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US4157324A Expired / Lapsed US ⏱️ 0.0 years remaining

High ortho etherified resole resins admixed with coreactive resins

Assignee: Hexion Inc
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Filing: 1978-06-29
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Granted: 1979-06-05
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Expires: 1998-06-29
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Abstract

Abstract This invention relates to high ortho etherified resole resins. The resole resins are prepared by reacting under acidic conditions phenol with formaldehyde in the presence of a divalent electropositive metal. The resole resins are then etherified with an alcohol and dehydrated to less than 1 percent water. The novel high ortho etherified resole resins are useful in coating, bonding and adhesive compositions. Such resoles are readily curable with coreactive resins providing chemical and solvent resistance.

Inventors

  • 👤 Harry M. Culbertson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 22:39
CPC Classifications
C; C08; C08G; C08G8/00; C08G8/28; C08G8/36; C08L; C08L61/00; C08L61/04; C08L61/06; C08L61/14; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31551; Y10T428/31627; Y10T428/31786; Y10T428/31942; Y10T428/31949; Y10T428/31964; Y10T428/31967

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 298 words
A high ortho etherified resole resin coating composition comprising a high ortho etherified resole resin and about 1 to 95% by weight of a coreactive resin, said high ortho etherified resole resin being characterized by: A. having a reacted formaldehyde to phenol mol ratio of 1.10 to 2.0, said formaldehyde reacting with said phenol, forming methylol groups taking a final orientation of about 90% to 100% in the ortho position, B. having said phenol selected from the group consisting of phenol, meta-substituted phenols and mixtures of phenol and substituted phenols, C. having condensed phenol-aldehyde linkages wherein 25 to 90% of said linkages are benzyl ether linkages having a final orientation essentially in the ortho position and 10 to 75% are methylene linkages taking a final orientation of about 70 to 90% in the ortho position and about 10 to 30% in the para position, D. having an average degree of polymerization of less than 4.0, and E. having said methylol groups partially etherified with monohydric alcohols, said etherified resoles being prepared by first reacting said phenol and said formaldehyde in an aqueous reaction mixture under reflux at about 80° C. to 100° C. in the presence of a divalent electropositive metal ion, while maintaining the pH in the range of about 4 to 7, wherein said pH is controlled by having a sufficient amount of an organic acid present, forming said resole in said reaction mixture, etherifying said resole with a monohydric alcohol at a temperature of 65° to 100° C., in said reaction mixture and dehydrating the resultant aqueous reaction mixture to a water content of less than about 1 weight percent and an alcohol content of less than about 5% by weight providing an etherified high ortho resole resin as a single phase clear liquid varnish.
Claim 2
Dependent Claim 298 words
A high ortho etherified resole resin coating composition comprising a high ortho etherified resole resin and about 1 to 95% by weight of a coreactive resin, said high ortho etherified resole resin being characterized by: A. having a reacted formaldehyde to phenol mol ratio of 1.10 to 2.0, said formaldehyde reacting with said phenol, forming methylol groups taking a final orientation of about 90% to 100% in the ortho position, B. having said phenol selected from the group consisting of phenol, meta-substituted phenols and mixtures of phenol and substituted phenols, C. having condensed phenol-aldehyde linkages wherein 25 to 90% of said linkages are benzyl ether linkages having a final orientation essentially in the ortho position and 10 to 75% are methylene linkages taking a final orientation of about 70 to 90% in the ortho position and about 10 to 30% in the para position, D. having an average degree of polymerization of less than 4.0, and E. having said methylol groups partially etherified with monohydric alcohols, said etherified resoles being prepared by first reacting said phenol and said formaldehyde in an aqueous reaction mixture under reflux at about 80° C. to 100° C. in the presence of a divalent electropositive metal ion, while maintaining the pH in the range of about 4 to 7, wherein said pH is controlled by having a sufficient amount of an organic acid present, forming said resole in said reaction mixture, etherifying said resole with a monohydric alcohol at a temperature of 65° to 100° C., in said reaction mixture and dehydrating the resultant aqueous reaction mixture to a water content of less than about 1 weight percent and an alcohol content of less than about 5% by weight providing an etherified high ortho resole resin as a single phase clear liquid varnish.
Claim 3
Dependent Claim 19 words
A coating composition of claim 1, said composition additionally containing a solvent for said resole and said coreactive resin.
Claim 4
Dependent Claim 25 words
A coating composition of claim 2 wherein said solvent is selected from the group consisting of lower alkanols, lower alkones or aromatic and aliphatic hydrocarbons.
Claim 5
Dependent Claim 33 words
A coating composition of claim 3 wherein said solvent is a solvent selected from the group consisting of ethanol, methanol, propanol, acetone, methyl ethyl ketone, benzene, toluene, xylene, naphthalene, nonene and petroleum fractions.
Claim 6
Dependent Claim 31 words
A composition of claim 1 wherein said coreactive resin contains coreactive functional groups selected from the group consisting of hydroxyl, carboxyl, amide, keto, methylol, isocyanate and alkoxymethyl, acetal or mixtures thereof.
Claim 7
Dependent Claim 35 words
A composition of claim 1 wherein said coreactive resin is selected from the group consisting of alkyl, epoxy, polyvinyl formal, polyvinyl butyral, polyester, polyvinyl acetate, polyvinyl alcohol, polyamide, polyurethane, polyether and polyacrylate and mixtures thereof.
Claim 8
Dependent Claim 34 words
A composition of claim 1 wherein said coreactive resin has a low molecular weight resin having a molecular weight of less than about 10,000 and about 80 to 98% of coating forming oligomeric components.
Claim 9
Dependent Claim 14 words
A coating composition of claim 1 having present a catalyst to cure said composition.
Claim 10
Dependent Claim 29 words
A coating composition of claim 8 wherein said catalyst is an acid selected from the group consisting of sulfonic, phosphoric, oxalic, acetic, adipic, succinic, lactic, benzoic or mixtures thereof.
Claim 11
Dependent Claim 38 words
A coating composition of claim 1 wherein said meta substituted phenol is a phenol having at least one attached radical selected from the group consisting of alkyd, aryl, cycloalkyl, alkenyl, cycloalkenyl, alkaryl, aralkyl, carbocyclic, halogen and mixtures thereof.
Claim 12
Dependent Claim 34 words
A coating composition of claim 1 wherein said substituted phenol is a phenol substituted with a material selected from the group consisting of indenes, vinylidene aromatics, cyclopentadienes, dicyclopentadienes, nonenes, octenes, terpenes and mixtures thereof.
Claim 13
Dependent Claim 69 words
A composition of claim 1 wherein said divalent electropositive metal ion is provided by a compound selected from the group consisting of oxides, hydroxides and organic acid salts of such metal ions, and wherein said resole resins are prepared in the presence of said compounds wherein the amount of said compound is within the range of about 0.1 to 10.0 weight percent based on the weight of said phenols.
Claim 14
Dependent Claim 32 words
A composition of claim 1 wherein said divalent electropositive metal ion is selected from the group consisting of zinc (Zn++), cobalt (Co+++), magnesium (Mg++), manganese (Mn++) and calcium (Ca++) or mixtures thereof.
Claim 15
Dependent Claim 19 words
A composition of claim 1 wherein the monohydric alcohol is selected from the group consisting of alkyl and aralkyl.
Claim 16
Dependent Claim 23 words
A composition of claim 1 wherein said alcohol is incorporated in amounts of about 0.05 to 0.50 methylol ether groups per phenolic group.

References Cited (Backward Citations)

GB773611A Cited
US3485797A Cited
US3637429A Cited
US3630977A Cited
CA927041A Cited
US4022942A Cited
US4017437A Cited
US4120847A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-06-04 1982-12-04 1983-06-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-06-04 1986-12-04 1987-06-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-06-04 1990-12-04 1991-06-05 $7700.00 Window Closed / Lapsed

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