from 1 to 5 and where I is a trifunctional initiator selected from the group consisting of glycerine, trimethylolpropane and triethanolamine with (2) a compound selected from the group consisting of alkylene oxides having 2 to 8 carbon atoms to give an adduct where the tertiary amine content of the resulting adduct is less than 90%, and b. subsequently reacting (1) the adduct from step a. with (2) An organic polyisocyanate selected from the group consisting of toluene diisocyanate, diphenylmethane diisocyanate, isophorone diisocyanate and methylene biscyclohexylisocyanate in the presence of (3) a polyether polyol solvent having a molecular weight of about 3,000 to 8,000 a hydroxyl number between about 20 and 60 and a hydroxyl functionality of from about 2 to about 4 such that the ratio of equivalents of the adduct to equivalents of polyisocyanate is from about 1:1 to 2:1 and the combined weight of the adduct and the polyisocyanate is about 5 to 25 wt% of the polyether polyol solvent.
Claim 3
Dependent Claim 59 words
The polymer polyol of claim 15 in which the reactants in step a. are a. a compound of the formula ##STR4## where R is an alkyl group of from 1 to 4 carbon atoms and n ranges from 1 to 35 and b. an alkylene oxide selected from the group consisting of ethylene oxide, 1,2-propylene oxide and mixtures thereof.
Claim 4
Dependent Claim 25 words
The polymer polyol of claim 1 where step a. is conducted in the presence of 1 to 15 wt.% water based on the polyamine quantity.
Claim 5
Dependent Claim 23 words
The polymer polyol of claim 1 where step a. is conducted at a temperature in the range of 75° C. to 135° C.
Claim 6
Dependent Claim 205 words
A polymer polyol made by the process comprising a. reacting (1) a compound of the formula ##STR5## where R is an alkyl group of from 1 to 4 carbon atoms and n ranges from 1 to 35 with (2) an alkylene oxide selected from the group consisting of ethylene oxide, 1,2-propylene oxide and mixtures thereof in the presence of 1 to 15 wt.% water based on the polyamine quantity, at a temperature in the range of 75° C. to 135° C. to give an adduct where the tertiary amine content of the resulting adduct is less than 90% and b. subsequently reacting (1) the adduct from step a. with (2) an organic polyisocyanate selected from the group consisting of toluene diisocyanate, diphenylmethane diisocyanate, isophorone diisocyanate and methylene bis-cyclohexylisocyanate in the presence of (3) a polyether polyol solvent having a molecular weight of about 3,000 to 8,000, a hydroxyl number between about 20 and 60 and a hydroxyl functionality of from about 2 to about 4 such that the ratio of equivalents of the adduct to equivalents of polyisocyanate is from about 1:1 to 2:1 and the combined weight of the adduct and the polyisocyanate is about 5 to 25 wt% of the polyether polyol solvent.
Claim 7
Dependent Claim 205 words
A polymer polyol made by the process comprising a. reacting (1) a compound of the formula ##STR5## where R is an alkyl group of from 1 to 4 carbon atoms and n ranges from 1 to 35 with (2) an alkylene oxide selected from the group consisting of ethylene oxide, 1,2-propylene oxide and mixtures thereof in the presence of 1 to 15 wt.% water based on the polyamine quantity, at a temperature in the range of 75° C. to 135° C. to give an adduct where the tertiary amine content of the resulting adduct is less than 90% and b. subsequently reacting (1) the adduct from step a. with (2) an organic polyisocyanate selected from the group consisting of toluene diisocyanate, diphenylmethane diisocyanate, isophorone diisocyanate and methylene bis-cyclohexylisocyanate in the presence of (3) a polyether polyol solvent having a molecular weight of about 3,000 to 8,000, a hydroxyl number between about 20 and 60 and a hydroxyl functionality of from about 2 to about 4 such that the ratio of equivalents of the adduct to equivalents of polyisocyanate is from about 1:1 to 2:1 and the combined weight of the adduct and the polyisocyanate is about 5 to 25 wt% of the polyether polyol solvent.

References Cited (Backward Citations)

US4296213A Cited
US4309532A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-06-10 1988-12-10 1989-06-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-06-10 1992-12-10 1993-06-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-06-10 1996-12-10 1997-06-11 $7700.00 Window Closed / Lapsed

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