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US3927140A Expired / Lapsed US ⏱️ 0.0 years remaining

Adhesive composition

Assignee: Research Corp
•
Filing: 1973-10-24
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Granted: 1975-12-16
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Expires: 1993-10-24
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Abstract

Abstract An aldehyde condensation copolymer is disclosed which is formed by co-condensing A. 90% - 10% BY WEIGHT OF AN ESSENTIALLY LINEAR AND NONCROSSLINKABLE ALDEHYDE CONDENSATION PREPOLYMER WITH B. 10% - 90% BY WEIGHT OF A HIGHLY THERMOSETTABLE AND CROSSLINKABLE ALDEHYDE CONDENSATION PREPOLYMER.

Inventors

  • 👤 James T Rice
  • 👤 Chia M Chen

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 19:02
CPC Classifications
C; C08; C08G; C08G12/00; C08G12/02; C08G8/00; C08G8/04; C09; C09J; C09J161/00

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 257 words
A METHOD FOR FORMING AN ALDEHYDE-PHENOLIC CONDENSATION COPOLYMER, WHICH COMPRISES: FORMING AN ESSENTIALLY LINEAR AND NON-CROSS-LINKABLE ALDEHYDE CONDENSATION PREPOLYMER HAVING A VISCOSITY OF 5 CPS TO 75 CPS AT 25*C BY REACTING AN ALDEHYDE SELECTED FROM THE GROUP CONSISTING OF FORMALDEHYDE ACETALDEHYDE, BENZALKEHYDE, PROPIONALDEHYDE, BUTYRALDEHYDE, FURFURALDEHYDE, AND MIXTURES THEREOF WITH A PHENOLIC COMPOUND SELECTED FROM THE GROUP CONSISTING OF PHENOL, RESORCINOL, XYLENOL AND CRESOL IN A MOLE RATIO OF ALKEHYDE TO PHENOLIC COMPOUND OF 0.5 : 1 TO 5 : 1 IN WATER IN AMOUNTS OF 25% TO 75% BASED ON THE TOTAL WEIGHT OF MATERIALS IN THE PRESENCE OF A CATALYST OF THE HYDROXIDE OR CARBONATE COMPOUNDS OF ALKALI METAL OR ALKALINE EARTH METALS, AMMONIUM HYDROXIDE OR AMMONIUM CARBONATE; FORMING A HIGHLY THERMOSETTABLE AND CROSS-LINKABLE ALDEHYDE CONDENSATION ALDEHYDE CONDENSATION PREPOLYMER HAVING A VISCOSITY OF 5 CPS TO 75 CPS AT 25*C, BY REACTING SAID ALDEHYDE WITH SAID PHENOLIC COMPOUND IN A MOLE RATIO OF ALDEHYDE TO PHENOLIC COMPOUND OF 2.0 : 1 TO 3.0 : 1 IN WATER IN AMOUNTS OF 25% TO 75% BASED ON THE TOTAL WEIGHT OF MATERIAL IN THE PRESENCE OF SAID CATALYST; ADMIXING FROM 90% - 10% BY WEIGHT OF SAID LINEAR ALDEHYDE PREPOLYMER WITH 10% - 90% BY WEIGHT OF SAID HIGHLY THERMOSETTABLE PREPOLYMER; AND COPOLYMERIZING SAID ADMIXING AT A TEMPERATURE OF 60*C TO THE REFLUX TEMPERATURE IN THE PRESENCE OF SAID BASE IN AMOUNTS OF 0.05 TO 00.8 MOLES PER MOLE OF PHENOLIC COMPOUND WHICH RESULTS IN A COPOLYMER HAVING A VISCOSITY OF 30 TO 3,000 CPS AT 25*C.
Claim 2
Independent Claim 257 words
A METHOD FOR FORMING AN ALDEHYDE-PHENOLIC CONDENSATION COPOLYMER, WHICH COMPRISES: FORMING AN ESSENTIALLY LINEAR AND NON-CROSS-LINKABLE ALDEHYDE CONDENSATION PREPOLYMER HAVING A VISCOSITY OF 5 CPS TO 75 CPS AT 25*C BY REACTING AN ALDEHYDE SELECTED FROM THE GROUP CONSISTING OF FORMALDEHYDE ACETALDEHYDE, BENZALKEHYDE, PROPIONALDEHYDE, BUTYRALDEHYDE, FURFURALDEHYDE, AND MIXTURES THEREOF WITH A PHENOLIC COMPOUND SELECTED FROM THE GROUP CONSISTING OF PHENOL, RESORCINOL, XYLENOL AND CRESOL IN A MOLE RATIO OF ALKEHYDE TO PHENOLIC COMPOUND OF 0.5 : 1 TO 5 : 1 IN WATER IN AMOUNTS OF 25% TO 75% BASED ON THE TOTAL WEIGHT OF MATERIALS IN THE PRESENCE OF A CATALYST OF THE HYDROXIDE OR CARBONATE COMPOUNDS OF ALKALI METAL OR ALKALINE EARTH METALS, AMMONIUM HYDROXIDE OR AMMONIUM CARBONATE; FORMING A HIGHLY THERMOSETTABLE AND CROSS-LINKABLE ALDEHYDE CONDENSATION ALDEHYDE CONDENSATION PREPOLYMER HAVING A VISCOSITY OF 5 CPS TO 75 CPS AT 25*C, BY REACTING SAID ALDEHYDE WITH SAID PHENOLIC COMPOUND IN A MOLE RATIO OF ALDEHYDE TO PHENOLIC COMPOUND OF 2.0 : 1 TO 3.0 : 1 IN WATER IN AMOUNTS OF 25% TO 75% BASED ON THE TOTAL WEIGHT OF MATERIAL IN THE PRESENCE OF SAID CATALYST; ADMIXING FROM 90% - 10% BY WEIGHT OF SAID LINEAR ALDEHYDE PREPOLYMER WITH 10% - 90% BY WEIGHT OF SAID HIGHLY THERMOSETTABLE PREPOLYMER; AND COPOLYMERIZING SAID ADMIXING AT A TEMPERATURE OF 60*C TO THE REFLUX TEMPERATURE IN THE PRESENCE OF SAID BASE IN AMOUNTS OF 0.05 TO 00.8 MOLES PER MOLE OF PHENOLIC COMPOUND WHICH RESULTS IN A COPOLYMER HAVING A VISCOSITY OF 30 TO 3,000 CPS AT 25*C.
Claim 3
Dependent Claim 30 words
The method of claim 1, wherein the mole ratio of said aldehyde to said phenolic compound in said highly thermosettable prepolymer ranges from 2.4 : 1 to 2.8 : 1.
Claim 4
Dependent Claim 12 words
The process of claim 1, wherein said prepolymers are phenolformaldehyde condensation polymers.
Claim 5
Independent Claim 232 words
A method for forming an aldehyde-phenolic condensation copolymer, which comprises the steps of: forming an essentially linear and non-cross-linkable aldehyde condensation prepolymer having a viscosity of 5 cps to 75 cps at 25*C by reacting an aldehyde selected from the group consisting of formaldehyde, acetaldehyde, benzaldehyde, propionaldehyde, butyraldehyde, furfuraldehyde, and mixtures thereof with a phenolic compound selected from the group consisting of phenol, resorcinol, xylenol and cresol in a mole ratio of aldehyde to phenolic compound of 0.5 : 1 to 1.5 : 1 in water in amounts of 25% to 75% based on the total weight of materials in the presence of a catalyst of the hydroxide or carbonate compounds of alkali metals or alkaline earth metals, ammonium hydroxide or ammonium carbonate; condensing from 90% - 10% by weight of said linear and non-cross-linkable aldehyde condensation prepolymer with 10% - 90% by weight of the components of a highly thermosettable and cross-linkable aldehyde condensation prepolymer of an aldehyde and a phenolic compound in the presence of said catalyst in 25% to 75% water based on the total weight of materials at a temperature less than 70*C until all of said aldehyde has reacted, wherein the mole ratio of said aldehyde and phenolic compound is 2.0 : 1 to 3.0 : 1; and continuing said condensation reaction until a copolymer is obtained having a viscosity of 30 to 3,000 cps at 25*C.
Claim 6
Independent Claim 232 words
A method for forming an aldehyde-phenolic condensation copolymer, which comprises the steps of: forming an essentially linear and non-cross-linkable aldehyde condensation prepolymer having a viscosity of 5 cps to 75 cps at 25*C by reacting an aldehyde selected from the group consisting of formaldehyde, acetaldehyde, benzaldehyde, propionaldehyde, butyraldehyde, furfuraldehyde, and mixtures thereof with a phenolic compound selected from the group consisting of phenol, resorcinol, xylenol and cresol in a mole ratio of aldehyde to phenolic compound of 0.5 : 1 to 1.5 : 1 in water in amounts of 25% to 75% based on the total weight of materials in the presence of a catalyst of the hydroxide or carbonate compounds of alkali metals or alkaline earth metals, ammonium hydroxide or ammonium carbonate; condensing from 90% - 10% by weight of said linear and non-cross-linkable aldehyde condensation prepolymer with 10% - 90% by weight of the components of a highly thermosettable and cross-linkable aldehyde condensation prepolymer of an aldehyde and a phenolic compound in the presence of said catalyst in 25% to 75% water based on the total weight of materials at a temperature less than 70*C until all of said aldehyde has reacted, wherein the mole ratio of said aldehyde and phenolic compound is 2.0 : 1 to 3.0 : 1; and continuing said condensation reaction until a copolymer is obtained having a viscosity of 30 to 3,000 cps at 25*C.
Claim 7
Independent Claim 227 words
A method of forming an aldehyde-phenolic condensation copolymer, which comprises tHe steps of: forming a highly thermosettable and cross-linkable aldehyde condensation prepolymer having a viscosity of 5 cps to 75 cps at 25*C by reacting an aldehyde selected from the group consisting of formaldehyde, acetaldehyde, benzaldehyde, propionaldehyde, butyraldehyde, furfuraldehyde and mixtures thereof with a phenolic compound selected from the group consisting of phenol, resorcinol, xylenol and cresol in a mole ratio of aldehyde to phenolic compound of 2.0 : 1 to 3.0 : 1 in water in amounts of 25% to 75% based on the total weight of materials in the presence of a catalyst of the hydroxide or carbonate compounds of alkali metals or alkaline earth metals, ammonium hydroxide or ammonium carbonate; condensing from 10% - 90% by weight of said highly thermosettable prepolymer with 90% - 10% by weight of the components of an essentially linear and non-cross-linkable aldehyde condensation prepolymer of an aldehyde and a phenolic compound in the presence of said catalyst in 25% to 75% water based on the total weight of materials at a temperature less than 70*C until all of said aldehyde has reacted, wherein the mole ratio of said aldehyde and phenolic compound is 0.5 to 1.5 : 1; and continuing said condensation reaction until a copolymer is obtained having a viscosity of 30 to 3,000 cps at 25*C.
Claim 8
Independent Claim 227 words
A method of forming an aldehyde-phenolic condensation copolymer, which comprises tHe steps of: forming a highly thermosettable and cross-linkable aldehyde condensation prepolymer having a viscosity of 5 cps to 75 cps at 25*C by reacting an aldehyde selected from the group consisting of formaldehyde, acetaldehyde, benzaldehyde, propionaldehyde, butyraldehyde, furfuraldehyde and mixtures thereof with a phenolic compound selected from the group consisting of phenol, resorcinol, xylenol and cresol in a mole ratio of aldehyde to phenolic compound of 2.0 : 1 to 3.0 : 1 in water in amounts of 25% to 75% based on the total weight of materials in the presence of a catalyst of the hydroxide or carbonate compounds of alkali metals or alkaline earth metals, ammonium hydroxide or ammonium carbonate; condensing from 10% - 90% by weight of said highly thermosettable prepolymer with 90% - 10% by weight of the components of an essentially linear and non-cross-linkable aldehyde condensation prepolymer of an aldehyde and a phenolic compound in the presence of said catalyst in 25% to 75% water based on the total weight of materials at a temperature less than 70*C until all of said aldehyde has reacted, wherein the mole ratio of said aldehyde and phenolic compound is 0.5 to 1.5 : 1; and continuing said condensation reaction until a copolymer is obtained having a viscosity of 30 to 3,000 cps at 25*C.

References Cited (Backward Citations)

US2456006A Cited
US2593926A Cited
US2631098A Cited
US2620288A Cited
US2620321A 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) 1978-12-15 1979-06-16 1979-12-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-12-15 1983-06-16 1983-12-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-12-15 1987-06-16 1987-12-16 $7700.00 Window Closed / Lapsed

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