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US4309527A Expired / Lapsed US ⏱️ 0.0 years remaining

Fire retardant polymer resin

Assignee: Fiber Materials Inc
•
Filing: 1981-02-09
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Granted: 1982-01-05
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Expires: 2001-02-09
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Abstract

Abstract Flame retardant polymer resins formed by an acid condensation reaction from a mixture of resorcinol and furfural with a molar excess of the aldehyde. In one particular embodiment the resin is formed of a mixture of two prepolymer solutions with at least a boric acid catalyst, one or both of the prepolymer solutions being an acid-condensation reaction product of resorcinol and furfural with excess aldehyde functionality, or one of the prepolymers being a mix of substantially unreacted resorcinol and furfural with a slight molar excess of aldehyde.

Inventors

  • 👤 Lawrence E. McAllister
  • 👤 Herbert Dietrich

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 21:31
CPC Classifications
C; C08; C08J; C08J9/00; C08J9/04; C08J9/12; C08J9/14; C08J9/143; C08G; C08G8/00; C08G8/04; C08G8/06; C08G8/08; C08G8/20; C08G8/22; C08G8/24; C08J2361/00; C08J2361/04; C08J2361/06

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 216 words
A flame retardant polymer resin prepared according to the method comprising the steps of reacting moities of a first aldehyde and first phenol in the presence of a mineral acid in sufficient proportions to provide an acid-condensation reaction product in the form of a relatively low molecular weight, low viscosity, liquid linear polymer having excess aldehyde functionality, said first aldehye being selected from the group consisting of furfural and mixtures of furfural and paraformaldehyde, said first phenol being selected from the group consisting of metacresol, orthocresol, 3,5 dimethylphenol, resorcinol and substituted resorcinols; mixing moities of a second aldehyde and second phenol to provide a solution of said second phenol in said second aldehyde, which solution is separate from said reaction product and contains said aldehyde in molar excess, said second aldehyde and second phenol being selected from the same groups as said first aldehyde and first phenol; adding to said reaction product a solid, organic, watersoluble acid as a polymerization active catalyst; adding to said solution an inorganic acid polymerization catalyst containing water of hydration, said inorganic acid being selected from the group consisting of boric acid and boric acid complexes; and reacting a mixture of said reaction product and said solution in the presence of said catalysts to produce condensation polymerization thereof into said resin.
Claim 2
Dependent Claim 216 words
A flame retardant polymer resin prepared according to the method comprising the steps of reacting moities of a first aldehyde and first phenol in the presence of a mineral acid in sufficient proportions to provide an acid-condensation reaction product in the form of a relatively low molecular weight, low viscosity, liquid linear polymer having excess aldehyde functionality, said first aldehye being selected from the group consisting of furfural and mixtures of furfural and paraformaldehyde, said first phenol being selected from the group consisting of metacresol, orthocresol, 3,5 dimethylphenol, resorcinol and substituted resorcinols; mixing moities of a second aldehyde and second phenol to provide a solution of said second phenol in said second aldehyde, which solution is separate from said reaction product and contains said aldehyde in molar excess, said second aldehyde and second phenol being selected from the same groups as said first aldehyde and first phenol; adding to said reaction product a solid, organic, watersoluble acid as a polymerization active catalyst; adding to said solution an inorganic acid polymerization catalyst containing water of hydration, said inorganic acid being selected from the group consisting of boric acid and boric acid complexes; and reacting a mixture of said reaction product and said solution in the presence of said catalysts to produce condensation polymerization thereof into said resin.

References Cited (Backward Citations)

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US2504100A Cited
US2744875A Cited
US2859205A Cited
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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) 1985-01-04 1985-07-06 1986-01-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-01-04 1989-07-06 1990-01-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-01-04 1993-07-06 1994-01-05 $7700.00 Window Closed / Lapsed

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