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US3250734A Expired / Lapsed US ⏱️ 0.0 years remaining

Hydroxy interpolymers prepared from partially esterified carboxyl interpolymers and mono-1, 2-epoxides

Assignee: DESOTO CHEMICAL COATINGS Inc
•
Filing: 1962-10-10
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Granted: 1966-05-10
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Expires: 1982-10-10
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Abstract

No abstract record available.

Inventors

  • 👤 Sekmakas Kazys

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 09:21
CPC Classifications
C; C09; C09D; C09D135/00; C09D135/02; C08; C08F; C08F22/00; C08F22/04; C08F8/00; C08G; C08G63/00; C08G63/02; C08G63/12; C08G63/52; C08G63/56; C08G63/58; C09D167/00

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 156 words
A METHOD OF PRODUCING A STORAGE-STABLE, SOLVENTSOLUBLE NON-GELLED INTERPOLYMER CONTAINING A MALEIC ANHYDRIDE HYDROXY ESTER INTERPOLYMERIZED THEREIN COMPRISING, REACTING A PREFORMED ANHYDRIDE-CONTAINING ADDITION INTERPOLYMER OF A MALEIC ANHYDRIDE WITH ETHYLENICALLY UNSATURATED MATERIAL COPOLYMERIZABLE THEREWITH WITH MONOHYDRIC ALIPHATIC ORGANIC COMPOUND CONTAINING A SINGLE HYDROXYL GROUP AS THE SOLE FUNCTIONAL GROUP THEREOF TO PARTIALLY ESTERIFY ANHYDRIDE GROUPS AND THEREBY FORM SECONDARY CARBOXYL GROUPS, AND REACTING SAID SECONDARY CARBOXYL GROUPS IN THE PRESENCE OF EXCESS MONOHYDRIC ALIPHATIC ORGANIC COMPOUND WITH ORGANIC MONOEPOXIDE CONTAINING A SINGLE OXIRANE GROUP AS THE SOLE FUNCTIONAL GROUP THEREOF, SAID MONOHYDRIC COMPOUND BEING REACTED WITH SAID COPOLYMER TO AN EXTENT OF FROM 90-110% OF HALF ESTERIFICATION OF THE ANHYDRIDE GROUPS OF SAID COPOLYMER, AND SAID MONOEPOXIDE BEING REACTED WITH AT LEAST 20% OF THE SECONDARY CARBOXYL GROUPS MADE AVAILABLE BY REACTION WITH SAID MONOHYDRIC COMPOUND, SAID REACTIONS BEING CONDUCTED AT ELEVATED TEMPERATURE IN THE PRESENCE OF A CATALYTIC PROPORTION OF ALKALI METAL ORGANIC ACID SALT.
Claim 2
Independent Claim 156 words
A METHOD OF PRODUCING A STORAGE-STABLE, SOLVENTSOLUBLE NON-GELLED INTERPOLYMER CONTAINING A MALEIC ANHYDRIDE HYDROXY ESTER INTERPOLYMERIZED THEREIN COMPRISING, REACTING A PREFORMED ANHYDRIDE-CONTAINING ADDITION INTERPOLYMER OF A MALEIC ANHYDRIDE WITH ETHYLENICALLY UNSATURATED MATERIAL COPOLYMERIZABLE THEREWITH WITH MONOHYDRIC ALIPHATIC ORGANIC COMPOUND CONTAINING A SINGLE HYDROXYL GROUP AS THE SOLE FUNCTIONAL GROUP THEREOF TO PARTIALLY ESTERIFY ANHYDRIDE GROUPS AND THEREBY FORM SECONDARY CARBOXYL GROUPS, AND REACTING SAID SECONDARY CARBOXYL GROUPS IN THE PRESENCE OF EXCESS MONOHYDRIC ALIPHATIC ORGANIC COMPOUND WITH ORGANIC MONOEPOXIDE CONTAINING A SINGLE OXIRANE GROUP AS THE SOLE FUNCTIONAL GROUP THEREOF, SAID MONOHYDRIC COMPOUND BEING REACTED WITH SAID COPOLYMER TO AN EXTENT OF FROM 90-110% OF HALF ESTERIFICATION OF THE ANHYDRIDE GROUPS OF SAID COPOLYMER, AND SAID MONOEPOXIDE BEING REACTED WITH AT LEAST 20% OF THE SECONDARY CARBOXYL GROUPS MADE AVAILABLE BY REACTION WITH SAID MONOHYDRIC COMPOUND, SAID REACTIONS BEING CONDUCTED AT ELEVATED TEMPERATURE IN THE PRESENCE OF A CATALYTIC PROPORTION OF ALKALI METAL ORGANIC ACID SALT.

References Cited (Backward Citations)

US2681897A Cited
US3002959A Cited
US2961424A Cited
US2967162A Cited
US3136736A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1969-05-09 1969-11-08 1970-05-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1973-05-09 1973-11-08 1974-05-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1977-05-09 1977-11-08 1978-05-10 $7700.00 Window Closed / Lapsed

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